Cell motility Flashcards

1
Q

the motor proteins Kinesin and Dynein are microtubules or microfilaments?

A

microtubules

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2
Q

the motor protein myosins are microtubules or microfilaments?

A

microfilaments

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3
Q

what is an example of a cell that moves?

A

neutrophils: move to site of infection and engulf foreign invaders

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4
Q

intracellular components move: microtubules of the mitotic spindle play a role in the ??? of chromosomes during cell division

A

separation

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5
Q

To generate movement, MTs and MFs provide a scaffold for motor proteins that produce motion at the ??? level

A

molecular

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6
Q

the following describes Microtubule-based motility or microfilament based motility?
- transport of organelles and vesicles
– Formation of mitotic and meiotic spindles
– fast axonal transport in neurons
– sliding of MTs in cilia and flagella

A

microtubule-based motility

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7
Q

the following describes Microtubule-based motility or microfilament based motility?
- muscle contraction
– cell shape changes and migration
– cytoplasmic streaming

A

microfilament-based motility

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8
Q

motility systems couple ATP hydrolysis to changes in shape and attachment of ??? i.e. they convert chemical energy into mechanical work

A

the motor proteins

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9
Q

motility systems undergo cycles of ATP hydrolysis, ADP release and aquisition of new ATP, driven by ???

A

motor proteins

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10
Q

TRUE or FALSE: motor proteins have common structural features and can move along cytoskeletal filaments for significant distances

A

TRUE

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11
Q

motor proteins move BI-directionall or UNI-directionally (?) across their cytoskeletal track in a stepqise manner. dynamic instability regulates this signalling

A

unidirectionally

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12
Q

the lever domain of a motor protein transduces ???

A

conformational change

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13
Q

Kinesins and Dyneins move along microtubules, transporting organelles and vesicles toward the NEGATIVE or POSITIVE (?) end, considered ‘inbound’ whilst towards the opposite end is ‘outbound’

A

negative/minus end

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14
Q

Axonal transport: proteins produced in the cell body are transported to the nerve ending = FAST or SLOW?

A

fast

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15
Q

fast axonal transport involves packaging proteins into vesicles for transport by ??? and cytoplasmic dynein

A

kinesin I

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16
Q

Kinesin I or cytoplasmic dynein is responsible for the following?
- Involved in ATP‐dependent transport toward the positive end (outbound)
- Called anterograde axonal transport

17
Q

Kinesin I or cytoplasmic dynein is responsible for the following?
- Moves particles in the opposite direction to the negative end (inbound)
- Called retrograde axonal transport

A

Cytoplasmic dynein

18
Q

Kinesins move towards the plus end of MTs and consist of two dimerised heavy chains and two light chains. The heavy chains contain globular domains that attach to ???

19
Q

ADP bound head of DYNEIN or KINESIN (?) binds to tubulin and ADP is displaced for ATP = results in rear head flipping forward which affects the conformation, flipping the linker forward and the lagging head with it to the next tubulin to which it binds. Cycle repeats

20
Q

Kinesin can move long distances along Microtubules before detaching from it by releasing bound ??? and acquiring a new ATP so that the cycle repeats.

21
Q

dyneins are a family of minus end-directed microtubule motors structurally unrelated to the kinesins. They are the LARGEST or SMALLEST motor protein?

22
Q

Cytoplasmic or axonemal dynein (?) are associated with a protein complex called dynactin, which helps link dynein to cargo

A

cytoplasmic

23
Q

Cytoplasmic or axonemal dynein (?) are specialised for the rapid and efficient microtubule sliding movements that drive the beating of cilia and flagella

A

axonemal dyneine

24
Q

dyneins follow the general rule of coupling ATP hydrolysis and ??? change to microtubule binding and unbinding resulting in a power‐stroke forward

A

conformational

25
dyneins can jog in place, causing the whole microtubule to roll along beneath it. This often occurs in conjunction with ??? of the MT
depolymerisation
26
how are chromatids separated and dividing cells separated during mitosis?
the action of dyneine jogging in place, causing the MT to roll beneath it
27
membrane extensions of the ER can be moved along microtubules. The vesicles to and from the golgi complex are carried by microtubule ??? on microtubules
motor proteins
28
movement of membrane extensions of the ER is based on polarity: - Kinesin moves golgi to ER and Golgi to ??? (exocytosis) - Dynein moves ER to golgi and ??? to golgi (Endocytosis)
cell membrane
29
myosin is an ATP-dependent motor that interacts with and exerts force on ???
actin microfilaments
30
all ??? have at least one heavy chain with a globular head group attached to a tail of varying length
myosins
31
myosin uses a cycle of structural changes to walk along ???
actin filament
32
Myosin contraction cycle: 1. attached to actin 2. released by binding ATP which causes reduced affinity for actin 3. cocked, conformational change causes lever arm to swing, ATP is ??? 4. rebinding: myosin head binds weakly to new site 5nm along actin filament 5. power stroke: Pi is released and myosin becomes tightly bound 6. force generating: cycle begins again
hydrolysed
33
what is the difference between myosin and kinesins? - ??? operate alone or in small numbers to transport vesicels over large distances - ??? move short distances but operate in large arrays
KINESIN MYOSIN II
34
myosin II pulls arrays of actin filaments together = rapid and efficient contraction of ???
muscle cells
35
??? muscle fibres are huge single cells produced from the fusion of manyb cells, the cytoplasm of which is filled with myofibrils that are repeating units of contractile units (sarcomeres)
skeletal
36
Non-muscle cells crawl/move using ??? and/or filopodia
lamellipodia
37
non-muscle cell movement involves protrusion produced by ??? of the branched actin network at leading edge
polymerisation
38
non-muscle cell movement involves attachment to substratum proteins via focal adhesions and tension to detach the ??? edge
trailing
39
Non‐muscle cells move via polymerisation of actin at leading edge, attachment to substratum, actin‐myosin contraction, and retraction of rear by ???
depolymerisation