Intermolecular Forces - MCAT Biological and Biochemical Foundations of Living Systems
Card 1 of 40
Which intermolecular force accounts for the fact that alcohols have higher boiling points than alkanes?
Which intermolecular force accounts for the fact that alcohols have higher boiling points than alkanes?
Tap to reveal answer
Hydrogen bonding occurs when the hydrogen atom attached to an electronegative atom of one molecule (in an alcohol, this electronegative atom is oxygen) becomes attracted to an electronegative atom of a different molecule (either oxygen, nitrogen, or fluorine). This attractive force is so strong that it significantly increases the boiling point of the alcohol.
Hydrogen bonding occurs when the hydrogen atom attached to an electronegative atom of one molecule (in an alcohol, this electronegative atom is oxygen) becomes attracted to an electronegative atom of a different molecule (either oxygen, nitrogen, or fluorine). This attractive force is so strong that it significantly increases the boiling point of the alcohol.
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Prions are the suspected cause of a wide variety of neurodegenerative diseases in mammals. According to prevailing theory, prions are infectious particles made only of protein and found in high concentrations in the brains of infected animals. All mammals produce normal prion protein, PrPC, a transmembrane protein whose function remains unclear.
Infectious prions, PrPRes, induce conformational changes in the existing PrPC proteins according to the following reaction:
PrPC + PrPRes → PrPRes + PrPRes
The PrPRes is then suspected to accumulate in the nervous tissue of infected patients and cause disease. This model of transmission generates replicated proteins, but does so bypassing the standard model of the central dogma of molecular biology. Transcription and translation apparently do not play a role in this replication process.
This theory is a major departure from previously established biological dogma. A scientist decides to test the protein-only theory of prion propagation. He establishes his experiment as follows:
Homogenized brain matter of infected rabbits is injected into the brains of healthy rabbits, as per the following table:
Rabbit 1 and 2: injected with normal saline on days 1 and 2
The above trials serve as controls.
Rabbit 3 and 4: injected with homogenized brain matter on days 1 and 2
The above trials use unmodified brain matter.
Rabbit 5 and 6: injected with irradiated homogenized brain matter on days 1 and 2
The above trials use brain matter that has been irradiated to destroy nucleic acids in the homogenate.
Rabbit 7 and 8: injected with protein-free centrifuged homogenized brain matter on days 1 and 2
The above trials use brain matter that has been centrifuged to generate a protein-free homogenate and a protein-rich homogenate based on molecular weight.
Rabbit 9 and 10: injected with boiled homogenized brain matter on days 1 and 2
The above trials use brain matter that have been boiled to destroy any bacterial contaminants in the homogenate.
A scientist claims that he has discovered how PrPRes propagates. He claims that the PrPRes interacts with the PrPC by using its own partially negative oxygen atoms to interact with partially positive hydrogen atoms on PrPC. What is true of these bonds?
Prions are the suspected cause of a wide variety of neurodegenerative diseases in mammals. According to prevailing theory, prions are infectious particles made only of protein and found in high concentrations in the brains of infected animals. All mammals produce normal prion protein, PrPC, a transmembrane protein whose function remains unclear.
Infectious prions, PrPRes, induce conformational changes in the existing PrPC proteins according to the following reaction:
PrPC + PrPRes → PrPRes + PrPRes
The PrPRes is then suspected to accumulate in the nervous tissue of infected patients and cause disease. This model of transmission generates replicated proteins, but does so bypassing the standard model of the central dogma of molecular biology. Transcription and translation apparently do not play a role in this replication process.
This theory is a major departure from previously established biological dogma. A scientist decides to test the protein-only theory of prion propagation. He establishes his experiment as follows:
Homogenized brain matter of infected rabbits is injected into the brains of healthy rabbits, as per the following table:
Rabbit 1 and 2: injected with normal saline on days 1 and 2
The above trials serve as controls.
Rabbit 3 and 4: injected with homogenized brain matter on days 1 and 2
The above trials use unmodified brain matter.
Rabbit 5 and 6: injected with irradiated homogenized brain matter on days 1 and 2
The above trials use brain matter that has been irradiated to destroy nucleic acids in the homogenate.
Rabbit 7 and 8: injected with protein-free centrifuged homogenized brain matter on days 1 and 2
The above trials use brain matter that has been centrifuged to generate a protein-free homogenate and a protein-rich homogenate based on molecular weight.
Rabbit 9 and 10: injected with boiled homogenized brain matter on days 1 and 2
The above trials use brain matter that have been boiled to destroy any bacterial contaminants in the homogenate.
A scientist claims that he has discovered how PrPRes propagates. He claims that the PrPRes interacts with the PrPC by using its own partially negative oxygen atoms to interact with partially positive hydrogen atoms on PrPC. What is true of these bonds?
Tap to reveal answer
Hydrogen bonds are an example of the strongest type of intermolecular bonds. They are, however, still intermolecular, and thus always weaker than covalent bonds.
Hydrogen bonds are an example of the strongest type of intermolecular bonds. They are, however, still intermolecular, and thus always weaker than covalent bonds.
← Didn't Know|Knew It →
Cryptosporidium is a genus of gastrointestinal parasite that infects the intestinal epithelium of mammals. Cryptosporidium is water-borne, and is an apicomplexan parasite. This phylum also includes Plasmodium, Babesia, and Toxoplasma.
Apicomplexans are unique due to their apicoplast, an apical organelle that helps penetrate mammalian epithelium. In the case of cryptosporidium, there is an interaction between the surface proteins of mammalian epithelial tissue and those of the apical portion of the cryptosporidium infective stage, or oocyst. A scientist is conducting an experiment to test the hypothesis that the oocyst secretes a peptide compound that neutralizes intestinal defense cells. These defense cells are resident in the intestinal epithelium, and defend the tissue by phagocytizing the oocysts.
She sets up the following experiment:
As the neutralizing compound was believed to be secreted by the oocyst, the scientist collected oocysts onto growth media. The oocysts were grown among intestinal epithelial cells, and then the media was collected. The media was then added to another plate where Toxoplasma gondii was growing with intestinal epithelial cells. A second plate of Toxoplasma gondii was grown with the same type of intestinal epithelium, but no oocyst-sourced media was added.
A scientist is conducting a follow up experiment to the one described above. She is attempting to determine how cryptosporidium adheres to the gastrointestinal mucosa. She determines that the key step is a binding of a surface protein ligand to a receptor. Which of the following forces are common patterns for protein-protein interaction?
I. Hydrogen bonding
II. Coordinate covalent bonding
III. Polar covalent
IV. Metallic bonding
Cryptosporidium is a genus of gastrointestinal parasite that infects the intestinal epithelium of mammals. Cryptosporidium is water-borne, and is an apicomplexan parasite. This phylum also includes Plasmodium, Babesia, and Toxoplasma.
Apicomplexans are unique due to their apicoplast, an apical organelle that helps penetrate mammalian epithelium. In the case of cryptosporidium, there is an interaction between the surface proteins of mammalian epithelial tissue and those of the apical portion of the cryptosporidium infective stage, or oocyst. A scientist is conducting an experiment to test the hypothesis that the oocyst secretes a peptide compound that neutralizes intestinal defense cells. These defense cells are resident in the intestinal epithelium, and defend the tissue by phagocytizing the oocysts.
She sets up the following experiment:
As the neutralizing compound was believed to be secreted by the oocyst, the scientist collected oocysts onto growth media. The oocysts were grown among intestinal epithelial cells, and then the media was collected. The media was then added to another plate where Toxoplasma gondii was growing with intestinal epithelial cells. A second plate of Toxoplasma gondii was grown with the same type of intestinal epithelium, but no oocyst-sourced media was added.
A scientist is conducting a follow up experiment to the one described above. She is attempting to determine how cryptosporidium adheres to the gastrointestinal mucosa. She determines that the key step is a binding of a surface protein ligand to a receptor. Which of the following forces are common patterns for protein-protein interaction?
I. Hydrogen bonding
II. Coordinate covalent bonding
III. Polar covalent
IV. Metallic bonding
Tap to reveal answer
Of the choices listed, only hydrogen bonds would be very common among protein-protein bonds. Covalent bonds are strong and permanent, and so are uncommon between macromolecules. Some proteins form disulfide bridges, or covalent bonds between sulfur atoms intra-molecularly, but inter-molecularly covalent interactions are usually not appropriate.
Of the choices listed, only hydrogen bonds would be very common among protein-protein bonds. Covalent bonds are strong and permanent, and so are uncommon between macromolecules. Some proteins form disulfide bridges, or covalent bonds between sulfur atoms intra-molecularly, but inter-molecularly covalent interactions are usually not appropriate.
← Didn't Know|Knew It →
One component of the immune system is the neutrophil, a professional phagocyte that consumes invading cells. The neutrophil is ferried to the site of infection via the blood as pre-neutrophils, or monocytes, ready to differentiate as needed to defend their host.
In order to leave the blood and migrate to the tissues, where infection is active, the monocyte undergoes a process called diapedesis. Diapedesis is a process of extravasation, where the monocyte leaves the circulation by moving in between endothelial cells, enters the tissue, and matures into a neutrophil.
Diapedesis is mediated by a class of proteins called selectins, present on the monocyte membrane and the endothelium. These selectins interact, attract the monocyte to the endothelium, and allow the monocytes to roll along the endothelium until they are able to complete diapedesis by leaving the vasculature and entering the tissues.
The image below shows monocytes moving in the blood vessel, "rolling" along the vessel wall, and eventually leaving the vessel to migrate to the site of infection.
Which of the following is likely true about the interactions between selectins and the "rolling" monocytes?
One component of the immune system is the neutrophil, a professional phagocyte that consumes invading cells. The neutrophil is ferried to the site of infection via the blood as pre-neutrophils, or monocytes, ready to differentiate as needed to defend their host.
In order to leave the blood and migrate to the tissues, where infection is active, the monocyte undergoes a process called diapedesis. Diapedesis is a process of extravasation, where the monocyte leaves the circulation by moving in between endothelial cells, enters the tissue, and matures into a neutrophil.
Diapedesis is mediated by a class of proteins called selectins, present on the monocyte membrane and the endothelium. These selectins interact, attract the monocyte to the endothelium, and allow the monocytes to roll along the endothelium until they are able to complete diapedesis by leaving the vasculature and entering the tissues.
The image below shows monocytes moving in the blood vessel, "rolling" along the vessel wall, and eventually leaving the vessel to migrate to the site of infection.
Which of the following is likely true about the interactions between selectins and the "rolling" monocytes?
Tap to reveal answer
The interactions that give rise to the neutrophil rolling phenomenon are likely the product of intermolecular bonds, such as hydrogen bonds, that often do not require full ionic charges to be present.
Additionally, proteins and carbohydrates are the typical mediators of these interactions, not fatty acids, and they usually form quickly, reversibly, and spontaneously, without the help of local enzymes.
The interactions that give rise to the neutrophil rolling phenomenon are likely the product of intermolecular bonds, such as hydrogen bonds, that often do not require full ionic charges to be present.
Additionally, proteins and carbohydrates are the typical mediators of these interactions, not fatty acids, and they usually form quickly, reversibly, and spontaneously, without the help of local enzymes.
← Didn't Know|Knew It →
Type 1 diabetes is a well-understood autoimmune disease. Autoimmune diseases result from an immune system-mediated attack on one’s own body tissues. In normal development, an organ called the thymus introduces immune cells to the body’s normal proteins. This process is called negative selection, as those immune cells that recognize normal proteins are deleted. If cells evade this process, those that recognize normal proteins enter into circulation, where they can attack body tissues. The thymus is also important for activating T-cells that recognize foreign proteins.
As the figure below shows, immune cells typically originate in the bone marrow. Some immune cells, called T-cells, then go to the thymus for negative selection. Those that survive negative selection, enter into general circulation to fight infection. Other cells, called B-cells, directly enter general circulation from the bone marrow. It is a breakdown in this carefully orchestrated process that leads to autoimmune disease, such as type 1 diabetes.
In the process of negative selection described in the passage, the interaction of T-cells and normal body proteins happens via brief and easily broken biochemical bonds. What type of bonding is most probably involved?
Type 1 diabetes is a well-understood autoimmune disease. Autoimmune diseases result from an immune system-mediated attack on one’s own body tissues. In normal development, an organ called the thymus introduces immune cells to the body’s normal proteins. This process is called negative selection, as those immune cells that recognize normal proteins are deleted. If cells evade this process, those that recognize normal proteins enter into circulation, where they can attack body tissues. The thymus is also important for activating T-cells that recognize foreign proteins.
As the figure below shows, immune cells typically originate in the bone marrow. Some immune cells, called T-cells, then go to the thymus for negative selection. Those that survive negative selection, enter into general circulation to fight infection. Other cells, called B-cells, directly enter general circulation from the bone marrow. It is a breakdown in this carefully orchestrated process that leads to autoimmune disease, such as type 1 diabetes.
In the process of negative selection described in the passage, the interaction of T-cells and normal body proteins happens via brief and easily broken biochemical bonds. What type of bonding is most probably involved?
Tap to reveal answer
Hydrogen bonding is characteristic of a great deal of the intermolecular interactions seen in biochemical systems. Ionic and covalent bonding are far too permanent, and T-cells would never escape the thymus were these bonding patterns the principal interactions. Ionic and covalent interactions generally represent intramolecular interactions, while intermolecular interactions are more temporary. Common intermolecular forces are hydrogen bonding, dipole interactions, and van der Waals forces. (Note that hydrogen bonding can also be an intramolecular interaction for certain molecular structures).
Hydrogen bonding is characteristic of a great deal of the intermolecular interactions seen in biochemical systems. Ionic and covalent bonding are far too permanent, and T-cells would never escape the thymus were these bonding patterns the principal interactions. Ionic and covalent interactions generally represent intramolecular interactions, while intermolecular interactions are more temporary. Common intermolecular forces are hydrogen bonding, dipole interactions, and van der Waals forces. (Note that hydrogen bonding can also be an intramolecular interaction for certain molecular structures).
← Didn't Know|Knew It →
Prions are the suspected cause of a wide variety of neurodegenerative diseases in mammals. According to prevailing theory, prions are infectious particles made only of protein and found in high concentrations in the brains of infected animals. All mammals produce normal prion protein, PrPC, a transmembrane protein whose function remains unclear.
Infectious prions, PrPRes, induce conformational changes in the existing PrPC proteins according to the following reaction:
PrPC + PrPRes → PrPRes + PrPRes
The PrPRes is then suspected to accumulate in the nervous tissue of infected patients and cause disease. This model of transmission generates replicated proteins, but does so bypassing the standard model of the central dogma of molecular biology. Transcription and translation apparently do not play a role in this replication process.
This theory is a major departure from previously established biological dogma. A scientist decides to test the protein-only theory of prion propagation. He establishes his experiment as follows:
Homogenized brain matter of infected rabbits is injected into the brains of healthy rabbits, as per the following table:
Rabbit 1 and 2: injected with normal saline on days 1 and 2
The above trials serve as controls.
Rabbit 3 and 4: injected with homogenized brain matter on days 1 and 2
The above trials use unmodified brain matter.
Rabbit 5 and 6: injected with irradiated homogenized brain matter on days 1 and 2
The above trials use brain matter that has been irradiated to destroy nucleic acids in the homogenate.
Rabbit 7 and 8: injected with protein-free centrifuged homogenized brain matter on days 1 and 2
The above trials use brain matter that has been centrifuged to generate a protein-free homogenate and a protein-rich homogenate based on molecular weight.
Rabbit 9 and 10: injected with boiled homogenized brain matter on days 1 and 2
The above trials use brain matter that have been boiled to destroy any bacterial contaminants in the homogenate.
A scientist claims that he has discovered how PrPRes propagates. He claims that the PrPRes interacts with the PrPC by using its own partially negative oxygen atoms to interact with partially positive hydrogen atoms on PrPC. What is true of these bonds?
Prions are the suspected cause of a wide variety of neurodegenerative diseases in mammals. According to prevailing theory, prions are infectious particles made only of protein and found in high concentrations in the brains of infected animals. All mammals produce normal prion protein, PrPC, a transmembrane protein whose function remains unclear.
Infectious prions, PrPRes, induce conformational changes in the existing PrPC proteins according to the following reaction:
PrPC + PrPRes → PrPRes + PrPRes
The PrPRes is then suspected to accumulate in the nervous tissue of infected patients and cause disease. This model of transmission generates replicated proteins, but does so bypassing the standard model of the central dogma of molecular biology. Transcription and translation apparently do not play a role in this replication process.
This theory is a major departure from previously established biological dogma. A scientist decides to test the protein-only theory of prion propagation. He establishes his experiment as follows:
Homogenized brain matter of infected rabbits is injected into the brains of healthy rabbits, as per the following table:
Rabbit 1 and 2: injected with normal saline on days 1 and 2
The above trials serve as controls.
Rabbit 3 and 4: injected with homogenized brain matter on days 1 and 2
The above trials use unmodified brain matter.
Rabbit 5 and 6: injected with irradiated homogenized brain matter on days 1 and 2
The above trials use brain matter that has been irradiated to destroy nucleic acids in the homogenate.
Rabbit 7 and 8: injected with protein-free centrifuged homogenized brain matter on days 1 and 2
The above trials use brain matter that has been centrifuged to generate a protein-free homogenate and a protein-rich homogenate based on molecular weight.
Rabbit 9 and 10: injected with boiled homogenized brain matter on days 1 and 2
The above trials use brain matter that have been boiled to destroy any bacterial contaminants in the homogenate.
A scientist claims that he has discovered how PrPRes propagates. He claims that the PrPRes interacts with the PrPC by using its own partially negative oxygen atoms to interact with partially positive hydrogen atoms on PrPC. What is true of these bonds?
Tap to reveal answer
Hydrogen bonds are an example of the strongest type of intermolecular bonds. They are, however, still intermolecular, and thus always weaker than covalent bonds.
Hydrogen bonds are an example of the strongest type of intermolecular bonds. They are, however, still intermolecular, and thus always weaker than covalent bonds.
← Didn't Know|Knew It →
Cryptosporidium is a genus of gastrointestinal parasite that infects the intestinal epithelium of mammals. Cryptosporidium is water-borne, and is an apicomplexan parasite. This phylum also includes Plasmodium, Babesia, and Toxoplasma.
Apicomplexans are unique due to their apicoplast, an apical organelle that helps penetrate mammalian epithelium. In the case of cryptosporidium, there is an interaction between the surface proteins of mammalian epithelial tissue and those of the apical portion of the cryptosporidium infective stage, or oocyst. A scientist is conducting an experiment to test the hypothesis that the oocyst secretes a peptide compound that neutralizes intestinal defense cells. These defense cells are resident in the intestinal epithelium, and defend the tissue by phagocytizing the oocysts.
She sets up the following experiment:
As the neutralizing compound was believed to be secreted by the oocyst, the scientist collected oocysts onto growth media. The oocysts were grown among intestinal epithelial cells, and then the media was collected. The media was then added to another plate where Toxoplasma gondii was growing with intestinal epithelial cells. A second plate of Toxoplasma gondii was grown with the same type of intestinal epithelium, but no oocyst-sourced media was added.
A scientist is conducting a follow up experiment to the one described above. She is attempting to determine how cryptosporidium adheres to the gastrointestinal mucosa. She determines that the key step is a binding of a surface protein ligand to a receptor. Which of the following forces are common patterns for protein-protein interaction?
I. Hydrogen bonding
II. Coordinate covalent bonding
III. Polar covalent
IV. Metallic bonding
Cryptosporidium is a genus of gastrointestinal parasite that infects the intestinal epithelium of mammals. Cryptosporidium is water-borne, and is an apicomplexan parasite. This phylum also includes Plasmodium, Babesia, and Toxoplasma.
Apicomplexans are unique due to their apicoplast, an apical organelle that helps penetrate mammalian epithelium. In the case of cryptosporidium, there is an interaction between the surface proteins of mammalian epithelial tissue and those of the apical portion of the cryptosporidium infective stage, or oocyst. A scientist is conducting an experiment to test the hypothesis that the oocyst secretes a peptide compound that neutralizes intestinal defense cells. These defense cells are resident in the intestinal epithelium, and defend the tissue by phagocytizing the oocysts.
She sets up the following experiment:
As the neutralizing compound was believed to be secreted by the oocyst, the scientist collected oocysts onto growth media. The oocysts were grown among intestinal epithelial cells, and then the media was collected. The media was then added to another plate where Toxoplasma gondii was growing with intestinal epithelial cells. A second plate of Toxoplasma gondii was grown with the same type of intestinal epithelium, but no oocyst-sourced media was added.
A scientist is conducting a follow up experiment to the one described above. She is attempting to determine how cryptosporidium adheres to the gastrointestinal mucosa. She determines that the key step is a binding of a surface protein ligand to a receptor. Which of the following forces are common patterns for protein-protein interaction?
I. Hydrogen bonding
II. Coordinate covalent bonding
III. Polar covalent
IV. Metallic bonding
Tap to reveal answer
Of the choices listed, only hydrogen bonds would be very common among protein-protein bonds. Covalent bonds are strong and permanent, and so are uncommon between macromolecules. Some proteins form disulfide bridges, or covalent bonds between sulfur atoms intra-molecularly, but inter-molecularly covalent interactions are usually not appropriate.
Of the choices listed, only hydrogen bonds would be very common among protein-protein bonds. Covalent bonds are strong and permanent, and so are uncommon between macromolecules. Some proteins form disulfide bridges, or covalent bonds between sulfur atoms intra-molecularly, but inter-molecularly covalent interactions are usually not appropriate.
← Didn't Know|Knew It →
One component of the immune system is the neutrophil, a professional phagocyte that consumes invading cells. The neutrophil is ferried to the site of infection via the blood as pre-neutrophils, or monocytes, ready to differentiate as needed to defend their host.
In order to leave the blood and migrate to the tissues, where infection is active, the monocyte undergoes a process called diapedesis. Diapedesis is a process of extravasation, where the monocyte leaves the circulation by moving in between endothelial cells, enters the tissue, and matures into a neutrophil.
Diapedesis is mediated by a class of proteins called selectins, present on the monocyte membrane and the endothelium. These selectins interact, attract the monocyte to the endothelium, and allow the monocytes to roll along the endothelium until they are able to complete diapedesis by leaving the vasculature and entering the tissues.
The image below shows monocytes moving in the blood vessel, "rolling" along the vessel wall, and eventually leaving the vessel to migrate to the site of infection.
Which of the following is likely true about the interactions between selectins and the "rolling" monocytes?
One component of the immune system is the neutrophil, a professional phagocyte that consumes invading cells. The neutrophil is ferried to the site of infection via the blood as pre-neutrophils, or monocytes, ready to differentiate as needed to defend their host.
In order to leave the blood and migrate to the tissues, where infection is active, the monocyte undergoes a process called diapedesis. Diapedesis is a process of extravasation, where the monocyte leaves the circulation by moving in between endothelial cells, enters the tissue, and matures into a neutrophil.
Diapedesis is mediated by a class of proteins called selectins, present on the monocyte membrane and the endothelium. These selectins interact, attract the monocyte to the endothelium, and allow the monocytes to roll along the endothelium until they are able to complete diapedesis by leaving the vasculature and entering the tissues.
The image below shows monocytes moving in the blood vessel, "rolling" along the vessel wall, and eventually leaving the vessel to migrate to the site of infection.
Which of the following is likely true about the interactions between selectins and the "rolling" monocytes?
Tap to reveal answer
The interactions that give rise to the neutrophil rolling phenomenon are likely the product of intermolecular bonds, such as hydrogen bonds, that often do not require full ionic charges to be present.
Additionally, proteins and carbohydrates are the typical mediators of these interactions, not fatty acids, and they usually form quickly, reversibly, and spontaneously, without the help of local enzymes.
The interactions that give rise to the neutrophil rolling phenomenon are likely the product of intermolecular bonds, such as hydrogen bonds, that often do not require full ionic charges to be present.
Additionally, proteins and carbohydrates are the typical mediators of these interactions, not fatty acids, and they usually form quickly, reversibly, and spontaneously, without the help of local enzymes.
← Didn't Know|Knew It →
Type 1 diabetes is a well-understood autoimmune disease. Autoimmune diseases result from an immune system-mediated attack on one’s own body tissues. In normal development, an organ called the thymus introduces immune cells to the body’s normal proteins. This process is called negative selection, as those immune cells that recognize normal proteins are deleted. If cells evade this process, those that recognize normal proteins enter into circulation, where they can attack body tissues. The thymus is also important for activating T-cells that recognize foreign proteins.
As the figure below shows, immune cells typically originate in the bone marrow. Some immune cells, called T-cells, then go to the thymus for negative selection. Those that survive negative selection, enter into general circulation to fight infection. Other cells, called B-cells, directly enter general circulation from the bone marrow. It is a breakdown in this carefully orchestrated process that leads to autoimmune disease, such as type 1 diabetes.
In the process of negative selection described in the passage, the interaction of T-cells and normal body proteins happens via brief and easily broken biochemical bonds. What type of bonding is most probably involved?
Type 1 diabetes is a well-understood autoimmune disease. Autoimmune diseases result from an immune system-mediated attack on one’s own body tissues. In normal development, an organ called the thymus introduces immune cells to the body’s normal proteins. This process is called negative selection, as those immune cells that recognize normal proteins are deleted. If cells evade this process, those that recognize normal proteins enter into circulation, where they can attack body tissues. The thymus is also important for activating T-cells that recognize foreign proteins.
As the figure below shows, immune cells typically originate in the bone marrow. Some immune cells, called T-cells, then go to the thymus for negative selection. Those that survive negative selection, enter into general circulation to fight infection. Other cells, called B-cells, directly enter general circulation from the bone marrow. It is a breakdown in this carefully orchestrated process that leads to autoimmune disease, such as type 1 diabetes.
In the process of negative selection described in the passage, the interaction of T-cells and normal body proteins happens via brief and easily broken biochemical bonds. What type of bonding is most probably involved?
Tap to reveal answer
Hydrogen bonding is characteristic of a great deal of the intermolecular interactions seen in biochemical systems. Ionic and covalent bonding are far too permanent, and T-cells would never escape the thymus were these bonding patterns the principal interactions. Ionic and covalent interactions generally represent intramolecular interactions, while intermolecular interactions are more temporary. Common intermolecular forces are hydrogen bonding, dipole interactions, and van der Waals forces. (Note that hydrogen bonding can also be an intramolecular interaction for certain molecular structures).
Hydrogen bonding is characteristic of a great deal of the intermolecular interactions seen in biochemical systems. Ionic and covalent bonding are far too permanent, and T-cells would never escape the thymus were these bonding patterns the principal interactions. Ionic and covalent interactions generally represent intramolecular interactions, while intermolecular interactions are more temporary. Common intermolecular forces are hydrogen bonding, dipole interactions, and van der Waals forces. (Note that hydrogen bonding can also be an intramolecular interaction for certain molecular structures).
← Didn't Know|Knew It →
Which intermolecular force accounts for the fact that alcohols have higher boiling points than alkanes?
Which intermolecular force accounts for the fact that alcohols have higher boiling points than alkanes?
Tap to reveal answer
Hydrogen bonding occurs when the hydrogen atom attached to an electronegative atom of one molecule (in an alcohol, this electronegative atom is oxygen) becomes attracted to an electronegative atom of a different molecule (either oxygen, nitrogen, or fluorine). This attractive force is so strong that it significantly increases the boiling point of the alcohol.
Hydrogen bonding occurs when the hydrogen atom attached to an electronegative atom of one molecule (in an alcohol, this electronegative atom is oxygen) becomes attracted to an electronegative atom of a different molecule (either oxygen, nitrogen, or fluorine). This attractive force is so strong that it significantly increases the boiling point of the alcohol.
← Didn't Know|Knew It →
Prions are the suspected cause of a wide variety of neurodegenerative diseases in mammals. According to prevailing theory, prions are infectious particles made only of protein and found in high concentrations in the brains of infected animals. All mammals produce normal prion protein, PrPC, a transmembrane protein whose function remains unclear.
Infectious prions, PrPRes, induce conformational changes in the existing PrPC proteins according to the following reaction:
PrPC + PrPRes → PrPRes + PrPRes
The PrPRes is then suspected to accumulate in the nervous tissue of infected patients and cause disease. This model of transmission generates replicated proteins, but does so bypassing the standard model of the central dogma of molecular biology. Transcription and translation apparently do not play a role in this replication process.
This theory is a major departure from previously established biological dogma. A scientist decides to test the protein-only theory of prion propagation. He establishes his experiment as follows:
Homogenized brain matter of infected rabbits is injected into the brains of healthy rabbits, as per the following table:
Rabbit 1 and 2: injected with normal saline on days 1 and 2
The above trials serve as controls.
Rabbit 3 and 4: injected with homogenized brain matter on days 1 and 2
The above trials use unmodified brain matter.
Rabbit 5 and 6: injected with irradiated homogenized brain matter on days 1 and 2
The above trials use brain matter that has been irradiated to destroy nucleic acids in the homogenate.
Rabbit 7 and 8: injected with protein-free centrifuged homogenized brain matter on days 1 and 2
The above trials use brain matter that has been centrifuged to generate a protein-free homogenate and a protein-rich homogenate based on molecular weight.
Rabbit 9 and 10: injected with boiled homogenized brain matter on days 1 and 2
The above trials use brain matter that have been boiled to destroy any bacterial contaminants in the homogenate.
A scientist claims that he has discovered how PrPRes propagates. He claims that the PrPRes interacts with the PrPC by using its own partially negative oxygen atoms to interact with partially positive hydrogen atoms on PrPC. What is true of these bonds?
Prions are the suspected cause of a wide variety of neurodegenerative diseases in mammals. According to prevailing theory, prions are infectious particles made only of protein and found in high concentrations in the brains of infected animals. All mammals produce normal prion protein, PrPC, a transmembrane protein whose function remains unclear.
Infectious prions, PrPRes, induce conformational changes in the existing PrPC proteins according to the following reaction:
PrPC + PrPRes → PrPRes + PrPRes
The PrPRes is then suspected to accumulate in the nervous tissue of infected patients and cause disease. This model of transmission generates replicated proteins, but does so bypassing the standard model of the central dogma of molecular biology. Transcription and translation apparently do not play a role in this replication process.
This theory is a major departure from previously established biological dogma. A scientist decides to test the protein-only theory of prion propagation. He establishes his experiment as follows:
Homogenized brain matter of infected rabbits is injected into the brains of healthy rabbits, as per the following table:
Rabbit 1 and 2: injected with normal saline on days 1 and 2
The above trials serve as controls.
Rabbit 3 and 4: injected with homogenized brain matter on days 1 and 2
The above trials use unmodified brain matter.
Rabbit 5 and 6: injected with irradiated homogenized brain matter on days 1 and 2
The above trials use brain matter that has been irradiated to destroy nucleic acids in the homogenate.
Rabbit 7 and 8: injected with protein-free centrifuged homogenized brain matter on days 1 and 2
The above trials use brain matter that has been centrifuged to generate a protein-free homogenate and a protein-rich homogenate based on molecular weight.
Rabbit 9 and 10: injected with boiled homogenized brain matter on days 1 and 2
The above trials use brain matter that have been boiled to destroy any bacterial contaminants in the homogenate.
A scientist claims that he has discovered how PrPRes propagates. He claims that the PrPRes interacts with the PrPC by using its own partially negative oxygen atoms to interact with partially positive hydrogen atoms on PrPC. What is true of these bonds?
Tap to reveal answer
Hydrogen bonds are an example of the strongest type of intermolecular bonds. They are, however, still intermolecular, and thus always weaker than covalent bonds.
Hydrogen bonds are an example of the strongest type of intermolecular bonds. They are, however, still intermolecular, and thus always weaker than covalent bonds.
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Cryptosporidium is a genus of gastrointestinal parasite that infects the intestinal epithelium of mammals. Cryptosporidium is water-borne, and is an apicomplexan parasite. This phylum also includes Plasmodium, Babesia, and Toxoplasma.
Apicomplexans are unique due to their apicoplast, an apical organelle that helps penetrate mammalian epithelium. In the case of cryptosporidium, there is an interaction between the surface proteins of mammalian epithelial tissue and those of the apical portion of the cryptosporidium infective stage, or oocyst. A scientist is conducting an experiment to test the hypothesis that the oocyst secretes a peptide compound that neutralizes intestinal defense cells. These defense cells are resident in the intestinal epithelium, and defend the tissue by phagocytizing the oocysts.
She sets up the following experiment:
As the neutralizing compound was believed to be secreted by the oocyst, the scientist collected oocysts onto growth media. The oocysts were grown among intestinal epithelial cells, and then the media was collected. The media was then added to another plate where Toxoplasma gondii was growing with intestinal epithelial cells. A second plate of Toxoplasma gondii was grown with the same type of intestinal epithelium, but no oocyst-sourced media was added.
A scientist is conducting a follow up experiment to the one described above. She is attempting to determine how cryptosporidium adheres to the gastrointestinal mucosa. She determines that the key step is a binding of a surface protein ligand to a receptor. Which of the following forces are common patterns for protein-protein interaction?
I. Hydrogen bonding
II. Coordinate covalent bonding
III. Polar covalent
IV. Metallic bonding
Cryptosporidium is a genus of gastrointestinal parasite that infects the intestinal epithelium of mammals. Cryptosporidium is water-borne, and is an apicomplexan parasite. This phylum also includes Plasmodium, Babesia, and Toxoplasma.
Apicomplexans are unique due to their apicoplast, an apical organelle that helps penetrate mammalian epithelium. In the case of cryptosporidium, there is an interaction between the surface proteins of mammalian epithelial tissue and those of the apical portion of the cryptosporidium infective stage, or oocyst. A scientist is conducting an experiment to test the hypothesis that the oocyst secretes a peptide compound that neutralizes intestinal defense cells. These defense cells are resident in the intestinal epithelium, and defend the tissue by phagocytizing the oocysts.
She sets up the following experiment:
As the neutralizing compound was believed to be secreted by the oocyst, the scientist collected oocysts onto growth media. The oocysts were grown among intestinal epithelial cells, and then the media was collected. The media was then added to another plate where Toxoplasma gondii was growing with intestinal epithelial cells. A second plate of Toxoplasma gondii was grown with the same type of intestinal epithelium, but no oocyst-sourced media was added.
A scientist is conducting a follow up experiment to the one described above. She is attempting to determine how cryptosporidium adheres to the gastrointestinal mucosa. She determines that the key step is a binding of a surface protein ligand to a receptor. Which of the following forces are common patterns for protein-protein interaction?
I. Hydrogen bonding
II. Coordinate covalent bonding
III. Polar covalent
IV. Metallic bonding
Tap to reveal answer
Of the choices listed, only hydrogen bonds would be very common among protein-protein bonds. Covalent bonds are strong and permanent, and so are uncommon between macromolecules. Some proteins form disulfide bridges, or covalent bonds between sulfur atoms intra-molecularly, but inter-molecularly covalent interactions are usually not appropriate.
Of the choices listed, only hydrogen bonds would be very common among protein-protein bonds. Covalent bonds are strong and permanent, and so are uncommon between macromolecules. Some proteins form disulfide bridges, or covalent bonds between sulfur atoms intra-molecularly, but inter-molecularly covalent interactions are usually not appropriate.
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One component of the immune system is the neutrophil, a professional phagocyte that consumes invading cells. The neutrophil is ferried to the site of infection via the blood as pre-neutrophils, or monocytes, ready to differentiate as needed to defend their host.
In order to leave the blood and migrate to the tissues, where infection is active, the monocyte undergoes a process called diapedesis. Diapedesis is a process of extravasation, where the monocyte leaves the circulation by moving in between endothelial cells, enters the tissue, and matures into a neutrophil.
Diapedesis is mediated by a class of proteins called selectins, present on the monocyte membrane and the endothelium. These selectins interact, attract the monocyte to the endothelium, and allow the monocytes to roll along the endothelium until they are able to complete diapedesis by leaving the vasculature and entering the tissues.
The image below shows monocytes moving in the blood vessel, "rolling" along the vessel wall, and eventually leaving the vessel to migrate to the site of infection.
Which of the following is likely true about the interactions between selectins and the "rolling" monocytes?
One component of the immune system is the neutrophil, a professional phagocyte that consumes invading cells. The neutrophil is ferried to the site of infection via the blood as pre-neutrophils, or monocytes, ready to differentiate as needed to defend their host.
In order to leave the blood and migrate to the tissues, where infection is active, the monocyte undergoes a process called diapedesis. Diapedesis is a process of extravasation, where the monocyte leaves the circulation by moving in between endothelial cells, enters the tissue, and matures into a neutrophil.
Diapedesis is mediated by a class of proteins called selectins, present on the monocyte membrane and the endothelium. These selectins interact, attract the monocyte to the endothelium, and allow the monocytes to roll along the endothelium until they are able to complete diapedesis by leaving the vasculature and entering the tissues.
The image below shows monocytes moving in the blood vessel, "rolling" along the vessel wall, and eventually leaving the vessel to migrate to the site of infection.
Which of the following is likely true about the interactions between selectins and the "rolling" monocytes?
Tap to reveal answer
The interactions that give rise to the neutrophil rolling phenomenon are likely the product of intermolecular bonds, such as hydrogen bonds, that often do not require full ionic charges to be present.
Additionally, proteins and carbohydrates are the typical mediators of these interactions, not fatty acids, and they usually form quickly, reversibly, and spontaneously, without the help of local enzymes.
The interactions that give rise to the neutrophil rolling phenomenon are likely the product of intermolecular bonds, such as hydrogen bonds, that often do not require full ionic charges to be present.
Additionally, proteins and carbohydrates are the typical mediators of these interactions, not fatty acids, and they usually form quickly, reversibly, and spontaneously, without the help of local enzymes.
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Type 1 diabetes is a well-understood autoimmune disease. Autoimmune diseases result from an immune system-mediated attack on one’s own body tissues. In normal development, an organ called the thymus introduces immune cells to the body’s normal proteins. This process is called negative selection, as those immune cells that recognize normal proteins are deleted. If cells evade this process, those that recognize normal proteins enter into circulation, where they can attack body tissues. The thymus is also important for activating T-cells that recognize foreign proteins.
As the figure below shows, immune cells typically originate in the bone marrow. Some immune cells, called T-cells, then go to the thymus for negative selection. Those that survive negative selection, enter into general circulation to fight infection. Other cells, called B-cells, directly enter general circulation from the bone marrow. It is a breakdown in this carefully orchestrated process that leads to autoimmune disease, such as type 1 diabetes.
In the process of negative selection described in the passage, the interaction of T-cells and normal body proteins happens via brief and easily broken biochemical bonds. What type of bonding is most probably involved?
Type 1 diabetes is a well-understood autoimmune disease. Autoimmune diseases result from an immune system-mediated attack on one’s own body tissues. In normal development, an organ called the thymus introduces immune cells to the body’s normal proteins. This process is called negative selection, as those immune cells that recognize normal proteins are deleted. If cells evade this process, those that recognize normal proteins enter into circulation, where they can attack body tissues. The thymus is also important for activating T-cells that recognize foreign proteins.
As the figure below shows, immune cells typically originate in the bone marrow. Some immune cells, called T-cells, then go to the thymus for negative selection. Those that survive negative selection, enter into general circulation to fight infection. Other cells, called B-cells, directly enter general circulation from the bone marrow. It is a breakdown in this carefully orchestrated process that leads to autoimmune disease, such as type 1 diabetes.
In the process of negative selection described in the passage, the interaction of T-cells and normal body proteins happens via brief and easily broken biochemical bonds. What type of bonding is most probably involved?
Tap to reveal answer
Hydrogen bonding is characteristic of a great deal of the intermolecular interactions seen in biochemical systems. Ionic and covalent bonding are far too permanent, and T-cells would never escape the thymus were these bonding patterns the principal interactions. Ionic and covalent interactions generally represent intramolecular interactions, while intermolecular interactions are more temporary. Common intermolecular forces are hydrogen bonding, dipole interactions, and van der Waals forces. (Note that hydrogen bonding can also be an intramolecular interaction for certain molecular structures).
Hydrogen bonding is characteristic of a great deal of the intermolecular interactions seen in biochemical systems. Ionic and covalent bonding are far too permanent, and T-cells would never escape the thymus were these bonding patterns the principal interactions. Ionic and covalent interactions generally represent intramolecular interactions, while intermolecular interactions are more temporary. Common intermolecular forces are hydrogen bonding, dipole interactions, and van der Waals forces. (Note that hydrogen bonding can also be an intramolecular interaction for certain molecular structures).
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Which intermolecular force accounts for the fact that alcohols have higher boiling points than alkanes?
Which intermolecular force accounts for the fact that alcohols have higher boiling points than alkanes?
Tap to reveal answer
Hydrogen bonding occurs when the hydrogen atom attached to an electronegative atom of one molecule (in an alcohol, this electronegative atom is oxygen) becomes attracted to an electronegative atom of a different molecule (either oxygen, nitrogen, or fluorine). This attractive force is so strong that it significantly increases the boiling point of the alcohol.
Hydrogen bonding occurs when the hydrogen atom attached to an electronegative atom of one molecule (in an alcohol, this electronegative atom is oxygen) becomes attracted to an electronegative atom of a different molecule (either oxygen, nitrogen, or fluorine). This attractive force is so strong that it significantly increases the boiling point of the alcohol.
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Prions are the suspected cause of a wide variety of neurodegenerative diseases in mammals. According to prevailing theory, prions are infectious particles made only of protein and found in high concentrations in the brains of infected animals. All mammals produce normal prion protein, PrPC, a transmembrane protein whose function remains unclear.
Infectious prions, PrPRes, induce conformational changes in the existing PrPC proteins according to the following reaction:
PrPC + PrPRes → PrPRes + PrPRes
The PrPRes is then suspected to accumulate in the nervous tissue of infected patients and cause disease. This model of transmission generates replicated proteins, but does so bypassing the standard model of the central dogma of molecular biology. Transcription and translation apparently do not play a role in this replication process.
This theory is a major departure from previously established biological dogma. A scientist decides to test the protein-only theory of prion propagation. He establishes his experiment as follows:
Homogenized brain matter of infected rabbits is injected into the brains of healthy rabbits, as per the following table:
Rabbit 1 and 2: injected with normal saline on days 1 and 2
The above trials serve as controls.
Rabbit 3 and 4: injected with homogenized brain matter on days 1 and 2
The above trials use unmodified brain matter.
Rabbit 5 and 6: injected with irradiated homogenized brain matter on days 1 and 2
The above trials use brain matter that has been irradiated to destroy nucleic acids in the homogenate.
Rabbit 7 and 8: injected with protein-free centrifuged homogenized brain matter on days 1 and 2
The above trials use brain matter that has been centrifuged to generate a protein-free homogenate and a protein-rich homogenate based on molecular weight.
Rabbit 9 and 10: injected with boiled homogenized brain matter on days 1 and 2
The above trials use brain matter that have been boiled to destroy any bacterial contaminants in the homogenate.
A scientist claims that he has discovered how PrPRes propagates. He claims that the PrPRes interacts with the PrPC by using its own partially negative oxygen atoms to interact with partially positive hydrogen atoms on PrPC. What is true of these bonds?
Prions are the suspected cause of a wide variety of neurodegenerative diseases in mammals. According to prevailing theory, prions are infectious particles made only of protein and found in high concentrations in the brains of infected animals. All mammals produce normal prion protein, PrPC, a transmembrane protein whose function remains unclear.
Infectious prions, PrPRes, induce conformational changes in the existing PrPC proteins according to the following reaction:
PrPC + PrPRes → PrPRes + PrPRes
The PrPRes is then suspected to accumulate in the nervous tissue of infected patients and cause disease. This model of transmission generates replicated proteins, but does so bypassing the standard model of the central dogma of molecular biology. Transcription and translation apparently do not play a role in this replication process.
This theory is a major departure from previously established biological dogma. A scientist decides to test the protein-only theory of prion propagation. He establishes his experiment as follows:
Homogenized brain matter of infected rabbits is injected into the brains of healthy rabbits, as per the following table:
Rabbit 1 and 2: injected with normal saline on days 1 and 2
The above trials serve as controls.
Rabbit 3 and 4: injected with homogenized brain matter on days 1 and 2
The above trials use unmodified brain matter.
Rabbit 5 and 6: injected with irradiated homogenized brain matter on days 1 and 2
The above trials use brain matter that has been irradiated to destroy nucleic acids in the homogenate.
Rabbit 7 and 8: injected with protein-free centrifuged homogenized brain matter on days 1 and 2
The above trials use brain matter that has been centrifuged to generate a protein-free homogenate and a protein-rich homogenate based on molecular weight.
Rabbit 9 and 10: injected with boiled homogenized brain matter on days 1 and 2
The above trials use brain matter that have been boiled to destroy any bacterial contaminants in the homogenate.
A scientist claims that he has discovered how PrPRes propagates. He claims that the PrPRes interacts with the PrPC by using its own partially negative oxygen atoms to interact with partially positive hydrogen atoms on PrPC. What is true of these bonds?
Tap to reveal answer
Hydrogen bonds are an example of the strongest type of intermolecular bonds. They are, however, still intermolecular, and thus always weaker than covalent bonds.
Hydrogen bonds are an example of the strongest type of intermolecular bonds. They are, however, still intermolecular, and thus always weaker than covalent bonds.
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Cryptosporidium is a genus of gastrointestinal parasite that infects the intestinal epithelium of mammals. Cryptosporidium is water-borne, and is an apicomplexan parasite. This phylum also includes Plasmodium, Babesia, and Toxoplasma.
Apicomplexans are unique due to their apicoplast, an apical organelle that helps penetrate mammalian epithelium. In the case of cryptosporidium, there is an interaction between the surface proteins of mammalian epithelial tissue and those of the apical portion of the cryptosporidium infective stage, or oocyst. A scientist is conducting an experiment to test the hypothesis that the oocyst secretes a peptide compound that neutralizes intestinal defense cells. These defense cells are resident in the intestinal epithelium, and defend the tissue by phagocytizing the oocysts.
She sets up the following experiment:
As the neutralizing compound was believed to be secreted by the oocyst, the scientist collected oocysts onto growth media. The oocysts were grown among intestinal epithelial cells, and then the media was collected. The media was then added to another plate where Toxoplasma gondii was growing with intestinal epithelial cells. A second plate of Toxoplasma gondii was grown with the same type of intestinal epithelium, but no oocyst-sourced media was added.
A scientist is conducting a follow up experiment to the one described above. She is attempting to determine how cryptosporidium adheres to the gastrointestinal mucosa. She determines that the key step is a binding of a surface protein ligand to a receptor. Which of the following forces are common patterns for protein-protein interaction?
I. Hydrogen bonding
II. Coordinate covalent bonding
III. Polar covalent
IV. Metallic bonding
Cryptosporidium is a genus of gastrointestinal parasite that infects the intestinal epithelium of mammals. Cryptosporidium is water-borne, and is an apicomplexan parasite. This phylum also includes Plasmodium, Babesia, and Toxoplasma.
Apicomplexans are unique due to their apicoplast, an apical organelle that helps penetrate mammalian epithelium. In the case of cryptosporidium, there is an interaction between the surface proteins of mammalian epithelial tissue and those of the apical portion of the cryptosporidium infective stage, or oocyst. A scientist is conducting an experiment to test the hypothesis that the oocyst secretes a peptide compound that neutralizes intestinal defense cells. These defense cells are resident in the intestinal epithelium, and defend the tissue by phagocytizing the oocysts.
She sets up the following experiment:
As the neutralizing compound was believed to be secreted by the oocyst, the scientist collected oocysts onto growth media. The oocysts were grown among intestinal epithelial cells, and then the media was collected. The media was then added to another plate where Toxoplasma gondii was growing with intestinal epithelial cells. A second plate of Toxoplasma gondii was grown with the same type of intestinal epithelium, but no oocyst-sourced media was added.
A scientist is conducting a follow up experiment to the one described above. She is attempting to determine how cryptosporidium adheres to the gastrointestinal mucosa. She determines that the key step is a binding of a surface protein ligand to a receptor. Which of the following forces are common patterns for protein-protein interaction?
I. Hydrogen bonding
II. Coordinate covalent bonding
III. Polar covalent
IV. Metallic bonding
Tap to reveal answer
Of the choices listed, only hydrogen bonds would be very common among protein-protein bonds. Covalent bonds are strong and permanent, and so are uncommon between macromolecules. Some proteins form disulfide bridges, or covalent bonds between sulfur atoms intra-molecularly, but inter-molecularly covalent interactions are usually not appropriate.
Of the choices listed, only hydrogen bonds would be very common among protein-protein bonds. Covalent bonds are strong and permanent, and so are uncommon between macromolecules. Some proteins form disulfide bridges, or covalent bonds between sulfur atoms intra-molecularly, but inter-molecularly covalent interactions are usually not appropriate.
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One component of the immune system is the neutrophil, a professional phagocyte that consumes invading cells. The neutrophil is ferried to the site of infection via the blood as pre-neutrophils, or monocytes, ready to differentiate as needed to defend their host.
In order to leave the blood and migrate to the tissues, where infection is active, the monocyte undergoes a process called diapedesis. Diapedesis is a process of extravasation, where the monocyte leaves the circulation by moving in between endothelial cells, enters the tissue, and matures into a neutrophil.
Diapedesis is mediated by a class of proteins called selectins, present on the monocyte membrane and the endothelium. These selectins interact, attract the monocyte to the endothelium, and allow the monocytes to roll along the endothelium until they are able to complete diapedesis by leaving the vasculature and entering the tissues.
The image below shows monocytes moving in the blood vessel, "rolling" along the vessel wall, and eventually leaving the vessel to migrate to the site of infection.
Which of the following is likely true about the interactions between selectins and the "rolling" monocytes?
One component of the immune system is the neutrophil, a professional phagocyte that consumes invading cells. The neutrophil is ferried to the site of infection via the blood as pre-neutrophils, or monocytes, ready to differentiate as needed to defend their host.
In order to leave the blood and migrate to the tissues, where infection is active, the monocyte undergoes a process called diapedesis. Diapedesis is a process of extravasation, where the monocyte leaves the circulation by moving in between endothelial cells, enters the tissue, and matures into a neutrophil.
Diapedesis is mediated by a class of proteins called selectins, present on the monocyte membrane and the endothelium. These selectins interact, attract the monocyte to the endothelium, and allow the monocytes to roll along the endothelium until they are able to complete diapedesis by leaving the vasculature and entering the tissues.
The image below shows monocytes moving in the blood vessel, "rolling" along the vessel wall, and eventually leaving the vessel to migrate to the site of infection.
Which of the following is likely true about the interactions between selectins and the "rolling" monocytes?
Tap to reveal answer
The interactions that give rise to the neutrophil rolling phenomenon are likely the product of intermolecular bonds, such as hydrogen bonds, that often do not require full ionic charges to be present.
Additionally, proteins and carbohydrates are the typical mediators of these interactions, not fatty acids, and they usually form quickly, reversibly, and spontaneously, without the help of local enzymes.
The interactions that give rise to the neutrophil rolling phenomenon are likely the product of intermolecular bonds, such as hydrogen bonds, that often do not require full ionic charges to be present.
Additionally, proteins and carbohydrates are the typical mediators of these interactions, not fatty acids, and they usually form quickly, reversibly, and spontaneously, without the help of local enzymes.
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Type 1 diabetes is a well-understood autoimmune disease. Autoimmune diseases result from an immune system-mediated attack on one’s own body tissues. In normal development, an organ called the thymus introduces immune cells to the body’s normal proteins. This process is called negative selection, as those immune cells that recognize normal proteins are deleted. If cells evade this process, those that recognize normal proteins enter into circulation, where they can attack body tissues. The thymus is also important for activating T-cells that recognize foreign proteins.
As the figure below shows, immune cells typically originate in the bone marrow. Some immune cells, called T-cells, then go to the thymus for negative selection. Those that survive negative selection, enter into general circulation to fight infection. Other cells, called B-cells, directly enter general circulation from the bone marrow. It is a breakdown in this carefully orchestrated process that leads to autoimmune disease, such as type 1 diabetes.
In the process of negative selection described in the passage, the interaction of T-cells and normal body proteins happens via brief and easily broken biochemical bonds. What type of bonding is most probably involved?
Type 1 diabetes is a well-understood autoimmune disease. Autoimmune diseases result from an immune system-mediated attack on one’s own body tissues. In normal development, an organ called the thymus introduces immune cells to the body’s normal proteins. This process is called negative selection, as those immune cells that recognize normal proteins are deleted. If cells evade this process, those that recognize normal proteins enter into circulation, where they can attack body tissues. The thymus is also important for activating T-cells that recognize foreign proteins.
As the figure below shows, immune cells typically originate in the bone marrow. Some immune cells, called T-cells, then go to the thymus for negative selection. Those that survive negative selection, enter into general circulation to fight infection. Other cells, called B-cells, directly enter general circulation from the bone marrow. It is a breakdown in this carefully orchestrated process that leads to autoimmune disease, such as type 1 diabetes.
In the process of negative selection described in the passage, the interaction of T-cells and normal body proteins happens via brief and easily broken biochemical bonds. What type of bonding is most probably involved?
Tap to reveal answer
Hydrogen bonding is characteristic of a great deal of the intermolecular interactions seen in biochemical systems. Ionic and covalent bonding are far too permanent, and T-cells would never escape the thymus were these bonding patterns the principal interactions. Ionic and covalent interactions generally represent intramolecular interactions, while intermolecular interactions are more temporary. Common intermolecular forces are hydrogen bonding, dipole interactions, and van der Waals forces. (Note that hydrogen bonding can also be an intramolecular interaction for certain molecular structures).
Hydrogen bonding is characteristic of a great deal of the intermolecular interactions seen in biochemical systems. Ionic and covalent bonding are far too permanent, and T-cells would never escape the thymus were these bonding patterns the principal interactions. Ionic and covalent interactions generally represent intramolecular interactions, while intermolecular interactions are more temporary. Common intermolecular forces are hydrogen bonding, dipole interactions, and van der Waals forces. (Note that hydrogen bonding can also be an intramolecular interaction for certain molecular structures).
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Which intermolecular force accounts for the fact that alcohols have higher boiling points than alkanes?
Which intermolecular force accounts for the fact that alcohols have higher boiling points than alkanes?
Tap to reveal answer
Hydrogen bonding occurs when the hydrogen atom attached to an electronegative atom of one molecule (in an alcohol, this electronegative atom is oxygen) becomes attracted to an electronegative atom of a different molecule (either oxygen, nitrogen, or fluorine). This attractive force is so strong that it significantly increases the boiling point of the alcohol.
Hydrogen bonding occurs when the hydrogen atom attached to an electronegative atom of one molecule (in an alcohol, this electronegative atom is oxygen) becomes attracted to an electronegative atom of a different molecule (either oxygen, nitrogen, or fluorine). This attractive force is so strong that it significantly increases the boiling point of the alcohol.
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