Exam 17: Cytoskeleton

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Which of the following items is not important for flagellar movement?

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The graph in Figure 17-10 shows the time course of the polymerization of pure tubulin in vitro.You can assume that the starting concentration of free tubulin is much higher than it is in cells. The graph in Figure 17-10 shows the time course of the polymerization of pure tubulin in vitro.You can assume that the starting concentration of free tubulin is much higher than it is in cells.    Figure 17-10 A.Explain the reason for the initial lag in the rate of microtubule formation. B.Why does the curve level out after point C? Figure 17-10 A.Explain the reason for the initial lag in the rate of microtubule formation. B.Why does the curve level out after point C?

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The graph in Figure 17-18 shows the time course of the polymerization of pure tubulin in vitro.Assume that the starting concentration of free tubulin is higher than it is in cells. The graph in Figure 17-18 shows the time course of the polymerization of pure tubulin in vitro.Assume that the starting concentration of free tubulin is higher than it is in cells.   Figure 17-18 Three parts of the curve are labeled above it as A, B, and C.You conduct a similar in vitro tubulin-polymerization experiment, only this time you include purified centrosomes in your preparation.When you plot your data, which part of your graph should be most dissimilar to the curve shown in Figure 17-18? Figure 17-18 Three parts of the curve are labeled above it as A, B, and C.You conduct a similar in vitro tubulin-polymerization experiment, only this time you include purified centrosomes in your preparation.When you plot your data, which part of your graph should be most dissimilar to the curve shown in Figure 17-18?

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Indicate whether each of the following statements refers to a ciliary microtubule, a microtubule of the mitotic spindle, both types of microtubule, or neither type of microtubule. A.The basal body is the organizing center. B.The monomer is sequestered by profilin. C.It is arranged in a "9 + 2" array. D.It is nucleated at the centrosome. E.It uses dynein motors. F.It is involved in sperm motility. G.It is involved in moving fluid over the surface of cells.

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Phosphorylation of nuclear lamins regulates their assembly and disassembly during mitosis.You add a drug to cells undergoing mitosis that inhibits the activity of an enzyme that dephosphorylates nuclear lamins.What do you predict will happen to these cells? Why?

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Which of the following statements about the movement of materials in a nerve axon is TRUE?

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Which of the following statements about the cytoskeleton is TRUE?

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Which of the following statements about the cytoskeleton is FALSE?

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Compared to the normal situation, in which actin monomers carry ATP, what do you predict would happen if actin monomers that bind a nonhydrolyzable form of ATP were incorporated into actin filaments?

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Cell movement involves the coordination of many events in the cell.Which of the following phenomena is not required for cell motility?

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Which of the following statements about skeletal muscle contraction is FALSE?

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You are examining a cell line in which activation of the Rho family member Rac promotes lamellipodia formation.Which of the following statements is most likely to be TRUE?

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Your friend discovers a protein that she names EBP.EBP binds to microtubule plus ends, and she hypothesizes a role for EBP in increasing dynamic instability.To determine the function of EBP, she examines its effect on microtubules.She polymerizes microtubules from purified centrosomes in a Petri plate and determines the number of shrinking microtubules over a three-minute time interval for different concentrations of EBP.The data she obtained are shown in Figure 17-8. (A) Your friend discovers a protein that she names EBP.EBP binds to microtubule plus ends, and she hypothesizes a role for EBP in increasing dynamic instability.To determine the function of EBP, she examines its effect on microtubules.She polymerizes microtubules from purified centrosomes in a Petri plate and determines the number of shrinking microtubules over a three-minute time interval for different concentrations of EBP.The data she obtained are shown in Figure 17-8. (A)    (B)    (C)      Figure 17-8 Is this result consistent with her hypothesis? Explain. (B) Your friend discovers a protein that she names EBP.EBP binds to microtubule plus ends, and she hypothesizes a role for EBP in increasing dynamic instability.To determine the function of EBP, she examines its effect on microtubules.She polymerizes microtubules from purified centrosomes in a Petri plate and determines the number of shrinking microtubules over a three-minute time interval for different concentrations of EBP.The data she obtained are shown in Figure 17-8. (A)    (B)    (C)      Figure 17-8 Is this result consistent with her hypothesis? Explain. (C) Your friend discovers a protein that she names EBP.EBP binds to microtubule plus ends, and she hypothesizes a role for EBP in increasing dynamic instability.To determine the function of EBP, she examines its effect on microtubules.She polymerizes microtubules from purified centrosomes in a Petri plate and determines the number of shrinking microtubules over a three-minute time interval for different concentrations of EBP.The data she obtained are shown in Figure 17-8. (A)    (B)    (C)      Figure 17-8 Is this result consistent with her hypothesis? Explain. Figure 17-8 Is this result consistent with her hypothesis? Explain.

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You are curious about the dynamic instability of microtubules and decide to join a lab that works on microtubule polymerization.The people in the lab help you grow some microtubules in culture using conditions that allow you to watch individual microtubules under a microscope.You can see the microtubules growing and shrinking, as you expect.The professor who runs the lab gets in a new piece of equipment, a very fine laser beam that can be used to sever microtubules.She is very excited and wants to sever growing microtubules at their middle, using the laser beam. A.Do you predict that the newly exposed microtubule plus ends will grow or shrink? Explain your answer. B.What do you expect would happen to the newly exposed plus ends if you were to grow the microtubules in the presence of an analog of GTP that cannot be hydrolyzed, and you then severed the microtubules in the middle with a laser beam?

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Do you agree or disagree with this statement? Explain your answer. Minus-end directed microtubule motors (like dyneins) deliver their cargo to the periphery of the cell, whereas plus-end directed microtubule motors (like kinesins) deliver their cargo to the interior of the cell.

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Figure 17-21 shows two isolated outer-doublet microtubules from a eukaryotic flagellum with their associated dynein molecules. Figure 17-21 shows two isolated outer-doublet microtubules from a eukaryotic flagellum with their associated dynein molecules.    Figure 17-21 A.Sketch what will happen to this structure if it is supplied with ATP. B.Sketch what will happen to this structure if the linking proteins are removed and it is supplied with ATP. C.In a complete flagellum, what would happen if all the dynein molecules were active at the same time? Figure 17-21 A.Sketch what will happen to this structure if it is supplied with ATP. B.Sketch what will happen to this structure if the linking proteins are removed and it is supplied with ATP. C.In a complete flagellum, what would happen if all the dynein molecules were active at the same time?

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For each of the following sentences, fill in the blanks with the best word or phrase selected from the list below.Not all words or phrases will be used; use each word or phrase only once. antiparallel four tail \beta barrel globular ten coiled-coil head trimeric covalent rod twenty-five eight seven two Intermediate filaments are elongated fibrous proteins with an N-terminal globular __________ region and a C-terminal globular __________ region; these regions flank the elongated rod domain.The α-helical region of the rod interacts with the α-helical region of another monomer in a __________ configuration to form a dimer.__________ dimers will line up to form a staggered tetramer.__________ strands of tetramers come together and twist together to form the __________ nm filament.The __________ domains are exposed on the surface of the intermediate filament, allowing for interaction with cytoplasmic components.

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You discover a protein, MtA, and find that it binds to the plus ends of microtubules in cells.The hypothesis that best explains this localization is that MtA

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Kinesins were purified by adding the nonhydrolyzable analog AMP-PNP to cytoplasmic extracts containing microtubules, purifying the microtubules, and then releasing the kinesin proteins, which were still attached to the microtubules, by adding ATP.Would this trick have worked to purify myosin motors attached to actin filaments? Explain.

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Which of the statements below about intermediate filaments is FALSE?

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