BI203 Lecture 17: Protein Sorting and Transport - Slides 88-104 (Vesicle Fusion, Endosomes, and Lysosomes) Flashcards

1
Q

Two steps when a vesicle arrives at its destination:

A

docking, fusion

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2
Q

Vesicle docking is controlled by the ___ family of proteins.

A

Rab

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3
Q

Specific Rabs associate with specific transport vesicles & target membranes.

Rabs recruit ___ ___ ___ (MTFs).

Protein-protein interactions between ___ ___ ___ (MTFs) mediate vesicle docking at target membranes.

A

membrane tethering factors (MTFs)

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4
Q

Fusion of a transport vesicle with its target:

  1. The vesicle must recognize the correct ___ membrane.
  2. Vesicle and target membrane must ___, delivering the contents to the target organelle.
A

target, fuse

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5
Q

Interaction between transport vesicles and target membranes is mediated by ___ ___ ___ (MTFs) and small-GTP binding proteins (___ proteins).

A

membrane tethering factors (MTFs), Rab

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6
Q

Vesicle Rab proteins in the active ___ state bind membrane tethering factors.

A

GTP-bound

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7
Q

Tethering factors also bind coat proteins, and may stimulate formation of complexes between transmembrane proteins called ___.

A

SNAREs

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8
Q

Formation of complexes between vesicle and target SNAREs is required for ___.

A

fusion

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9
Q

___ pairing provides the energy to bring the two bilayers close enough to destabilize them and fuse.

A

SNARE-SNARE

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10
Q

SNARE proteins have a central coiled-coil domain.

This domain binds to other coiled-coil domains and zips the SNAREs on ___ and ___ membranes together.

This brings the 2 membranes into direct contact and leads to ___ of the lipid bilayers.

A

vesicle, target, fusion

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11
Q

Vesicle ___ and Target ___ interact with each other to form “coiled-coils”.

The coiling of the ___ around each other drives the membranes against each other.

A

v-SNAREs, t-SNAREs, SNAREs

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12
Q

Lysosomal function is dependent on an internal pH of ___.

Lysosomal ___ ___ help maintain this acidic pH.

A

5, proton pumps

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13
Q

Lysosomes need a pH of 5 because ___ ___ are only active at a pH of 5.

A

acid hydrolases

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14
Q

___ - Membrane-enclosed organelles that contain enzymes to break down all types of biological polymers.

They are the digestive system of the cell.

They can vary in size and shape depending on the materials that have been taken up for digestion.

A

lysosomes

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15
Q

Acid hydrolases are active inside the lysosome, but NOT in the ___. This is to prevent uncontrolled digestion of cell contents if the lysosome membrane breaks down.

A

cytoplasm

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16
Q

Mutations in genes that encode lysosomal degradative enzymes result in ___ ___ ___ - undegraded material accumulates in the lysosomes of affected individuals.

A

lysosomal storage diseases

17
Q

___ ___ is caused by deficiency of glucocerebrosidase, which catalyzes hydrolysis of glucosylceramide to glucose and ceramide.

A

Gaucher disease

18
Q

Gaucher disease is caused by deficiency of ___, which catalyzes hydrolysis of glucosylceramide to glucose and ceramide.

A

glucocerebrosidase

19
Q

Gaucher disease is caused by deficiency of glucocerebrosidase, which catalyzes hydrolysis of glucosylceramide to ___ and ___.

A

glucose, ceramide

20
Q

In the most common form of Gaucher disease, ___ are the only cells affected. Their function is to eliminate aged and damaged cells by phagocytosis

A

macrophages

21
Q

Lysosomes digest material taken up from outside the cell by ___.

A

endocytosis

22
Q

Lysosomes are formed when transport vesicles from the ___ ___ fuse with a late endosome.

A

Trans-Golgi Network

23
Q

___ represent an intersection between the secretory pathway and the endocytic pathway.

A

Endosomes

24
Q

___ types of endosomes.

A

3

25
Q

Three types of endosomes:

A

early endosomes, recycling endosomes, late endosomes

26
Q

___ ___ fuse with endocytic vesicles from the plasma membrane.
They separate molecules for recycling from molecules destined for degradation in lysosomes.

A

early endosomes

27
Q

Molecules to be recycled are passed to ___ ___ and back to the plasma membrane.

A

recycling endosomes

28
Q

Lysosomes degrade:

1) Cellular materials (proteins, organelles) by ___.
2) Extracellular materials taken up by ___.

A

autophagy, phagocytosis

29
Q

___ - Turnover of the cell’s own components.

Important in embryonic development and programmed cell death.

A

autophagy

30
Q

Autophagy:

A small area of cytoplasm or organelle is enclosed in a vesicle (___) which fuses with a lysosome, and its contents are digested.

A

autophagosome