Lecture 8: Protein folding disorders Flashcards

1
Q

Improper degradation

A

Overactive cellular degradation systems (ERAD) can contribute to accumulation of mutant, misfolded, incomplete degraded proteins

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2
Q

Improper localization

A

Misfolded proteins lead to improper subcellular localization causing:

  • loss of function
  • gain of function toxicity
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3
Q

Mutant protein effect on WT protein

A

Mutant protein antagonizes the function of WT protein

  • loss of protein activity
  • interferes with function of WT protein at cellular and structural levels
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4
Q

Gain of toxic function

A

Protein conformational changes can cause dominant phenotypes
-APOE4 disrupts mitochondrial function, impairs neurite outgrowth
Src kinases in cancer

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5
Q

Amyloid fibers are what, and contain what sequence

A

Insoluble protein aggregates

VQIVY

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6
Q

How can amyloidogenic protein aggregates effect cells?

A

They can form pore-like structures, disrupting the membrane integrity

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7
Q

What enhances the formation of amyloid fibers

A

Covalent modifications

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8
Q

Potential remediation processes

A

Blocking the aggregate formation by:

  • small molecules (chaperones) as stabilizer
  • Site specific antibodies recognize conformational changes or specific sequences such as (VQIVY)
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9
Q

What are the keystones for environmental stressors

A

Detect
Adapt
Respond

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10
Q

What can increase life expectancy

A

Intrinsic induction of stress defense programs resulting in adaptation

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11
Q

Hormetic stress

A

Applying moderate levels of stress could trigger beneficial adaptive stress pathways, allowing longer life

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12
Q

Cellular and organismal functionality requires

A

Protein production
Folding
Degredation

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13
Q

Proteostasis pathway in Cytosol

A

HSR

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14
Q

Proteostasis pathway in ER

A

UPR(ER)

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15
Q

Proteostasis pathway in mitochondria

A

UPR(mt)

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16
Q

Membrane and secreted proteins fold and mature where

A

ER

17
Q

What is the last line of defense for misfolded proteins

A

Apoptotic pathways

18
Q

HSR

A

Heat shock response

Manages denatured proteins in the cytosol (HSF1)

19
Q

Response to unfolded/misfolded proteins in ER

A
UPR-ER
Increases protein chaperones
Increase rate of ERAD
Decrease protein production
-Apoptosis is last resort
20
Q

PQC proteases

A

Part of UPR in mitochondria
Specific to each mitochondrial compartment
Recognize and degrade misfolded proteins

21
Q

Overload of quality control system

A

UPR mito can sense overload of QC system
-Activates transcription of nuclear encoded protective genes
Re-establish mitochondrial homeostasis