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DESCRIPTION (provided by applicant): The overall goal of this project is to identify potential drug targets and companion inhibitors that inhibit growth of Mycobacterium tuberculosis (Mtb), and other pathogenic bacteria in order to develop a foundation for antimicrobial drug discovery. We will accomplish this by identifying proteins that are targeted by whole cell growth inhibitors of Mtb discovered by a recently conducted high-throughput screen of over 200,000 drug-like small molecules. Proteins that are targets of inhibitors will be identified by genetic and complementary biochemical approaches. Structures will be determined, in collaboration with the Protein Structure Initiative Large-Scale Centers, of either the Mtb proteins that are targets of inhibitors or homologs of these proteins. In cases where a human homolog is available, that structure or that of a related eukaryotic protein will be determined as well. The structural information and inhibitor identities will be used along with annotations of related proteins to suggest molecular functions for each target protein. Assays for these molecular functions will be carried out to confirm both function and inhibition. Once targets are identified their inhibitors will additionally be analyzed for their activity against other pathogenic bacteria and eukaryotic cell lines. The targets will then be prioritized based on their novelty, the spectrum of activity of the companion growth inhibitor and the potency of the inhibitor. During the five years of the grant we expect to confirm the molecular targets for about 200 of the top whole cell active molecules and obtain the structures of these target proteins or members of the same sequence family. These structures, inhibitor-protein pairs, and biochemical information about the proteins will provide a rich resource of lead compounds and biochemistry for Mtb drug discovery, a foundation for understanding Mtb biology, and a path forward in the effort to improve human health by curing tuberculosis.
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Core B. Biochemistry and Enzymology
  • 批准号:
    10641863
  • 项目类别:
  • 资助金额:
    $13.56万
  • 财政年份:
    2020
  • 负责人:
    JAMES C SACCHETTINI
  • 依托单位:
Core B. Biochemistry and Enzymology
  • 批准号:
    10426177
  • 项目类别:
  • 资助金额:
    $13.24万
  • 财政年份:
    2020
  • 负责人:
    JAMES C SACCHETTINI
  • 依托单位:
Core B. Biochemistry and Enzymology
  • 批准号:
    10190811
  • 项目类别:
  • 资助金额:
    $12.93万
  • 财政年份:
    2020
  • 负责人:
    JAMES C SACCHETTINI
  • 依托单位:
Structure-based Discovery of Critical Vulnerabilities of Micobacteria
  • 批准号:
    8711232
  • 项目类别:
  • 资助金额:
    $191.51万
  • 财政年份:
    2012
  • 负责人:
    JAMES C SACCHETTINI
  • 依托单位:
国内基金
海外基金
Segmented Filamentous Bacteria激活宿主免疫系统抑制其拮抗菌 Enterobacteriaceae维持菌群平衡及其机制研究
  • 批准号:
    81971557
  • 项目类别:
    面上项目
  • 资助金额:
    65.0万元
  • 批准年份:
    2019
  • 负责人:
    毛开睿
  • 依托单位:
电缆细菌(Cable bacteria)对水体沉积物有机污染的响应与调控机制