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100 question-and-answer flashcards summarizing key concepts on cytoskeletal filaments, motor proteins, cell junctions, and related diseases.
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Microfilaments (actin), intermediate filaments, and microtubules.
To provide shape, mechanical strength, and an intracellular ‘highway’ for organelle and vesicle movement.
Actin microfilaments.
Intermediate filaments.
Microtubules.
Vimentin, keratin, neurofilaments, and desmin (muscle-type vimentin).
Nuclear lamins.
An α-helical polypeptide that forms a coiled-coil dimer.
Two monomers.
A tetramer (two dimers side-by-side).
They align antiparallel and staggered, then eight such strands twist together.
Their rope-like, staggered tetramer structure resists stretching (high tensile strength).
Desmosomes.
The extensive lateral packing of staggered tetramers.
They provide rigidity and shape to the nuclear envelope.
Progeria syndrome.
Kinesins and cytoplasmic dyneins.
Toward the microtubule + (plus) end, usually toward the cell periphery.
Toward the microtubule − (minus) end, usually toward the cell interior/centrosome.
A heterodimer of α-tubulin and β-tubulin.
Thirteen.
GTP.
β-tubulin.
The centrosome (microtubule-organizing center).
γ-Tubulin ring complex (γ-TuRC).
Dynamic instability.
Alzheimer’s disease.
Retrograde dynein-mediated transport along axonal microtubules.
Taxol (paclitaxel).
Approximately 7 nm.
ATP (or ADP after hydrolysis).
The Arp2/3 complex.
Formin.
Profilin.
Filopodia.
Lamellipodium.
The contractile ring.
Myosin II.
It detaches from actin (leading to relaxation).
Release of inorganic phosphate after ATP hydrolysis triggers the power stroke.
Tight junction.
Claudins and occludin.
Adherens junction.
Calcium (Ca²⁺).
E-cadherin.
N-cadherin.
Homophilic binding.
Cell sorting (tissue segregation and morphogenesis).
β-Catenin (together with α-catenin).
Vinculin.
Desmosome.
Desmoglein and desmocollin.
Desmoplakin (with plakoglobin and plakophilin).
Hemidesmosome.
Focal adhesion (actin-linked cell–matrix junction).
Six connexins.
A gap junction channel.
Approximately 1,000 Da.
Inside-out signaling via talin, kindlin, or RIAM binding to the β-integrin tail.
Talin (often followed by vinculin).
Selectins (E-, P-, or L-selectin).
ICAM (Intercellular Adhesion Molecule).
Rac (also Rho family members).
They provide structural support for the centrosome and help organize microtubule nucleation.
The − (minus) end.
The hollow interior space inside the 13-protofilament cylinder.
The Arp2/3 complex (acts as a nucleation core).
The actin cortex.
Most myosins, including myosin VI, move toward the minus end (unlike others that move toward plus).
ATP.
They have distinct + (barbed) and − (pointed) ends.
They become ADP-actin, lowering affinity and favoring dissociation at the − end.
Epithelial absorptive surfaces such as the small intestine.
The perijunctional actin belt.
About 70 degrees.
Rabies (viral spread to the brain via dynein transport).
Microtubules (organized in a 9 + 2 arrangement).
Nine triplet microtubules arranged in a cylinder.
The mitotic spindle (kinesin- and dynein-based motor complexes on microtubules).
The protofilaments curve outward, causing rapid depolymerization (catastrophe).
Their staggered, nonpolar rope-like architecture distributes tensile stress.
Intermediate filaments.
Intermediate filaments (e.g., keratin in skin).
α-Actinin and associated proteins.
The + (plus/barbed) end.
It contracts actin filaments, pulling the trailing edge forward.
Claudins.
Helps regulate barrier properties and junction stability.
Via scaffolding proteins such as ZO-1, ZO-2, and ZO-3 containing PDZ, SH3, and GK domains.
The ZO (zonula occludens) protein family.
Interconnected rows of claudins/occludin that form the tight junction barrier between adjacent cells.
Laminin (and type IV collagen in basal lamina).
Plectin and BP230 (bullous pemphigoid antigen 1).
It stabilizes microtubules, preventing depolymerization and blocking mitosis.
It binds actin-ADP, promotes ADP–ATP exchange, and delivers ATP-actin to the + end.
Hyperphosphorylated Tau detaches from microtubules, causing their disassembly.
The stochastic switching of microtubules between phases of growth and rapid shrinkage.
The + (plus) end.
Selectins mediate initial rolling adhesion, then integrins bind ICAMs for firm arrest and transmigration.