Unit 6: Molecular motors and mechanobiology - Practice Quiz

BTY269 — Biophysics 60 Questions
0 Correct 0 Wrong 60 Left
0/60

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. NADH
B. Glucose
C. ATP
D. GTP

2 Along which cytoskeletal filament does the motor protein myosin move?

Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement Easy
A. Cellulose fibers
B. Intermediate filaments
C. Actin filaments
D. Microtubules

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 minus end
B. The centrosome
C. The lateral surface
D. The plus end

5 In which direction along the microtubule does cytoplasmic dynein typically move?

Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement Easy
A. It does not move directionally
B. Toward the plus end
C. In random directions
D. Toward the minus end

6 Which molecular motor is primarily responsible for muscle contraction?

Molecular Motors: Kinesin, Dynein and Myosin, and intracellular movement Easy
A. Tubulin
B. Myosin
C. Kinesin
D. Dynein

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. Osmosis
B. Diffusion equilibrium
C. Endocytosis
D. Intracellular transport

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. Motor head domain
B. Tail domain
C. Membrane anchor
D. Lipid tail

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 tail domain
B. The microtubule wall
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. Proteins
C. Carbohydrates
D. Lipids

11 Microtubules are built from which protein subunit?

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

12 The basic building block of a microtubule is a dimer made of which two proteins?

Microtubule structure Easy
A. Actin and myosin
B. -tubulin and -tubulin
C. Kinesin and dynein
D. -tubulin and actin

13 What is the overall shape of a microtubule?

Microtubule structure Easy
A. A hollow cylindrical tube
B. A branched network
C. A flat sheet
D. A solid twisted rope

14 How many protofilaments typically make up a single microtubule?

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

15 Microtubules are described as polar structures because they have:

Microtubule structure Easy
A. Two identical ends
B. An electrical charge gradient
C. Distinct plus and minus ends
D. A magnetic orientation

16 Microtubules are a component of which cellular structure?

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

17 Mechanobiology mainly studies how cells respond to what kind of signals?

Mechanobiology and its importance in human health Easy
A. Sound waves
B. Mechanical forces
C. Radioactive decay
D. Magnetic fields only

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 nuclear envelope
B. The mitochondrion
C. The extracellular matrix
D. The Golgi apparatus

20 Understanding mechanobiology is important in human health because abnormal mechanical signaling can contribute to:

Mechanobiology and its importance in human health Easy
A. Diseases such as cancer
B. Reduced cell size only
C. Improved immunity always
D. Faster nerve conduction 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. Conventional kinesin, which walks processively toward the plus-end of microtubules using ATP hydrolysis to power vesicle transport toward the periphery
B. Dynactin alone
C. Cytoplasmic dynein
D. Myosin II

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. Cytoplasmic dynein
B. Kinesin-1
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. Septins
B. Microtubules
C. Intermediate filaments
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 works only in muscle tissue
B. The motor hydrolyzes GTP instead of ATP
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. Proton gradient across the membrane
B. NADH oxidation
C. Hydrolysis of ATP
D. Hydrolysis of GTP

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 heads binding actin and undergoing a power stroke, pulling actin filaments toward the sarcomere center while cyclically hydrolyzing ATP
B. Myosin nucleating new microtubules
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. Myosin II
B. Cytoplasmic dynein
C. Kinesin
D. Tubulin polymerization alone

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 single globular head
B. A calcium-binding light chain
C. A long coiled-coil tail only
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. 4
B. 13
C. 23
D. 9

31 Microtubules are polar structures. This polarity arises because:

Microtubule structure Medium
A. Alpha-tubulin carries a net positive charge
B. GTP caps make one end acidic
C. Tubulin dimers assemble head-to-tail, giving distinct plus and minus ends with different subunits exposed
D. The lumen is positively charged and the surface negatively charged

32 The dynamic behavior in which individual microtubules switch between growth and rapid shrinkage is called:

Microtubule structure Medium
A. Isodesmic assembly
B. Cooperative binding
C. Dynamic instability
D. Treadmilling

33 Which nucleotide state of tubulin at the microtubule end promotes stability and continued growth?

Microtubule structure Medium
A. A GTP-bound cap
B. An ATP-bound cap
C. An AMP-bound cap
D. A GDP-bound cap

34 The building block of microtubules is a heterodimer consisting of:

Microtubule structure Medium
A. Two identical -tubulin monomers
B. Actin and tubulin
C. -tubulin and -tubulin
D. One -tubulin and one -tubulin

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

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

36 The anti-cancer drug Taxol (paclitaxel) affects microtubules by:

Microtubule structure Medium
A. Stabilizing microtubules and preventing depolymerization, thereby blocking mitotic spindle dynamics and arresting dividing cells in mitosis
B. Depolymerizing all actin filaments
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 light into electrical signals
B. Replicate DNA in response to stretch
C. Convert mechanical stimuli into biochemical signals
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. Bone cells
B. Muscle cells
C. Neuron-like cells
D. Cartilage 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. Gap junctions
B. Integrins at focal adhesions
C. Nuclear pores
D. Peroxisomes

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. Fluid shear stress
B. Magnetic flux
C. Thermal gradients
D. Osmotic pressure

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. Intramolecular strain (internal tension) that gates the nucleotide state of the two heads
B. Simultaneous ATP hydrolysis in both heads triggered by microtubule binding
C. A high for ATP that slows the catalytic cycle uniformly
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 conformational change in the AAA+ ring and linker drives movement, producing variable step sizes
B. A rigid neck-linker docking produces uniform 8 nm steps like kinesin
C. Movement is powered by GTP hydrolysis rather than ATP
D. Force is generated by lever-arm swing of a myosin-like converter domain

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. A higher intrinsic sliding velocity of the actin filament
B. A long lever arm with 6 IQ/light-chain motifs and high duty ratio
C. A shorter lever arm that speeds detachment from actin
D. The absence of an ATPase head allowing continuous binding

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. A tug-of-war between oppositely directed kinesin and dynein motors bound to the same cargo
B. Alternating ATP and GTP fueling of a single motor type
C. Rapid rebuilding of microtubules with reversed polarity between movements
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. Increases the ATP hydrolysis rate beyond the mechanical cycle
B. Weakens the internal strain that coordinates the two heads' catalytic cycles
C. Reverses the directionality of stepping toward the minus end
D. Prevents the motor from binding the microtubule altogether

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. Allows protofilaments to run nearly parallel to the microtubule axis, providing a straight track for motors
B. Eliminates the GTP cap required for dynamic instability
C. Forces protofilaments into a strongly left-handed supercoil
D. Maximizes the microtubule diameter for maximal cargo capacity

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. The stabilizing GTP cap is lost, exposing GDP-tubulin that favors protofilament peeling
B. GTP hydrolysis on -tubulin releases the lateral bonds
C. Lateral bonds strengthen as GDP-tubulin accumulates
D. Free tubulin concentration rises above the critical concentration

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. Directly change the number of protofilaments in the lattice
B. Convert -tubulin into -tubulin over time
C. Provide the chemical energy for motor stepping
D. Modulate the recruitment and processivity of specific motors and MAPs on microtubule subsets

53 Taxol (paclitaxel) is a chemotherapeutic that binds -tubulin. Its anti-mitotic effect arises because taxol:

Microtubule structure Hard
A. Stabilizes microtubules and suppresses dynamic instability, blocking mitotic spindle function
B. Severs microtubules into short non-functional fragments
C. Sequesters free tubulin dimers to prevent any polymerization
D. Depolymerizes microtubules by stripping the GTP cap

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. Force-dependent unfolding of talin/exposure of cryptic sites reinforcing focal adhesions and activating YAP/TAZ signaling
C. Diffusion of ECM proteins into the nucleus to bind DNA directly
D. Passive osmotic swelling that ruptures the nuclear envelope

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. Osteogenic differentiation driven by high cytoskeletal tension and YAP activation
B. Complete loss of differentiation potential regardless of stiffness
C. Adipogenic differentiation due to low actomyosin tension
D. Neurogenic differentiation favored by minimal contractility

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. ATP hydrolysis within the channel driving conformational opening
B. Membrane tension flattening its curved, blade-like domains to open the pore
C. Phosphorylation of its C-terminus by a mechanosensitive kinase
D. Ligand binding at an extracellular pocket that triggers channel 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. Preventing angiogenesis and thereby starving the tumor
B. Reducing intracellular tension so cells become quiescent
C. Physically blocking all cell migration through the tissue
D. Enhancing integrin clustering and mechanosignaling that boost proliferation, survival, and invasion

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. Triggers sustained NF-B inflammation and endothelial disarray
B. Blocks nitric oxide production and raises vascular tone
C. Causes endothelial cells to detach from the basement membrane
D. Aligns cells with flow and promotes anti-inflammatory, vasodilatory signaling (e.g., eNOS/NO)

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. Motor neurons fail to release acetylcholine at the synapse
C. Muscle cells can no longer produce ATP for contraction
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. Depolymerize microtubules that contact the nucleus
C. Physically couple the cytoskeleton to the nuclear lamina, transmitting force to reshape chromatin and nuclear signaling
D. Generate ATP-driven force for chromosome movement during mitosis