Unit 5:Intercellular Compartments and Protein Sorting Flashcards

1
Q

What is the evolution of internal membranes of eukaryotes?

A

precursors of eukaryotes believed to be organisms (like bacteria) with no internal membranes
plasma membrane carried out all membrane-related functions
endomembrane system thought to have evolved as invagination of plasma membrane
mitochondria and chloroplasts thought to have evolved as endosymbionts

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2
Q

Why is the cytoskeleton important?

A

-cell shape
-cell motility
-movement / position of organelles
-movement of materials within cell
-movement of chromosomes during mitosis

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3
Q

What does protein sorting mean?

A

-the transfer of proteins into compartments where they are needed

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4
Q

Where does the synthesis of all proteins start?

A

-in the cytosol on free ribosomes

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5
Q

Does protein transport require energy?

A

Yes

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6
Q

What directs proteins to the right place?

A

-stretch of amino acids, located at N-terminus, 15-60 AAs long, that directs proteins to particular organelles
-signal sequences for nucleus, mito/chloro, peroxisomes or ER
-usually removed after sorting

-delete or transfer sequence to another protein=protein goes to wrong ‘address’

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7
Q

Can small molecules freely pass through nuclear pores?

A

Yes

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8
Q

Can large proteins pass though nuclear pores?

A

No, the passage of large proteins is active
proteins pass through nuclear pores without unfolding

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9
Q

What is the nuclear localization signal?

A
  • amino acid sequence that ‘tags’ a protein for import into the nucleus by nuclear transport
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10
Q

what does the nuclear export signal do?

A

tags a protein for export

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11
Q

What moves out of the nucleus?

A

mature, properly processed mRNA
assembled ribosomal subunits (rRNA)

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12
Q

What moves into the nucleus?

A

histones, ribosomal proteins, proteins required for transcription & DNA replication
dNTPs, rNTPs

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13
Q

What are modifications done by the ER?

A

-formation of disulfide bonds
-stabilization
-addition of sugar groups
-protect
-keep in ER
-direct
-cell-cell recognition

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14
Q

What happens if protein production exceeds capacity?

A

if protein prod’n exceeds capacity to keep up with folding
- misfolded proteins accumulate
-signals lead to increased expression of chaperone proteins and other proteins that assist in folding, expansion of the ER …
-if cell still can’t keep up, UPR will trigger cell death= apoptosis

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15
Q

What do transport vesicles do with proteins?

A

-transport vesicles carry soluble proteins (in their lumens) and membrane proteins (in their membranes) between compartments

in general vesicle traffic is …
outward from ER =>Golgi =>other organelles? plasma membrane?
-inward, from plasma membrane => lysosomes

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16
Q

What happens in the Golgi apparatus in the secretory pathway of protein?

A

series of flattened sacs – cisternae
organized into functionally distinct compartments with cis (entry) face closest to ER, trans (exit) face at other end
cis – newly formed
trans – breaking away
modification of new proteins arriving from ER:
peptide chains shortened by proteases
amino acids modified
CHO groups that were added in ER modified or removed
glycosylation
different CHO groups added to different AAs (ser, thr)
“O-linked glycosylation”

most complex polysaccharides synthesized in Golgi
glycos amino glycans in extracellular matrix (animals)
pectins, hemicellulose (plant cell walls)

17
Q

Constitutive secretion

A

-constant recreation
-unregulated

18
Q

What happens to the plasma membrane during secretion?

A

The plasma membrane gets bigger

19
Q

What happens in the endocytic Process(inward)

A

taking substances into cell by surrounding them with membrane
they become a membrane-bound vesicle
2 main types, based on size of vesicles formed:
pinocytosis ‘cell drinking’ – tiny vesicles formed - endosomes
done by all eukaryotic cells
phagocytosis ‘cell eating’ – much larger vesicles – phagosomes
only done by specialized cells

one more type in animal cells:
receptor-mediated endocytosis
very selective concentrating mechanisms
requires specialized receptors

20
Q

What is pinocytosis?

A

pinocytosis “drinking”
solutes, macromolecules, fluid
‘bulk’ – any molecules present in enclosed fluid enter cell

21
Q

What is phagocytosis?

A

phagocytosis “eating”
particles, other cells, debris

22
Q

What is receptor-mediated endocytosis?

A

-particular molecules (ligands) for which membrane has receptors
receptors grouped in patches of membrane called coated pits

23
Q

If a protein does not have a location signal where does it end up?

A

cytosol

24
Q

Where do all proteins start synthesis?

A

cytosol by free ribosomes

25
Q

What happens to the membrane associated with a vesicle that has exocytosed by its cargo?

A

the vesticle membrane fuses with the plasma membrane and becomes part of it

26
Q

How many membranes does the mitochondria have?

A

2

27
Q

How many membranes does a chloroplast have?

A

three

28
Q

What happens when a protein is needed in the chloroplast or mitochondria

A

-signal sequence at N terminus
-proteins must be moved across both outer and inner membranes at special sites where layers are in contact

29
Q

What steps are involved in protein import?

A

-proteins must be unfolded to be imported
-upon import must be folded and have the signal sequence removed

30
Q

What are the two types of proteins transferred to the ER?

A

-water soluble proteins translocated completely across into ER lumen
-destined for secretion, or lumen of an organelle
-prospective transmembrane proteins translocated only partially across
-destined for plasma membrane, ER membrane or membrane of another organelle

31
Q

What do temporary vesicles do?

A

-allow material to leave and enter cells
-move material between endomembrane compartments
-carry soluble proteins (in their lumens) to the plasma membrane for secretion
-move membrane proteins (in their membranes) to be expressed on the cell surface