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Grant: Project Grant

University of Calgary

$849,150.00

Integrative Structural Modeling of a Master End-Sensing Synapse in DNA Double Strand Break Repair

EF 2020-21

Résumé
The cellular DNA damage repair response protects us from genotoxins and maintains the stability of our genome. When errors accumulate in the repair machinery, we are prone to both cancer and age-associated diseases. A functioning response is essential even for cancer cells, so a standard therapeutic approach is to overwhelm the repair response using "blunt instruments" such as ionizing radiation and genotoxic drugs. This level of targeting is crude by any measure, leading to unwanted toxicities and an incomplete response. The applied goal of our project is to better understand how mechanisms of DNA repair work, in order to sensitize cancer cells to existing therapies. While DNA damage takes many forms, Double Strand Breaks (DSBs) are particularly dangerous and their repair machinery is a compelling target for anticancer therapy. The response to a DSB involves interacting mechanisms that generate different repair outcomes. Our proposal seeks to establish the structural and functional properties of a master end-sensing complex that ultimately determines how the repair program unfolds. The key protein involved in this end-sensing complex is a massive kinase called DNA-PKcs. One of our major goals is to determine how this protein responds to the damage event itself, not just the signalling events that initiate them. They must work together to determine repair outcomes. To do this, we will use cutting-edge structural techniques, including Cryo-Electron Microscopy, Hydrogen-Deuterium Exchange Mass Spectrometry and Crosslinking Mass Spectrometry. We have assembled an excellent team of collaborators to assist in translating molecular/structural insights into mechanistic validations at the cellular level, in order to define new strategies for targeting cancer.
Programme
Project Grant
Bénéficiaire
Emplacement
Alberta, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
433659
Name
Schriemer David C
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Cancer Research
Theme2
Biomedical
Prcname2
Biochemistry & Molecular Biology - A
Projecttitle
Integrative Structural Modeling of a Master End-Sensing Synapse in DNA Double Strand Break Repair
Programtype2
Operating Grants
Orgnameinp2
University of Calgary
Cihramount2
$849,150
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Crosslinking Mass Spectrometry; Dna Damage Signalling; Dna Repair; Electron Microscopy; Homologous Repair Recombination; Hydrogen Deuterium Exchange Mass Spectrometry; Non-Homologous End Joining; Protein Complexes; Protein-Dna Interactions
Abstract
The cellular DNA damage repair response protects us from genotoxins and maintains the stability of our genome. When errors accumulate in the repair machinery, we are prone to both cancer and age-associated diseases. A functioning response is essential even for cancer cells, so a standard therapeutic approach is to overwhelm the repair response using "blunt instruments" such as ionizing radiation and genotoxic drugs. This level of targeting is crude by any measure, leading to unwanted toxicities and an incomplete response. The applied goal of our project is to better understand how mechanisms of DNA repair work, in order to sensitize cancer cells to existing therapies. While DNA damage takes many forms, Double Strand Breaks (DSBs) are particularly dangerous and their repair machinery is a compelling target for anticancer therapy. The response to a DSB involves interacting mechanisms that generate different repair outcomes. Our proposal seeks to establish the structural and functional properties of a master end-sensing complex that ultimately determines how the repair program unfolds. The key protein involved in this end-sensing complex is a massive kinase called DNA-PKcs. One of our major goals is to determine how this protein responds to the damage event itself, not just the signalling events that initiate them. They must work together to determine repair outcomes. To do this, we will use cutting-edge structural techniques, including Cryo-Electron Microscopy, Hydrogen-Deuterium Exchange Mass Spectrometry and Crosslinking Mass Spectrometry. We have assembled an excellent team of collaborators to assist in translating molecular/structural insights into mechanistic validations at the cellular level, in order to define new strategies for targeting cancer.
Competitiondate
202010
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Schriemer, David C
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $849,150~ $0~
University of Calgary - $849,150 Grant (2020-21) | Canada Spends