Term 1- Lec 9- Cytoskeleton & Vesicular Transport Flashcards

1
Q

Intermediate filaments: •Size
•shape
•composition
•function

A
  • 8-10 nm (middle sized fil)
  • Rope-like
  • Various protein filaments
  • Helps to maintain structure of the cell
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2
Q

Microtubules: •size
•shpe
•composition
•function

A
  • 20-25 nm
  • Hollow cylinder
  • Polymer of tubulin dimers—∂ & ß
  • Intracellular transport via motor proteins, chromosome segregation, and cilia and flagella
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3
Q

Actin Filaments (Microfilaments): •size
•shape
•composition
•function

A
  • 6-8 nm
  • Double-stranded hilical shape
  • Polymer of G-actin
  • Structural, muscle contraction
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4
Q

Intermediate filaments are anchored at

A

desmosomes and hemidesmosomes—sites of stress

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5
Q

Intermediate filaments in epithelium

A

Keratin

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6
Q

Intermediate filaments in non-epithelium

A

Vimentin

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7
Q

Intermediate filaments in neurons

A

Neurofilaments

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8
Q

What is the structural polarity of an intermediate filament?

A

Intermediate filaments do not have structural polarity

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9
Q

Mutations in keratin genes that result in abnormal assebly of keratin filaments in epidermis:

A

Epidermolysis Bullosa Simplex (EBS)

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10
Q

Mutations in neurofilaments that cause abnormal accumulation and assembly cause progressive loss of motor neurons:

A

Amyotrophic Lateral Sclerosis (ALS, or Lou Gehrig’s disease)

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11
Q

Microtubules are anchored at:

A
  • MTOC (centrosome, minus ends)
  • Capping proteins (plus ends)
  • Spindle poles
  • Basal body of cilia and flagella
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12
Q

Microtubules bind to which nucleotide

A

GTP—has GTP Catalytic activity

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13
Q

Monomers that make up microtubules

A

∂ and ß tubulin (form heterodimers)

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14
Q

What is the structural polarity of microtubules

A

1 minus and 1 plus end per microtubule

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15
Q

What motor proteins are associated to Microtubules

A
  • Kinesin—toward plus end (plasma membrane)

* Dynein—toward centrosome (into heart of cell)

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16
Q

Describe Dynamic Instability of microtubules

A

GTP-bound heterodimers of ∂ and ß tubulin concentrations drive this. If the dimers are added faster than the previous layer can be hydrolyzed off, then the microtubule grows. Vice versa for shrinking.

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17
Q

What stabilize microtubules at the + end?

A

Capping proteins

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18
Q

What event polarizes a cell

A

The capping of the + end of microtubules

19
Q

What motor proteins are associated to microtubules and enzymatic activity do they exhibit?

A

Kinesin and Dynein. They both exhibit ATPase activity. Walking along the microtubules requires ATP.

20
Q

What is the motor protein in cilia and flagella?

A

Axonemal dynein

21
Q

Absence of motor protein in flagella and cilia:
• Name of the disorder
•Motor protein it is deficient of
• What are the cinical consequences

A
  • Kartagener Syndrome
  • Axonemal dynein is deficient
  • Leads to male sterility and chronic resiratory infection
22
Q

Function of Actin filaments or microfilaments

A
  • Microvilli
  • Muscle contraction
  • Lamellipodia and filopodia for movement
23
Q

What anchors actin filaments/microfilaments?

A

Adherens junctions and Focal adhesions

24
Q

Microfilaments bind to what nucleotide?

A

ATP—has ATP catalytic activity

25
Q

Monomers of microfilaments

A

G-actin

26
Q

Do microfilaments have structural polarity?

A

Yes, - and + ends

27
Q

Associated motor proteins with microfilaments

A

Myosin I and Myosin II

28
Q

What controls microfilament dynamic instability?

A

ATP binding and hydrolysis. ATP binding favors polymerization, ATP hydrolysis favors depolymerization

29
Q

What are the 3 structures formed by Microfilaments and where are they?

A
  • Parallel bundles—Microvilli and filopodia
  • Contractile Bundles—Stress fibers @ focal adhesions
  • Networks—Cell cortex: determines cell shape
30
Q

Actin’s role in muscle contraction

A

Myosin II (using ATPase activity) pull actin filaments to the center of the sarcomere

31
Q

Anctin’s role in intracellular transport

A

Myosin I walks along the actin filaments toward the plus end.

32
Q

Vesicular Transport

A

Transportation of newly synthesized proteins move via vesicales along the ER-Golgi path

33
Q

Organelle specific proteins:

A

Include ER-, Golgi- and Lysosomal-specific proteins

34
Q

Plasma membrane proteins and secretory proteins:

A

Mediated through exocytosis.

35
Q

What tag assures that a protein will return to the ER?

A

KDEL

36
Q

How do ER-destined proteins return from the golgi?

A

A membrane receptor in the CIS golgi packages them and returns them in retrograde vesicles

37
Q

What type of enzymes do lysosomes contain?

A

Acid hydrolytic enzymes—nucleases, proteases, glycosidases, lipases, etc.

38
Q

What is the pH of the lumen of a lysosome, and how is it maintained?

A

Lysosomal lumen is acidic. The acidic pH is maintained by a H-ATPase, which pumps H+ into the lysosome.

39
Q

All lysosome destined proteins are marked by

A

Mannose-6-P (M6P)

40
Q

How does I-cell disease occur?

A

Deficiency of the enzyme that adds M6P to the lysosomal proteins

41
Q

Early and Late endosomes

A

Early: Conatins macromolecules that are waiting to be borken down.
Late: Contains an increasing amount of hydrolytic enzymes. As more enzymes arrive, it will become a lysosome

42
Q

Lysosomal storage diseases

A

Most involve the dysfunction of lysosomal hydrolases, impairing degradation. Some involve vesicular traffic or the biogenesis of lysosomal proteins (I-cell) causing storage disorders

43
Q

What always causes secretory granules to be released?

A

Ca2+