Lecture 8: Protein folding disorders Flashcards
Improper degradation
Overactive cellular degradation systems (ERAD) can contribute to accumulation of mutant, misfolded, incomplete degraded proteins
Improper localization
Misfolded proteins lead to improper subcellular localization causing:
- loss of function
- gain of function toxicity
Mutant protein effect on WT protein
Mutant protein antagonizes the function of WT protein
- loss of protein activity
- interferes with function of WT protein at cellular and structural levels
Gain of toxic function
Protein conformational changes can cause dominant phenotypes
-APOE4 disrupts mitochondrial function, impairs neurite outgrowth
Src kinases in cancer
Amyloid fibers are what, and contain what sequence
Insoluble protein aggregates
VQIVY
How can amyloidogenic protein aggregates effect cells?
They can form pore-like structures, disrupting the membrane integrity
What enhances the formation of amyloid fibers
Covalent modifications
Potential remediation processes
Blocking the aggregate formation by:
- small molecules (chaperones) as stabilizer
- Site specific antibodies recognize conformational changes or specific sequences such as (VQIVY)
What are the keystones for environmental stressors
Detect
Adapt
Respond
What can increase life expectancy
Intrinsic induction of stress defense programs resulting in adaptation
Hormetic stress
Applying moderate levels of stress could trigger beneficial adaptive stress pathways, allowing longer life
Cellular and organismal functionality requires
Protein production
Folding
Degredation
Proteostasis pathway in Cytosol
HSR
Proteostasis pathway in ER
UPR(ER)
Proteostasis pathway in mitochondria
UPR(mt)
Membrane and secreted proteins fold and mature where
ER
What is the last line of defense for misfolded proteins
Apoptotic pathways
HSR
Heat shock response
Manages denatured proteins in the cytosol (HSF1)
Response to unfolded/misfolded proteins in ER
UPR-ER Increases protein chaperones Increase rate of ERAD Decrease protein production -Apoptosis is last resort
PQC proteases
Part of UPR in mitochondria
Specific to each mitochondrial compartment
Recognize and degrade misfolded proteins
Overload of quality control system
UPR mito can sense overload of QC system
-Activates transcription of nuclear encoded protective genes
Re-establish mitochondrial homeostasis