Lecture 20 Transmembrane proteins, Golgi, COP Flashcards

1
Q

A protein targeted to the ER lumen, after it
is fully synthesized and properly folded,
has 1 of 2 options

A

Option 1. It is retained in the ER lumen, if
that is where it functions

Option 2. It is transported from the ER to the Golgi complex for further modification and delivered to distal parts of the biosynthetic/secretory pathway (e.g. Golgi, lysosomes, plasma membrane). In some cases, the final destination could be outside the cell

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2
Q

The Golgi apparatus receives proteins and lipids from….

A

the ER and sorts them to other organelles, the plasma membrane or the cell exterior

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3
Q

Material moves from ER to…

A

Golgi and then to other
compartments and the
plasma membrane in a
proximal to distal direction

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4
Q

what does TGN and CGN stand

A

trans-Golgi
network, cis-Golgi
network

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5
Q

what is the Structure of Golgi Complex?

A
  • Smooth, flattened, disk-like cisterna (~0.5-1 micron in diameter).
  • ~8 (or fewer) cisternae/stack—range
    from a few to several 1000 stacks per cell.
  • Curved like a shallow bowl.
  • Shows polarity: cis medial–trans cisternae.
  • Cisternae are biochemically unique.
  • Membrane supported by protein skeleton (actin, spectrin).
  • Scaffold linked to motor proteins that direct movement of vesicles
    into and out of the Golgi.
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6
Q

CGN acts as a what

A

sorting station (i.e.,
sorts whether proteins should continue
on to the next Golgi station or be shipped back to the ER)

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7
Q

TGN sorts protein into different types of what

A

vesicles—vesicles go to plasma
membrane or other intracellular
destinations (e.g. lysosomes)

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8
Q

Golgi is the ______ ______of the cell

A

processing plant

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9
Q

In addition to sorting, the Golgi is also involved in synthesis of ________ and
specific ________ of proteins and lipids (glycosylation and proteolytic modification)

A

polysaccharides, modification

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10
Q

Different cisternae of the Golgi contain

A

different enzymes that modify proteins

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11
Q

Proteins are modified _____-_____ as they traverse the Golgi; fully processed _______
at the TGN

A

step-wise, proteins

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12
Q

the differential staining of the Golgi cisternae reflects their…

A

biochemical differences

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13
Q

Fully processed proteins are sorted to the…

A

trans-Golgi network (TGN), and then sorted and delivered to their final
destinations

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14
Q

Exocytosis:
Mucin secretion is
an example of

A

constitutive
secretory pathway

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15
Q

the release of
insulin and
neurotransmitters
is what pathway?

A

regulated secretory pathway

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16
Q

Defective protein targeting and trafficking causes many diseases through what mechanisms? (2)

A

Protein truncations / Single-nucleotide polymorphisms (SNPs)

17
Q

Cystic fibrosis (CF) is caused by a mutation what gene

A

in the cystic fibrosis transmembrane conductance regulator
(CFTR) gene

18
Q

name and describe the most common mutation

A

ΔF508, is
a deletion of three nucleotides that results in a loss of the amino acid phenylalanine (F) at the 508th position of the protein. This mutation accounts for two-thirds (66–70%) of CF cases worldwide.

19
Q

where are Fully processed proteins sorted to

A

the trans-Golgi network (TGN) then to final destinations

20
Q

The transfer of vesicles from ER to
Golgi, and between the Golgi sub-compartments, is achieved by…

A

coat proteins

21
Q

Coat proteins have 2 functions:

A
  1. Helps form the vesicle.
  2. Helps select ‘cargo’ (i.e. material inside or on vesicle)
22
Q

Electron micrographs reveal what on vesicles

A

dense protein coat (COPI and COPII)

23
Q

what are COPI and COPII

A

protein complexes that assemble on the
cytosolic surface of donor compartment membranes at sites where
budding takes place

24
Q

what protein complex does this describe?

coated vesicles move in
retrograde direction

A

COPI

25
Q

what protein complex does this describe?

coated vesicles move in
anterograde direction

A

COPII

26
Q

Lysosomes: Key Features

A
  • Digestive organelles
  • Size: 25 nm to 1 μm
  • Internal pH of 4.6 (proton
    pump or H+-ATPase)
  • Contains hydrolytic enzymes: acid hydrolases
  • Lysosomal membrane is
    composed of glycosylated
    proteins that act as a protective lining next to acidic lumen