week 5 Flashcards

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1
Q

how are cells held together?

A
  • you need intracellular and extracellular adhesion
  • proteins inside and outside will hold things in place
  • ## cell-cell adhesion proteins
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2
Q

what moves in the cell?

A
  • organelles, cells and tissues
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3
Q

how do tings move in cells and how do cells move

A

cytoskeletal proteins

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4
Q

cytoskeleton

A
  • intricate network of protein filaments that extend throughout the cytoplasm
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5
Q

what makes up the cytoskeleton?

A
  • microfilaments
  • microtubles
  • intermediate filaments
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6
Q

microfilaments

A
  • 7-9 nm width
  • actin subunits
  • this is the thinnest component
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7
Q

mictotubules

A
  • alphabeta- tubulin dimer subunits
  • this is the thickest component
  • 25 nm width
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8
Q

intermediate filaments

A
  • various subunits
  • 10 nm width
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9
Q

how can the cytoskeleton be visualized

A
  • through immunofluorescence
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10
Q

DNA length. of one turn?

A
  • 10 nm = 100 A
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11
Q

is there any empty space in a cell

A

NO- solvents like cytoplasm or RBC floating blood stream

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12
Q

microtubules

A
  • polymer of alpha and beta tubulin
  • 25 nm in diameter
  • can be up to 100s of micrometers long
  • organize the
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13
Q

alpha and beta tubulin

A
  • monomer of microtubules
  • 55 kDa each
  • alpha-beta dimer
  • have polarity
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14
Q

why does the alpha beta dimer have polarity

A
  • polyervizes faster on the positive side
  • the positive is the beta tubulin end
  • the negative is the alpha tbulin end
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15
Q

how long is one dimer of alpha beta tublin

A

8 nm

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16
Q

how is a seam created in microtubule protofilaments

A
  • not folding properly, all the subunits ar not lined up
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17
Q

protofilaments

A
  • dimers of the Dublin subunits strung together
  • long strands
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18
Q

how many protofilaments ar included in the hollow tubes of mictobtules

A

13

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19
Q

what are the largest cytoskeletal filaments that we discuess

A

microtubules

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20
Q

in what form do the subunits have to be in, in order to polyermize

A

in GTP form
- the order of polymerization is alpha beta alpha beta

21
Q

dimeric tubulin subunit

A
  • very stable (dimer is not easily separated)
  • alpha tunulin binds gTP only
  • beta tubulin can hydrolyze GTP (can be bound to either)
  • beta gTP is hydrolyzed as the protofilament polymer grows
22
Q

how can MT protofilaments be arranged

A
  • singlet
  • doublet
  • triplet
23
Q

singlet

A
  • found in cytoplasm
  • 13 protofilmanets form a single tube of 25 nm.
  • 13 protofilaments
24
Q

doublet

A
  • made up of two microtubules
  • 13 A protofilaments and 10 B protofilaments subunits
  • in cilia nd flagella
25
Q

mictorbuulse in cytoplasm

A
  • the cytoplasm of all cell have these
  • e.g. nerve axon
  • singlet mmicrotbules
26
Q

axonemela microtubules

A
  • specific organization and type of microtbubule found in cilia and flagella
  • doublet microtubules
27
Q

what do singlet mictobrubles in cytoplasm and nerve axons fo

A

transport things along axons to nerve cell boies

28
Q

MTOC

A
  • main one = centrosome
  • where microsomes polyermize from
29
Q

centrosome

A
  • contains centrioles
  • centrioles are not found in plantscen
30
Q

centriole

A
  • triplet microtubules
  • two triplets that are ninety degrees to erah other
  • striplets = pretty stable, and dont really polyermzie or depolyermize, which makes centrioles stable.
  • has pericentriolar matrix
31
Q

mother and daughter centrioles

A
  • centrioles must replicate during mitosis
32
Q

pericentriolar matrix

A

has proteins like gamma tubulin, augmen, - surrounds the centrioles

33
Q

augment and gamma tubulin

A
  • found in the pericentrioar matrix
  • form complexes that allow the singlet microtubules to polyermize
34
Q

in what direction are singlet microtubules polyermized

A
  • with plus end going away from the centrosome
  • the e end is in the pericentrular matrix
35
Q

How many triplets in a centriole ring?

A

9

36
Q

gamma tubulin ring complex

A
  • provides nucleating sites for mcirotiubules.
  • facilitates microtbubuel branching with agumin
  • gamma tubulin ring complex = nucleating site
37
Q

where does polymerization start

A
  • gamma tubulin and gamma tubulin ring complex, located at negative end
38
Q

where do microtubule assembly and disassembly occur

A

at plus end

39
Q

what does a nucleation site do

A

accelerates initial polyermization

40
Q

nucleaiton

A
  • ## micotunule can grow on already existing microtubules (these are used a a nucleus)
41
Q

why is the - end never capped

A
  • because ti is capped
  • but plus end will grow and shrink
42
Q

why is elongating/poymerizing from single subunits so time consuimg/

A
  • must form nuclei
  • adding nuclei already means no need for formation, means faster poylermization, if enough subunits to be above the critical concentration
43
Q

actin example of closed system polyermization

A
  • add actin monomers above citric concentration
  • slow growth initially, because monomers must come together to form nuclei
  • after that, can get rapid elongation.
  • if u add nuclei from the start, no lag phase (.e.g having gamma tubullin ring complex which acts a. nucleus in the centrosome)
44
Q

dynamic instability

A

oscillations in length
- cells need this in order to get to different locations

45
Q

what does dynamic instability depend on

A
  • the presence or absence of a GTP beta tubulin cap
46
Q

microtubule disruption drugs

A

colchicine
taxol
anticancer drugs

47
Q

colchicine

A

depolyermization of all teh singlet microtubules

48
Q

taxol

A

stabilizes