Motor Proteins and Muscles Flashcards

1
Q

structure for moving in single-celled animals vs multicellular

A

use motor porteins and cytoskeleton!
single-celled use flagella and cilia
multicellular use skeleton and muscles

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

cytoskeleton

A

network of filaments that support plasma membrane, give cell overall shape, correct positioning of organelles, tracks for transport of vesicles, allow cells to move
microfilaments, intermediate filaments, microtubules

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

motor proteins

A

microfilaments and microtubules are tracks for their movement
motor proteins use energy in the form of ATP to walk along te filaments

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

microfilaments aka actin filaments

A

actin portein subunits, tracks for myosin motor portein

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

sarcomeres

A

organized structures of overlapping filaments of microfilaments -> control muscle movement

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

microtubules

A

tubulin proteins, hollow, straw-like tube for tracks for kinesin and dyenin motor proteins; important for cellular structural integrity and cell movement; cell movement via cilia and flagella (dynein) while kinesin is for movement of vesicles and intracellular cargoes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Flagella

A

long, hair-like structures that extend from cell surface to move entire cell; sperm; usually one or few on a cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Motile cilia

A

shorter, large numbers on the cell surface; cilia in upper respiratory system moves dust out towards nostrils

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

9 +2 Array

A

cilia and flagella - 9 pairs of microtubules in a circle with 2 other tubes in the cross-section
pairs are connected by protein bridges and dyneins that move along the microtubules - causes the flagellum or cilium to beat; causes the entire structure to bend

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

3 types of muscle tissues

A

skeletal, smooth, cardiac

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

skeletal muscle

A

control locomotion and any conciously controlled movement
voluntary muscle
long and cylindrical, striped or striated appearance -> regular arrangement of contractile proteins (actin and myosin); also multiple nuclei in one cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

smooth muscle

A

hollow organs like intestines, stomach, urinary bladder, passages like respiratory tract and blood vessels
not voluntary control - involuntary muscle
no striations
one nucleus per cell

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

cardiac muscle

A

heart only - pump blood and maintain blood pressure; also involuntary muscle

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

pacemaker cells

A

spontaneously initate cardiac muscle contraction so that heart can beat without nervous system (nerves can slow or speed up heart rate tho..)
one nucleus per cell, branches

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

intercalated disks

A

allow rapid passage of action potentials from one cardiac muscle cell to the next

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

skeletal muscle fiber

A

single skeletal muscle cell - incredible large, up to 30 cm

17
Q

myofibrils

A

within each muscle fiber
long cylindrical structures that lie parallel to muscle fiber
contains repeating units of sarcomeres (contractile units); give muscles a banded appearance

18
Q

myosin

A

thick dark filament

19
Q

actin

A

thin light filament

20
Q

Z discs or lines

A

structures at the end of each sarcomere where actin filaments are physically anchored

21
Q

M line

A

center of the myosin filament

22
Q

when the sarcomeres contract individually:

A

myofibrils and muscle cells shorten BUT the actin and myosin fibers are the same length they just slide past each other

23
Q

tropomyosin and troponin

A

strands of tropomyosin block the binding sites and prevent actin-myosin interactions when the muscles are at rest
troponin regulates tropomyosin
calcium ions regulate troponin: binding calcium to troponin causes the troponin-tropomyosin complex to move away from myosin binding sites on the actin filament, allowing myosin to bind to actin and initiate contraction

24
Q

sliding filament model

A

the thick and thin filaments slide by one another causes sarcomere to shorten while the filaments remain the same length
done by the cross-bridge cycle of actin-myosin binding

25
Q

cross-bridge cycle

A
  1. myosin binds to ATP but it is not bound to actin
  2. Myosin turns ATP into ADP and inorganic phosphate and myosin is still bound to both molecules; now it can attack to myosin-binding site on actin if available (remains in this state if there even aren’t any available)
  3. myosin releases inorganic phosphate, still bound to ADP, intiates the Powerstroke and pulls the actin filament towards the M line and causes muscle contraction
  4. then ADP is released and it remains stuck to the actin filament until another ATP molecule is bonded - depletion of ATP due to muscle fatigue will cause muscles to remain locked in contracted state
26
Q

importance of troponin and tropomyosin

A

determine where myosin binds to actin or not by blocking the binding sites without nervous input during a resting state
calcium changes conformation and makes the binding site available

27
Q

sarcoplasmic reticulum

A

endoplasmic reticulum in muscle cells where calcium is stored; nervous system regulates availability of calcium

28
Q

neuromuscular junction or synapse

A

structure that receive signals from efferent neurons to control muscles
receives acetylcholine as its neurotransmitter -> intiates an action potential like in a normal nueron with depolarization; spreads through structures T-tubules which carry action potential to SR -> release calcium
afterwards when muscle cell is returning back to membrane potential, calcium is pumped back into SR