Unit 6: Molecular motors and mechanobiology - Practice Quiz

BTY269 — Biophysics 60 Questions
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1 Which 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

2 Along 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

3 Along 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

4 In 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

5 In 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

6 Which 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

7 What 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

8 The 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

9 Which 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

10 Molecular 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

11 Microtubules are built from which protein subunit?

Microtubule structure Easy
A. Collagen
B. Tubulin
C. Keratin
D. Actin

12 The 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

13 What 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

14 How many protofilaments typically make up a single microtubule?

Microtubule structure Easy
A. 24
B. 3
C. 7
D. 13

15 Microtubules 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

16 Microtubules are a component of which cellular structure?

Microtubule structure Easy
A. The ribosome
B. The nucleolus
C. The cytoskeleton
D. The cell membrane

17 Mechanobiology 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

18 The 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

19 Which 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

20 Understanding 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

21 A 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

22 During 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

23 Myosin 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

24 Kinesin 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

25 Conventional 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.

26 What 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

27 In 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

28 Melanophores 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

29 Which 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

30 A typical microtubule is composed of how many protofilaments arranged into a hollow cylinder?

Microtubule structure Medium
A. 23
B. 13
C. 4
D. 9

31 Microtubules 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

32 The 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

33 Which 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

34 The 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

35 In animal cells, microtubule minus-ends are typically anchored at the:

Microtubule structure Medium
A. Centrosome (microtubule organizing center)
B. Plasma membrane
C. Nuclear lumen
D. Golgi lumen

36 The 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

37 Mechanotransduction 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

38 Stem 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
A. Muscle cells
B. Bone cells
C. Cartilage cells
D. Neuron-like cells

39 Which 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

40 Endothelial 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

41 Conventional 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

42 A 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.

43 Cytoplasmic 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
A. A rigid neck-linker docking produces uniform 8 nm steps like kinesin
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

44 In 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

45 A 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

46 The 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.

47 Optical-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

48 Microtubules 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

49 A 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

50 Dynamic 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

51 Consider 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.

52 Post-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

53 Taxol (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

54 Cells 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

55 Mesenchymal 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

56 Piezo1 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

57 Tumor 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

58 Endothelial 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

59 In 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

60 The 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