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Active TRAINING, INDIVIDUAL NIH (US)

Harnessing Redox Regulation of Proteasome Function to Promote Healthy Aging

$797.6K USD

Funder NATIONAL INSTITUTE ON AGING
Recipient Organization Harvard School of Public Health
Country United States
Start Date Aug 09, 2024
End Date Aug 08, 2027
Duration 1,094 days
Number of Grantees 1
Roles Principal Investigator
Data Source NIH (US)
Grant ID 10983419
Grant Description

PROJECT SUMMARY For half a century, groups across the world have been investigating the hypothesis that reactive oxygen species influence the biology of aging. However, technical limitations have, until recently, heavily limited the precision at which studies can interrogate this hypothesis. For example, reactive oxygen species are

known to post-translationally modify cysteine residues on proteins throughout the proteome, however, only recently have proteomic techniques been developed allowing for deep and quantitative analysis of cysteine oxidation on proteins in a biological sample. This proposal will develop preliminary data which

identified a broad increase in cysteine oxidation across 10,970 cysteines in the proteome in C. elegans during aging and begin to link these events to regulation of the biology of aging. Specifically, this proposal will focus on redox regulation of proteasome activity during aging. First, this proposal will determine the relative

contribution of cysteine oxidation to regulating age-dependent changes to proteasome activity. Second, this proposal will identify and define regulatory cysteines involved in redox regulation of the proteasome and determine their influence in the maintenance of longevity. Third, this proposal will generate new cysteine

oxidation data sets to determine how longevity interventions influence the trajectory of age-dependent cysteine oxidation. Finally, this proposal will evaluate the intriguing hypothesis that reactive oxygen species can be carefully titrated to promote fitness through stimulating dormant proteasome activity in

aged organisms. This work will synergistically employ the skillsets of multiple investigators to perform impactful, cutting-edge research. In addition to providing significant insights into important areas of cell biology, the proposed work will also contribute to the development of a future academic scientist at Harvard’s

T.H. Chan School of Public Health, one of the best places to receive scientific training in the world. These studies will both develop a research program which the trainee can use to establish an independent, academic scientific research group as well as equip the trainee with the skillset needed to be successful in this

professional domain. The trainee will receive experience in all areas required of a successful academic investigator, such as mentoring, scientific communication, grant writing, project management and budgeting and receive significant technical training in a new model system, new fields and many new

techniques. Together, this work will define fundamental mechanisms contributing to development of the biology of aging with broad implications for human health and disease and provide strategies to promote healthy aging.

All Grantees

Harvard School of Public Health

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