High-throughput disulfide and FRET scanning to reveal protein conformational ensembles in vitro and in vivo.

Information

  • Research Project
  • 10191303
  • ApplicationId
    10191303
  • Core Project Number
    K99GM141459
  • Full Project Number
    1K99GM141459-01
  • Serial Number
    141459
  • FOA Number
    PA-20-188
  • Sub Project Id
  • Project Start Date
    9/10/2021 - 3 years ago
  • Project End Date
    8/31/2023 - a year ago
  • Program Officer Name
    FLICKER, PAULA F
  • Budget Start Date
    9/10/2021 - 3 years ago
  • Budget End Date
    8/31/2022 - 2 years ago
  • Fiscal Year
    2021
  • Support Year
    01
  • Suffix
  • Award Notice Date
    9/8/2021 - 3 years ago
Organizations

High-throughput disulfide and FRET scanning to reveal protein conformational ensembles in vitro and in vivo.

PROJECT SUMMARY Research Strategy Two of the biggest challenges in molecular biomedical research are (1) the lack of technologies for detailed investigation of protein conformations in the cell or the native environment, and (2) a dearth of data on protein conformational dynamics for large proteins and across time scales. This proposal addresses both these grand challenges head-on by developing two closely related technologies: high-throughput disulfide scanning, which will bridge the gap between in vitro and in vivo structural biology by revealing protein structures in both contexts, and single-molecule FRET scanning, which will reveal both average conformation and pairwise distance fluctuations across thousands of residue pairs within a protein in a massively parallel format. I will not only develop these powerful techniques, but also apply them to key biomedical questions: the role of conformational plasticity in the function of chaperones; the role of conformational dynamics in antibiotic susceptibility of bacterial transpeptidases; phenotypic effects of kinetically trapped and non-native protein conformations; and structural basis of genotype-phenotype relationships. Candidate and Environment I am a highly trained experimental protein biochemist and biophysicist with extensive experience investigating the roles of disulfide bonds and redox chemistry in protein structure, stability, misfolding, aggregation, and the pathogenesis of disease. By carrying out the proposed research, I will acquire crucial technical expertise in emerging protein sequencing technologies and computational modeling and data analysis algorithms, as well as a deeper knowledge of statistical physics, microbial physiology, and experimental evolution. Harvard University and the greater Boston-area academic community provides a stellar environment for academic professional development. A group of world-leading experts has been recruited as the Advisory Committee. The primary mentor has a proven track record of training future faculty members at top research-intensive institutions. I will take full advantage of career-development courses, workshops on inclusive teaching and building communities of belonging, seminars on leading a research group, guidance and practice in mentorship, and a formal refresher on responsible conduct of research. I have maintained a high level of productivity throughout my research career (14 publications in 8 years, starting as an undergraduate), and the work arising from this award will be widely disseminated and shared.

IC Name
NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES
  • Activity
    K99
  • Administering IC
    GM
  • Application Type
    1
  • Direct Cost Amount
    92592
  • Indirect Cost Amount
    7407
  • Total Cost
    99999
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    859
  • Ed Inst. Type
    SCHOOLS OF ARTS AND SCIENCES
  • Funding ICs
    NIGMS:99999\
  • Funding Mechanism
    OTHER RESEARCH-RELATED
  • Study Section
    ZGM1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    HARVARD UNIVERSITY
  • Organization Department
    CHEMISTRY
  • Organization DUNS
    082359691
  • Organization City
    CAMBRIDGE
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    021385319
  • Organization District
    UNITED STATES