Unit 6 Flashcards

1
Q

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

Three Ways to Sort Proteins in Eukaryotic Cells

A

Protein sorting = transfer of proteins into compartments where they are needed
* synthesis of virtually all proteins starts in cytosol, on free ribosomes
* All protein transport requires energy
1. Transport through nuclear pores
2. Transport across membranes
3. Transport by vesicles

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3
Q

Signal Sequence

A
  • stretch of amino acids, at N-terminus, 15-60 amino acids 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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4
Q

Nuclear Pore Complex: highly selective gate

A
  • very high traffic through nuclear pores (500 molecules through each of the 3000-4000 per second) but flow is SELECTIVE
  • Proteins to be imported have nuclear localization sequence
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5
Q

Nuclear Pore Complexes — Gateways of the Nucleus

A
  • small molecules (even small proteins) freely pass through nuclear pores
  • Passage of larger proteins is active (energy-requiring) process
  • Nuclear localization signal - amino acid sequence that ‘tags’ a protein for import into the nucleus by nuclear transport
  • nuclear export signal tags a protein for export
  • Proteins pass through nuclear pore complexes without unfolding
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6
Q

What moves out of nucleus?

A
  • mature, properly processes mRNA
  • Ribosomal RNA (manufactured in nucleolus)
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7
Q

What moves into nucleus?

A
  • histones, proteins required for transcription and DNA replication
  • dNTPs, rNTPS
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8
Q

Transport across Membranes: Mitochondria

A
  • mitochondria and chloroplasts have a double membrane — chloroplasts have a third membrane (thylakoids)
  • although they have their own genomes and ribosomes, most of their proteins are encoded by nuclear genome so it must be imported
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9
Q

Transport across Membranes: Mitochondria pt 2

A
  • Proteins destined for mitochondria/chloroplasts made by free ribosomes in the cytosol
  • signal sequence at N terminus
  • proteins must be moved across both outer and inner
  • membranes at special sites where layers are in contact
  • proteins must unfold to be imported, then refold and signal sequence removed
  • Subsequent transport within organelle requires another signal sequence (exposed after first one removed)
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10
Q

Transport across Membranes: Endoplasmic Reticulum

A
  • ER is most extensive of Endomembrane system
  • Serves as an entry point for not only proteins for the ER itself, but rest of Endomembrane system (golgi, lysosomes, endosomes), cell surface, secretory proteins
  • Once in ER (in membrane or lumen), proteins will never re-enter cytosol
  • Synthesis of all proteins starts on free ribosomes
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11
Q

Two types of proteins transferred to ER:

A
  • water soluble proteins translocated completely across into ER lumen — destined for lumen of an organelle or secretion (out of cell)
  • Prospective transmembrane proteins translocated only partially across — destined for plasma membrane, ER membrane or membrane of another organelle
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12
Q

____ and ____ direct ribosome to ER

A

ER signal sequence and an SRP

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13
Q

Vesicular Transport

A

Temporary vesicles:
* 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

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14
Q

Vesicular Transport pt 2

A

with respect to proteins:
transport vesicles carry soluble proteins (in their lumens) and membrane proteins (in their membranes) between compartments

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15
Q

in general vesicle traffic is …

A
  • outward from ER: Golgi — other organelles? Plasma membrane?
  • Inward: plasma membrane — endosomes — lysosomes
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16
Q

Vesicle budding is driven by

A

formation of protein coat

17
Q

Clathrin-Coated Vesicles

A
  • mediate transport from outward face to golgi and inward from plasma membrane
  • Clathrin forms ‘basket’ that gives vesicle shape
  • ‘Adaptins’ capture specific cargo molecules by trapping the receptors that bind to them
18
Q

Outward Flow of Traffic within Endomembrane System

A

Rough ER: synthesis of proteins for - export (secretion) - insertion into membranes - lysosomesGolgi apparatus: collection, packaging & distribution

19
Q

Steps along the Secretory Pathway: ER Processing

A

most proteins are covalently modified in ER
1. formation of disulfide bonds
- stabilize protein shape
2. addition of sugar groups – glycosylation
various functions depending on protein …
- protect protein from degradation
- keep protein in ER until properly folded
- help direct to protein to proper organelle (act as transport signal for packaging into appropriate vesicles)
- if displayed on cell surface, cell-cell recognition

20
Q

Glycosylation in the ER

A

as growing peptide enters ER, ‘prefab’ carbohydrate group attaches to amino (NH2) groups of asparagine (Asn) side chains
“N-linked glycosylation”
Only properly folded proteins are allowed to leave ER

21
Q

“Unfolded Protein Response” (UPR)

A
  • if protein production 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
22
Q

Steps along the Secretory Pathway:Modification and Sorting in the Golgi Apparatus

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
23
Q

Functions of Golgi Apparatus: PTMs

A
  • 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 are synthesized in the golgi
  • Glycos amino glycans in extracellular matrix (animals)
  • Pectins, hemicellulose (plant cell walls)
24
Q

Vesicular Transport and Endocytic (Inward) Pathways

A
  • taking substances into cell by surrounding them with membrane
  • they become a membrane-bound vesicle
25
Q

2 main types of Vesicular Transport and Endocytic (Inward) Pathways, based on size of vesicles formed:

A
  • pinocytosis ‘cell drinking’ — tiny vesicles formed - endosomes
  • done only by eukaryotic cells
  • phagocytosis ‘cell eating’ — much larger vesicles - phagosomes
  • done only by specialized cell
26
Q

one more type of Vesicular Transport and Endocytic (Inward) Pathways in animal cells:

A
  • receptor-mediated endocytosis
  • very selective concentrating mechanisms
  • requires specialized receptors
27
Q

pinocytosis

A

“drinking”
* solutes, macromolecules, fluid
* ‘Bulk’ — any molecules present in enclosed fluid enter cell

28
Q

Phagocytosis

A

“eating”
* particles, other cells, debris

29
Q

receptor-mediated endocytosis

A
  • particular molecules (ligands) for which membrane has receptors
  • Receptors grouped in patches of membrane called coated pits
30
Q

site of cellular digestion

A

lysosomes