Cytoskeleton Flashcards

1
Q

Which secretory pathway doesn’t need a signal? What types of stuff gets transported on this pathway?

A

Constitutive secretory pathway. Add receptors to plasma membrane / secreting proteins without special features

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2
Q

Which secretory pathway runs through a signal cascade? What goes through it?

A

regulated secretory pathway. Sends out secretory proteins (have signals on them).

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3
Q

What signal marker diverts proteins to lysosomes?

A

Mannose 6-phosphate.

Do receptors go to lysosomes too? check in book

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4
Q

What is another word for actin filaments?

A

microfilaments

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5
Q

How many strands to actin filaments have? What are the strands?

A

Two strands. Helical polymers of the protein actin.

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6
Q

What important thing does an actin monomer have in a central cleft?

A

ATP or ADP

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7
Q

What designates the minus and plus end of an actin filament?

A

The orientation of subunits. They all have the same orientation

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8
Q

What protein causes actin to pack tightly?

A

fimbrin. Forms parallel bundle (orientation of all filaments is the same in terms of + and -)

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9
Q

Why does fimbrin packing actin tightly matter?

A

Tight packing prevents myosin II from entering bundle

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10
Q

What protein loosens up actin?

A

a-actinin. Forms contractile bundle (orientation of actin filaments is opposite in terms of + and -)

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11
Q

If there is no actin at all, how fast will it form compared to growing pre-existing actin?

A

Slower (lag phase)

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12
Q

What is it called when actin filaments aren’t growing or contracting?

A

equilibrium phase, steady state. Happens at Cc (critical concentration)

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13
Q

What needs to happen for actin filaments to be elongated?

A

Subunits have to be above critical concentration

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14
Q

What is treadmilling?

A

Subunits are getting removed at - end

Subunits are getting added at + end

Both happens at the same rate

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15
Q

At what concentration of filaments does treadmilling happen?

A

Intermediate concentration

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16
Q

What types of subunits do actin filaments contain?

A

T form (soluble)

D form

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17
Q

T subunits are at their critical concentration

D subunits are at their critical concentration

Is there the same number of subunits?

A

No. Cc of T requires less subunits

Cc of D requires more subunits

Treadmilling happens when you’re both above the critical concentration of T and below the critical concentration of D

Why? (Read book on this)

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18
Q

Why must proteins released to extracellular space need to be soluble?

Where do these proteins come from? How are they transported?

A

Soluble because that way they can get through membrane

Come from trans golgi, transported in lipids which become part of plasma membrane.

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19
Q

Which pathway are neurotransmitters exocytosized through? Why?

A

Regulated secretory pathway.

They need to wait by the plasma membrane in secretory vesicles

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20
Q

Which pathway are most membrane lipids and membrane proteins added through?

A

Constitutive secretory pathway

Lipids come from the vesicles themselves, membrane proteins attached to vesicles during travel

21
Q

Where in relation to the ER / cytoplasm are the cisternae of the trans golgi network?

Cis golgi network?

A

Trans is closer to the cytoplasm

Cis is by the ER

22
Q

What makes up a single intermediate filament coiled-coil dimer?

A

Two dimers wrapped around each other

antiparallel (n-terminus next to c-terminus)

23
Q

What makes up a single intermediate filament? How do they grow?

A

Two coiled-coil dimers form a tetramer by lining up (c-terminus next to c-terminus, staggered)

8 tetramers line up in parallel. 32 individual a-helical coilds per filament.

To grow, another circular set of 8 filaments adds on to the end

24
Q

Where can a dense network of intermediate filaments be found? Why? What are they called?

A

Nuclear lamina (called nuclear lamins).

Anchorage site for chromosomes / nuclear pores

25
Q

What is keratin? Where do you see it? What’s it made of?

A

Type of intermediate filament made up of acidic + basic subunits in each coiled-coil dimer

See it in hair, nails, etc

26
Q

What is the process of actin forming its initial aggregate that can then grow called?

A

nucleation

27
Q

What are the T and D forms of actin subunits?

A

T form = ATP inside

D form = ADP inside

28
Q

Is it harder to separate a D subunit or T subunit of actin?

A

D subunit. Energy of hydrolysis gets stored in polymer when ATP>ADP

29
Q

What form are soluble actin subunits in?

Polymers?

A

Generally T form

Polymers a mixture of T and D, but more D the longer they’ve existed

30
Q

What protein causes closer packing? What is the result of that?

What protein causes looser packing? What is the result?

A

Closer packing: fimbrin. This close packing excludes myosin, so parallel actin filaments with fimbrin can’t contract

Looser packing: a-actinin. Allows binding of myosin, sow formation of antiparallel contractile actin bundles.

31
Q

What kinds of things do actin accessory proteins regulate?

A

Change formation ability (nucleation)

Speed actin forms (adding to + end)

Size of filament (e.g. capping protein)

Stability (more or less rigid)

Number of filaments

Geometry (bundling, crosslinking like in neuron growth, attachment to plasma membrane)

32
Q

What does a myosin II motor protein look like?

What are the functions of each component?

A

heavy chain: Neck with two heads (force-generating machinery)

heavy chain: Long coiled-coil (heavy-chain dimerization)

light chains

C terminus

33
Q

What are multiple myosin filaments together called?

What do they look like?

A

Myosin II bipolar thick filament

Myosin tails making a fiber, heads on the outside

Fiber has two parts, with heads on each side, pointed towards each other:

o== ==o

34
Q

Which direction does myosin walk along actin? How?

How does this turn into myosin moving muscle?

A

Myosin head hydrolizes ATP
Uses that energy to walk towards + side of actin

Bipolar thick filament moves oppositely oriented actin filaments towards each other

35
Q

How can small bipolar myosin filaments quickly be formed?

What is the purpose of this?

A

Inactive myosin: light chains dephosphorylated

Active myosin: light chains phosphorylated

Myosin activation causes head to start binding actin, tail to start forming bipolar filaments

Purpose: Control non-muscle contractile bundles. Give mechanical support to cells

36
Q

What is the purpose of Myosin V? (two-headed, large step size)

A

Transport stuff along actin by walking along filaments towards + end

37
Q

What direction do intermediate filament monomers assemble?

A

Parallel

38
Q

How rigid is a microtubule compared to other cytoskeleton components?

A

More rigid than actin

39
Q

What are the linear strings of tubulin that make up microtubules called?

What are they composed of?

How many are there?

How are they organized?

A

Protofilaments

…alpha tubulin - beta tubulin - alpha tubulin…

13 make up a microtubule

They connect with each other laterally to make a circle

40
Q

What’s the inside of a microtubule called?

A

microtubule lumen

41
Q

Is GTP more tightly bound in a- or B- tubulin?

Why does this matter?

A

alpha tubulin

GTP can never be hydrolized to GDP in a-tubulin, only in B-tubulin

42
Q

Why are microtubules so stiff?

(same reason they only add / get removed at the ends)

A

Protofilaments aren’t right next to each other, they’re staggered a bit

Because of this, each subunit has multiple connections with other subunits

This makes for very high energy in the middle of microtubules

43
Q

Which direction on a microtubule, +-, do dyneins travel?

A

Towards the - end

44
Q

How fast does GTP hydrolysis occur in free B-tubulin vs B-tubulin in microtubules?

If GTP is hydrolyzed to GDP, what happens to B-tubulin?

A

Slow in free tubulin

Fast in microtubule

Tubulin relaxes into curved conformation, allowing catastrophe

45
Q

What complexes do microtubules grow from?

What end of microtubule goes away from centrosome?

A

y-tubulin ring complexes of centrosome

+ end goes out

46
Q

What is the material in the MTOC called? What is another name for it?

A

Material = pericentriolar material

MTOC = centrosome in animal cells (one per G1)

47
Q

What is the actual function of centrioles?

A

Organize centrosome matrix

Become basal body of cytoskeletal apparatus in cilium / flagella

48
Q

Where are the N- and C- terminuses of kinesin?

Why is kinesin-14 different?

A

N-terminus: Mostly the motor domain (head) except for kinesin 14

Kinesin-14 has N terminus on opposite ends of motor domains, and goes opposite direction (towards - end)

49
Q

What are melanocytes? Why are they important?

A

Pigment granules, shows that kinesins/dyneins can be controlled by hormonal changes

Less cAMP = inactivated kinesin, dynein drags granules towards center (change fish color)

More cAMP = kinesins (both) activated, granules spread out (kinesins stronger)