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Grant: Operating Grant

University of Toronto

$544,759.00

Biology and pathobiology of alpha-synuclein

FY 2012-13

Summary
Alpha-Synuclein (alpha-syn) is a major protein in neurons that is implicated in Parkinson disease (PD). We have identified high molecular weight protein complexes that contain alpha-syn in rodents and human brains and have identified some components of these complexes. Because these complexes represent an important link to the pathological alpha-syn aggregates that build up in PD brains, it is essential that we investigate the intermediary biochemical changes that cause them to become impaired and dysfunctional. Recent studies also implicate the transfer of misfolded alpha-syn from one neuron to another as a major culprit in the spread of PD pathology such as Lewy bodies. It is possible that oxidative stress and dysfunctional protein breakdown pathways alter the balance of alpha-syn binding partners causing premature disassembly or accumulation of aberrant and toxic complexes, which can then be transferred to adjacent neurons and propagate the neurotoxicity. Therefore we will develop a novel system to measure the neuron-to-neuron movement of alpha-syn and also test whether aggregated alpha-syn can be used to seed pathology in otherwise healthy tissue.
Program
Operating Grant
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
278541
Name
Tandon Anurag
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Aging
Theme2
Biomedical
Prcname2
Cell Biology & Mechanisms of Disease
Projecttitle
Biology and pathobiology of alpha-synuclein
Programtype2
Operating Grants
Orgnameinp2
University of Toronto
Cihramount2
$544,759
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Brain; Lewy Bodies; Neurodegeneration; Neurons; Parkinson Disease; Prion; Protein Aggregation; Protein Degradation; Protein Secretion; Protein Uptake
Abstract
Alpha-Synuclein (alpha-syn) is a major protein in neurons that is implicated in Parkinson disease (PD). We have identified high molecular weight protein complexes that contain alpha-syn in rodents and human brains and have identified some components of these complexes. Because these complexes represent an important link to the pathological alpha-syn aggregates that build up in PD brains, it is essential that we investigate the intermediary biochemical changes that cause them to become impaired and dysfunctional. Recent studies also implicate the transfer of misfolded alpha-syn from one neuron to another as a major culprit in the spread of PD pathology such as Lewy bodies. It is possible that oxidative stress and dysfunctional protein breakdown pathways alter the balance of alpha-syn binding partners causing premature disassembly or accumulation of aberrant and toxic complexes, which can then be transferred to adjacent neurons and propagate the neurotoxicity. Therefore we will develop a novel system to measure the neuron-to-neuron movement of alpha-syn and also test whether aggregated alpha-syn can be used to seed pathology in otherwise healthy tissue.
Competitiondate
201303
Approvedterm2
4 yrs 0 mth
Pinamesdelim
Tandon, Anurag
Approvedterm
4 ans 0 mois
Cihrcontribution2
~ $544,759~ $0~
University of Toronto - $544,759 Grant (2012-13) | Canada Spends