1Which molecule serves as the primary energy source for molecular motors like kinesin and myosin?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Easy
A.Glucose
B.NADH
C.GTP
D.ATP
Correct Answer: ATP
Explanation:
Molecular motors hydrolyze ATP into ADP and inorganic phosphate, and use the released energy to generate mechanical movement.
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2Along which cytoskeletal filament does the motor protein myosin move?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Easy
A.Intermediate filaments
B.Cellulose fibers
C.Microtubules
D.Actin filaments
Correct Answer: Actin filaments
Explanation:
Myosin motors travel along actin filaments, driving processes such as muscle contraction and cargo transport.
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3Along which cytoskeletal track do kinesin and dynein move?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Easy
A.Microtubules
B.Actin filaments
C.Intermediate filaments
D.Collagen fibers
Correct Answer: Microtubules
Explanation:
Both kinesin and dynein are microtubule-based motors that transport cargo along microtubule tracks.
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4In most cells, kinesin generally transports cargo toward which end of the microtubule?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Easy
A.The centrosome
B.The plus end
C.The minus end
D.The lateral surface
Correct Answer: The plus end
Explanation:
Most conventional kinesins move toward the plus end of microtubules, typically directed toward the cell periphery.
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5In which direction along the microtubule does cytoplasmic dynein typically move?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Easy
A.Toward the minus end
B.It does not move directionally
C.Toward the plus end
D.In random directions
Correct Answer: Toward the minus end
Explanation:
Dynein is a minus-end-directed motor, generally carrying cargo toward the cell center where microtubule minus ends are anchored.
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6Which molecular motor is primarily responsible for muscle contraction?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Easy
A.Myosin
B.Kinesin
C.Dynein
D.Tubulin
Correct Answer: Myosin
Explanation:
Myosin interacts with actin filaments to produce the sliding motion that powers muscle contraction.
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7What general term describes the movement of vesicles and organelles within a cell along cytoskeletal tracks?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Easy
A.Endocytosis
B.Intracellular transport
C.Diffusion equilibrium
D.Osmosis
Correct Answer: Intracellular transport
Explanation:
Intracellular transport is the motor-driven movement of cargo such as vesicles and organelles along filaments inside the cell.
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8The part of a motor protein that binds and hydrolyzes ATP is commonly called the:
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Easy
A.Tail domain
B.Lipid tail
C.Motor head domain
D.Membrane anchor
Correct Answer: Motor head domain
Explanation:
The globular head (motor) domain contains the ATP-binding and filament-binding sites that generate movement.
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9Which part of a motor protein such as kinesin usually attaches to the cargo being transported?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Easy
A.The microtubule wall
B.The tail domain
C.The head domain
D.The ATP pocket
Correct Answer: The tail domain
Explanation:
The tail domain of the motor binds cargo, while the head domains interact with the filament to produce motion.
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10Molecular motors are best classified as which type of biological molecule?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Easy
A.Nucleic acids
B.Carbohydrates
C.Lipids
D.Proteins
Correct Answer: Proteins
Explanation:
Kinesin, dynein, and myosin are all proteins that convert chemical energy into mechanical work.
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11Microtubules are built from which protein subunit?
Microtubule structure
Easy
A.Collagen
B.Tubulin
C.Keratin
D.Actin
Correct Answer: Tubulin
Explanation:
Microtubules are polymers of tubulin, assembled from repeating tubulin subunits.
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12The basic building block of a microtubule is a dimer made of which two proteins?
Microtubule structure
Easy
A.-tubulin and actin
B.Actin and myosin
C.Kinesin and dynein
D.-tubulin and -tubulin
Correct Answer: -tubulin and -tubulin
Explanation:
Microtubules are assembled from heterodimers of -tubulin and -tubulin.
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13What is the overall shape of a microtubule?
Microtubule structure
Easy
A.A solid twisted rope
B.A flat sheet
C.A hollow cylindrical tube
D.A branched network
Correct Answer: A hollow cylindrical tube
Explanation:
Microtubules are hollow tubes formed by protofilaments arranged around a central lumen.
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14How many protofilaments typically make up a single microtubule?
Microtubule structure
Easy
A.24
B.3
C.7
D.13
Correct Answer: 13
Explanation:
A typical microtubule is composed of 13 protofilaments arranged side by side to form the wall of the tube.
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15Microtubules are described as polar structures because they have:
Microtubule structure
Easy
A.An electrical charge gradient
B.A magnetic orientation
C.Two identical ends
D.Distinct plus and minus ends
Correct Answer: Distinct plus and minus ends
Explanation:
The two ends of a microtubule differ structurally and dynamically, defined as the plus end and the minus end.
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16Microtubules are a component of which cellular structure?
Microtubule structure
Easy
A.The ribosome
B.The nucleolus
C.The cytoskeleton
D.The cell membrane
Correct Answer: The cytoskeleton
Explanation:
Microtubules, along with actin and intermediate filaments, form part of the cell's cytoskeleton.
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17Mechanobiology mainly studies how cells respond to what kind of signals?
Mechanobiology and its importance in human health
Easy
A.Sound waves
B.Magnetic fields only
C.Radioactive decay
D.Mechanical forces
Correct Answer: Mechanical forces
Explanation:
Mechanobiology examines how cells sense and respond to mechanical forces such as tension, compression, and shear.
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18The process by which cells convert mechanical signals into biochemical responses is called:
Mechanobiology and its importance in human health
Easy
A.Photosynthesis
B.Transcription
C.Mechanotransduction
D.Glycolysis
Correct Answer: Mechanotransduction
Explanation:
Mechanotransduction is the conversion of mechanical stimuli into intracellular biochemical signals.
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19Which structure surrounding cells provides mechanical support and transmits forces in tissues?
Mechanobiology and its importance in human health
Easy
A.The Golgi apparatus
B.The mitochondrion
C.The nuclear envelope
D.The extracellular matrix
Correct Answer: The extracellular matrix
Explanation:
The extracellular matrix provides structural support and transmits mechanical cues that cells sense and respond to.
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20Understanding mechanobiology is important in human health because abnormal mechanical signaling can contribute to:
Mechanobiology and its importance in human health
Easy
A.Faster nerve conduction only
B.Improved immunity always
C.Diseases such as cancer
D.Reduced cell size only
Correct Answer: Diseases such as cancer
Explanation:
Disrupted mechanical signaling is linked to conditions like cancer, fibrosis, and cardiovascular disease, making mechanobiology medically important.
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21A vesicle needs to be transported from the cell center toward the plus-end of a microtubule near the cell periphery. Which motor protein is most likely responsible for this movement?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Medium
A.Cytoplasmic dynein
B.Dynactin alone
C.Myosin II
D.Conventional kinesin, which walks processively toward the plus-end of microtubules using ATP hydrolysis to power vesicle transport toward the periphery
Correct Answer: Conventional kinesin, which walks processively toward the plus-end of microtubules using ATP hydrolysis to power vesicle transport toward the periphery
Explanation:
Kinesin is a plus-end-directed motor, moving cargo toward microtubule plus-ends typically located at the cell periphery. Dynein moves toward the minus-end (cell center).
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22During retrograde axonal transport, damaged organelles move from the axon terminal back toward the cell body. Which motor drives this movement?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Medium
A.Kinesin-1
B.Cytoplasmic dynein
C.Myosin VI
D.Myosin V
Correct Answer: Cytoplasmic dynein
Explanation:
Retrograde transport (toward the cell body) occurs along microtubule minus-ends, which is powered by cytoplasmic dynein.
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23Myosin motors primarily move along which cytoskeletal filament?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Medium
A.Microtubules
B.Intermediate filaments
C.Septins
D.Actin filaments
Correct Answer: Actin filaments
Explanation:
Myosins are actin-based motors, whereas kinesins and dyneins move along microtubules.
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24Kinesin is described as a 'processive' motor. What does processivity mean in this context?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Medium
A.The motor hydrolyzes GTP instead of ATP
B.The motor works only in muscle tissue
C.The motor takes many consecutive steps along a filament before detaching
D.The motor moves only in the minus-end direction
Correct Answer: The motor takes many consecutive steps along a filament before detaching
Explanation:
Processivity refers to a motor's ability to take multiple steps along its track without dissociating, allowing sustained cargo transport.
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25Conventional kinesin moves along a microtubule using a 'hand-over-hand' mechanism with an approximate step size of:
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Medium
A.
B.
C.
D.
Correct Answer:
Explanation:
Kinesin takes steps, matching the periodicity of the tubulin dimer along the microtubule protofilament.
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26What is the primary energy source that powers the walking motion of kinesin and dynein motors?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Medium
A.Hydrolysis of GTP
B.NADH oxidation
C.Hydrolysis of ATP
D.Proton gradient across the membrane
Correct Answer: Hydrolysis of ATP
Explanation:
Both kinesin and dynein are ATPases; the chemical energy from ATP hydrolysis is converted into mechanical stepping motion.
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27In muscle contraction, the sliding filament model relies on which myosin activity?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Medium
A.Myosin nucleating new microtubules
B.Myosin heads binding actin and undergoing a power stroke, pulling actin filaments toward the sarcomere center while cyclically hydrolyzing ATP
C.Myosin transporting mitochondria along microtubules
D.Myosin depolymerizing actin filaments
Correct Answer: Myosin heads binding actin and undergoing a power stroke, pulling actin filaments toward the sarcomere center while cyclically hydrolyzing ATP
Explanation:
Muscle myosin (myosin II) cross-bridges bind actin and perform a power stroke, sliding thin filaments inward to shorten the sarcomere.
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28Melanophores can rapidly aggregate or disperse pigment granules. Dispersion toward the cell periphery is mainly driven by:
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Medium
A.Cytoplasmic dynein
B.Tubulin polymerization alone
C.Kinesin
D.Myosin II
Correct Answer: Kinesin
Explanation:
Dispersion of pigment granules toward the periphery uses plus-end-directed kinesin, while aggregation toward the center uses minus-end-directed dynein.
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29Which structural feature of kinesin allows two heads to coordinate their ATPase cycles for processive walking?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Medium
A.A long coiled-coil tail only
B.A calcium-binding light chain
C.A single globular head
D.A neck linker connecting the motor domains
Correct Answer: A neck linker connecting the motor domains
Explanation:
The neck linker mechanically couples the two motor heads, allowing alternating ATPase cycles that produce coordinated hand-over-hand stepping.
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30A typical microtubule is composed of how many protofilaments arranged into a hollow cylinder?
Microtubule structure
Medium
A.23
B.13
C.4
D.9
Correct Answer: 13
Explanation:
Most cellular microtubules contain 13 protofilaments of tubulin dimers forming a hollow tube about in diameter.
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31Microtubules are polar structures. This polarity arises because:
Microtubule structure
Medium
A.Alpha-tubulin carries a net positive charge
B.The lumen is positively charged and the surface negatively charged
C.Tubulin dimers assemble head-to-tail, giving distinct plus and minus ends with different subunits exposed
D.GTP caps make one end acidic
Correct Answer: Tubulin dimers assemble head-to-tail, giving distinct plus and minus ends with different subunits exposed
Explanation:
-tubulin dimers polymerize head-to-tail, so the two ends differ structurally, defining the fast-growing plus end and slow-growing minus end.
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32The dynamic behavior in which individual microtubules switch between growth and rapid shrinkage is called:
Microtubule structure
Medium
A.Dynamic instability
B.Cooperative binding
C.Isodesmic assembly
D.Treadmilling
Correct Answer: Dynamic instability
Explanation:
Dynamic instability describes stochastic switching between polymerization (rescue) and depolymerization (catastrophe), governed by the GTP cap.
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33Which nucleotide state of tubulin at the microtubule end promotes stability and continued growth?
Microtubule structure
Medium
A.A GDP-bound cap
B.An ATP-bound cap
C.A GTP-bound cap
D.An AMP-bound cap
Correct Answer: A GTP-bound cap
Explanation:
A GTP cap at the plus end stabilizes the lattice and favors growth; loss of the cap (GDP-tubulin exposed) triggers catastrophe.
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34The building block of microtubules is a heterodimer consisting of:
Microtubule structure
Medium
A.One -tubulin and one -tubulin
B.-tubulin and -tubulin
C.Actin and tubulin
D.Two identical -tubulin monomers
Correct Answer: One -tubulin and one -tubulin
Explanation:
The fundamental subunit is the -tubulin heterodimer, which polymerizes to form protofilaments.
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35In animal cells, microtubule minus-ends are typically anchored at the:
The centrosome serves as the main MTOC, nucleating microtubules with their minus-ends anchored there and plus-ends extending outward.
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36The anti-cancer drug Taxol (paclitaxel) affects microtubules by:
Microtubule structure
Medium
A.Depolymerizing all actin filaments
B.Stabilizing microtubules and preventing depolymerization, thereby blocking mitotic spindle dynamics and arresting dividing cells in mitosis
C.Blocking ATP binding to kinesin
D.Preventing tubulin gene transcription
Correct Answer: Stabilizing microtubules and preventing depolymerization, thereby blocking mitotic spindle dynamics and arresting dividing cells in mitosis
Explanation:
Taxol binds -tubulin and stabilizes microtubules, suppressing the dynamics needed for spindle function and thus arresting cell division.
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37Mechanotransduction refers to the process by which cells:
Mechanobiology and its importance in human health
Medium
A.Convert mechanical stimuli into biochemical signals
B.Convert light into electrical signals
C.Replicate DNA in response to stretch
D.Synthesize ATP from mechanical strain only
Correct Answer: Convert mechanical stimuli into biochemical signals
Explanation:
Mechanotransduction is the conversion of mechanical forces (stretch, shear, stiffness) into biochemical and gene-expression responses inside the cell.
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38Stem cells cultured on substrates of different stiffness can differentiate along distinct lineages. Cells grown on a soft, brain-like matrix tend to become:
Mechanobiology and its importance in human health
Medium
39Which cell-surface structures physically link the extracellular matrix to the intracellular cytoskeleton and sense mechanical force?
Mechanobiology and its importance in human health
Medium
A.Peroxisomes
B.Nuclear pores
C.Integrins at focal adhesions
D.Gap junctions
Correct Answer: Integrins at focal adhesions
Explanation:
Integrins bind ECM proteins externally and connect to actin via focal adhesion complexes, serving as key mechanosensors.
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40Endothelial cells lining blood vessels sense blood flow. The relevant mechanical stimulus they primarily detect is:
Mechanobiology and its importance in human health
Medium
A.Thermal gradients
B.Fluid shear stress
C.Osmotic pressure
D.Magnetic flux
Correct Answer: Fluid shear stress
Explanation:
Flowing blood exerts shear stress on the endothelial surface; abnormal shear patterns are linked to atherosclerosis and vascular disease.
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41Conventional kinesin-1 moves processively along microtubules by a hand-over-hand mechanism. If one head detaches before the trailing head has completed its ATP-dependent power stroke, the motor risks dissociation. Which coordination feature most directly prevents both heads from releasing simultaneously?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Hard
A.Simultaneous ATP hydrolysis in both heads triggered by microtubule binding
B.A high for ATP that slows the catalytic cycle uniformly
C.Intramolecular strain (internal tension) that gates the nucleotide state of the two heads
D.Random independent stepping that statistically keeps one head bound
Correct Answer: Intramolecular strain (internal tension) that gates the nucleotide state of the two heads
Explanation:
Mechanical strain communicated through the neck linker couples the two heads out of phase: tension inhibits ATP binding in the leading head until the trailing head steps, ensuring at least one head stays bound. This gating gives kinesin its high processivity.
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42A kinesin motor takes discrete 8 nm steps and hydrolyzes one ATP per step. If a single motor sustains an average velocity of under low load, what is its approximate ATP turnover (stepping) rate?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Hard
A.
B.
C.
D.
Correct Answer:
Explanation:
Rate steps/s. With one ATP per step, the turnover is .
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43Cytoplasmic dynein differs fundamentally from kinesin in its stepping behavior. Which observation best reflects dynein's structural mechanism of force generation?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Hard
B.Force is generated by lever-arm swing of a myosin-like converter domain
C.A conformational change in the AAA+ ring and linker drives movement, producing variable step sizes
D.Movement is powered by GTP hydrolysis rather than ATP
Correct Answer: A conformational change in the AAA+ ring and linker drives movement, producing variable step sizes
Explanation:
Dynein is an AAA+ ATPase; ATP hydrolysis in AAA1 drives a linker-domain swing across the ring that shifts the microtubule-binding stalk. This gives dynein its characteristic variable step sizes (8–32 nm), unlike kinesin's uniform steps.
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44In an in vitro motility assay, myosin V walks processively along actin with 36 nm steps, while myosin II is non-processive. What structural feature primarily accounts for myosin V's processivity relative to myosin II?
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Hard
A.The absence of an ATPase head allowing continuous binding
B.A long lever arm with 6 IQ/light-chain motifs and high duty ratio
C.A higher intrinsic sliding velocity of the actin filament
D.A shorter lever arm that speeds detachment from actin
Correct Answer: A long lever arm with 6 IQ/light-chain motifs and high duty ratio
Explanation:
Myosin V has a long neck (6 calmodulin/light chains) matching actin's 36 nm helical repeat and a high duty ratio (spends most of its cycle bound). This keeps at least one head attached, enabling processive movement, unlike low-duty-ratio myosin II.
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45A neuron transports cargo bidirectionally along an axon. Anterograde and retrograde vesicle movements often reverse rapidly on the same track. The most widely supported explanation for this bidirectional switching is:
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Hard
A.Alternating ATP and GTP fueling of a single motor type
B.Rapid rebuilding of microtubules with reversed polarity between movements
C.A tug-of-war between oppositely directed kinesin and dynein motors bound to the same cargo
D.Kinesin reversing its own directionality upon reaching high load
Correct Answer: A tug-of-war between oppositely directed kinesin and dynein motors bound to the same cargo
Explanation:
Cargos typically carry both plus-end (kinesin) and minus-end (dynein) motors. The net direction reflects the balance of forces (and regulation) in a tug-of-war; shifting the balance produces rapid reversals without altering the track.
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46The stall force of a single kinesin-1 is about over an step. Comparing the mechanical work per step to the free energy of ATP hydrolysis ( under cellular conditions), the approximate thermodynamic efficiency is:
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Hard
A.
B.
C.
D.
Correct Answer:
Explanation:
Work per step . Efficiency , i.e. about 60%, reflecting kinesin's high mechanochemical efficiency near stall.
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47Optical-trap experiments show that when kinesin's neck linker is artificially lengthened, processivity and velocity both drop sharply. This is best explained because a longer neck linker:
Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement
Hard
A.Prevents the motor from binding the microtubule altogether
B.Reverses the directionality of stepping toward the minus end
C.Increases the ATP hydrolysis rate beyond the mechanical cycle
D.Weakens the internal strain that coordinates the two heads' catalytic cycles
Correct Answer: Weakens the internal strain that coordinates the two heads' catalytic cycles
Explanation:
The short neck linker transmits tension between heads to gate nucleotide binding. Lengthening it dissipates this strain, decoupling the heads so they can both release, reducing processivity and velocity.
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48Microtubules are built from -tubulin heterodimers arranged into protofilaments. The structural basis for microtubule polarity, essential for directed motor transport, is that:
Microtubule structure
Hard
A.Heterodimers align head-to-tail so -tubulin is exposed at the plus end and -tubulin at the minus end
B.Protofilaments alternate and subunits laterally to form a symmetric wall
C.Polarity arises from GTP bound only to the -tubulin subunit
D.The plus end is capped by -tubulin and grows more slowly than the minus end
Correct Answer: Heterodimers align head-to-tail so -tubulin is exposed at the plus end and -tubulin at the minus end
Explanation:
Head-to-tail (α→β) polymerization of dimers within each protofilament gives the microtubule structural polarity: the fast-growing plus end exposes β-tubulin, the minus end exposes α-tubulin. This polarity directs kinesin (plus) and dynein (minus) transport.
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49A typical microtubule has 13 protofilaments arranged with a slight lateral stagger, creating a helical 'seam.' The functional significance of the 13-protofilament, B-lattice arrangement is that it:
Microtubule structure
Hard
A.Maximizes the microtubule diameter for maximal cargo capacity
B.Eliminates the GTP cap required for dynamic instability
C.Forces protofilaments into a strongly left-handed supercoil
D.Allows protofilaments to run nearly parallel to the microtubule axis, providing a straight track for motors
Correct Answer: Allows protofilaments to run nearly parallel to the microtubule axis, providing a straight track for motors
Explanation:
The 13-protofilament architecture (with a single seam) keeps protofilaments essentially parallel to the long axis, so motors follow a straight path rather than spiraling. Non-13 lattices cause supertwist and skewed motor tracking.
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50Dynamic instability of microtubules is governed by the nucleotide state of -tubulin. The transition from growth to rapid shrinkage (catastrophe) occurs when:
Microtubule structure
Hard
A.Lateral bonds strengthen as GDP-tubulin accumulates
B.The stabilizing GTP cap is lost, exposing GDP-tubulin that favors protofilament peeling
C.Free tubulin concentration rises above the critical concentration
D.GTP hydrolysis on -tubulin releases the lateral bonds
Correct Answer: The stabilizing GTP cap is lost, exposing GDP-tubulin that favors protofilament peeling
Explanation:
GTP-tubulin at the growing tip forms a stabilizing cap. When hydrolysis outpaces addition and the cap is lost, strained GDP-tubulin protofilaments curl outward and depolymerize rapidly — catastrophe.
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51Consider a microtubule with 13 protofilaments and a tubulin dimer length of . If the microtubule elongates by adding 260 dimers total distributed evenly, by how much does its length increase?
Microtubule structure
Hard
A.
B.
C.
D.
Correct Answer:
Explanation:
Dimers distribute across 13 protofilaments: dimers per protofilament. Length gain , since length grows along protofilaments, not by total dimer count.
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52Post-translational modifications (PTMs) such as detyrosination, acetylation, and polyglutamylation form the 'tubulin code.' A key functional consequence relevant to intracellular transport is that PTMs:
Microtubule structure
Hard
A.Modulate the recruitment and processivity of specific motors and MAPs on microtubule subsets
B.Provide the chemical energy for motor stepping
C.Convert -tubulin into -tubulin over time
D.Directly change the number of protofilaments in the lattice
Correct Answer: Modulate the recruitment and processivity of specific motors and MAPs on microtubule subsets
Explanation:
The tubulin code marks distinct microtubule populations; PTMs alter binding affinity and processivity of motors (e.g., kinesins) and MAPs, effectively routing cargo to specific tracks. They do not provide energy or change subunit identity.
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53Taxol (paclitaxel) is a chemotherapeutic that binds -tubulin. Its anti-mitotic effect arises because taxol:
Microtubule structure
Hard
A.Depolymerizes microtubules by stripping the GTP cap
B.Severs microtubules into short non-functional fragments
C.Stabilizes microtubules and suppresses dynamic instability, blocking mitotic spindle function
D.Sequesters free tubulin dimers to prevent any polymerization
Correct Answer: Stabilizes microtubules and suppresses dynamic instability, blocking mitotic spindle function
Explanation:
Taxol binds and hyperstabilizes microtubules, suppressing the dynamic instability required for spindle chromosome capture and segregation. Cells arrest in mitosis. (Colchicine/vinblastine, by contrast, inhibit polymerization.)
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54Cells sense the stiffness of their extracellular matrix (ECM) and translate it into biochemical signals — a process called mechanotransduction. Which molecular event is central to converting matrix stiffness into altered gene expression?
Mechanobiology and its importance in human health
Hard
A.Voltage-gated calcium channels responding only to membrane potential
B.Diffusion of ECM proteins into the nucleus to bind DNA directly
C.Passive osmotic swelling that ruptures the nuclear envelope
D.Force-dependent unfolding of talin/exposure of cryptic sites reinforcing focal adhesions and activating YAP/TAZ signaling
Correct Answer: Force-dependent unfolding of talin/exposure of cryptic sites reinforcing focal adhesions and activating YAP/TAZ signaling
Explanation:
On stiff matrices, tension unfolds talin and exposes cryptic binding sites (e.g., for vinculin), reinforcing focal adhesions and the actin cytoskeleton. This drives nuclear translocation of YAP/TAZ, altering gene expression — a core mechanotransduction pathway.
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55Mesenchymal stem cells cultured on substrates of differing stiffness differentiate along distinct lineages. On a stiff, bone-like matrix (–), the predominant outcome is:
Mechanobiology and its importance in human health
Hard
A.Complete loss of differentiation potential regardless of stiffness
B.Neurogenic differentiation favored by minimal contractility
C.Adipogenic differentiation due to low actomyosin tension
D.Osteogenic differentiation driven by high cytoskeletal tension and YAP activation
Correct Answer: Osteogenic differentiation driven by high cytoskeletal tension and YAP activation
Explanation:
Engler et al. showed stiff (bone-mimicking) substrates promote osteogenesis via high cytoskeletal tension and nuclear YAP; soft (brain-like) matrices favor neurogenesis, and intermediate (muscle-like) favor myogenesis. Matrix elasticity directs lineage.
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56Piezo1 is a mechanically gated ion channel important in vascular and epithelial physiology. Its gating mechanism is best described as:
Mechanobiology and its importance in human health
Hard
A.Ligand binding at an extracellular pocket that triggers channel opening
B.Phosphorylation of its C-terminus by a mechanosensitive kinase
C.Membrane tension flattening its curved, blade-like domains to open the pore
D.ATP hydrolysis within the channel driving conformational opening
Correct Answer: Membrane tension flattening its curved, blade-like domains to open the pore
Explanation:
Piezo1 has a trimeric propeller/blade structure that curves the local membrane. Increased membrane tension flattens these blades, opening the central pore to cation flux — an intrinsically force-gated (not ligand- or ATP-driven) mechanism.
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57Tumor progression is associated with ECM stiffening. Increased matrix stiffness promotes malignancy primarily by:
Mechanobiology and its importance in human health
Hard
A.Reducing intracellular tension so cells become quiescent
B.Enhancing integrin clustering and mechanosignaling that boost proliferation, survival, and invasion
C.Physically blocking all cell migration through the tissue
D.Preventing angiogenesis and thereby starving the tumor
Correct Answer: Enhancing integrin clustering and mechanosignaling that boost proliferation, survival, and invasion
Explanation:
A stiffer ECM increases integrin clustering, focal-adhesion signaling, and Rho/ROCK-driven contractility, activating growth and survival pathways (e.g., ERK, YAP) and promoting invasive behavior. Stiffening is a driver, not a brake, of malignancy.
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58Endothelial cells lining blood vessels respond to laminar shear stress from blood flow. Physiological laminar shear is generally atheroprotective because it:
Mechanobiology and its importance in human health
Hard
A.Blocks nitric oxide production and raises vascular tone
B.Causes endothelial cells to detach from the basement membrane
C.Aligns cells with flow and promotes anti-inflammatory, vasodilatory signaling (e.g., eNOS/NO)
D.Triggers sustained NF-B inflammation and endothelial disarray
Correct Answer: Aligns cells with flow and promotes anti-inflammatory, vasodilatory signaling (e.g., eNOS/NO)
Explanation:
Steady laminar shear elongates and aligns endothelial cells with flow and upregulates eNOS/NO and anti-inflammatory programs. Disturbed/oscillatory flow at vessel branches instead promotes inflammation and atherosclerosis.
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59In muscular dystrophies, mutations in the dystrophin–glycoprotein complex cause fiber damage. From a mechanobiology standpoint, the core defect is that:
Mechanobiology and its importance in human health
Hard
A.Actin and myosin filaments are chemically unable to interact
B.Muscle cells can no longer produce ATP for contraction
C.Motor neurons fail to release acetylcholine at the synapse
D.Loss of mechanical linkage between the cytoskeleton and ECM makes the membrane fragile under contractile force
Correct Answer: Loss of mechanical linkage between the cytoskeleton and ECM makes the membrane fragile under contractile force
Explanation:
Dystrophin mechanically couples the internal actin cytoskeleton to the ECM via the glycoprotein complex, distributing contractile stress. Without it, the sarcolemma tears during repeated contraction, causing progressive fiber damage.
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60The LINC complex (SUN and nesprin proteins) spans the nuclear envelope. Its role in mechanobiology is to:
Mechanobiology and its importance in human health
Hard
A.Serve solely as a passive diffusion barrier for ions
B.Physically couple the cytoskeleton to the nuclear lamina, transmitting force to reshape chromatin and nuclear signaling
C.Depolymerize microtubules that contact the nucleus
D.Generate ATP-driven force for chromosome movement during mitosis
Correct Answer: Physically couple the cytoskeleton to the nuclear lamina, transmitting force to reshape chromatin and nuclear signaling
Explanation:
LINC complexes bridge nesprins (outer membrane, cytoskeleton-binding) and SUN proteins (inner membrane, lamina-binding), providing a continuous mechanical path from ECM to nucleus. Force through LINC deforms the nucleus and modulates chromatin/gene expression.
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