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DESCRIPTION (provided by applicant): The majority of pharmaceuticals are derived from natural products either directly or indirectly. However, the pipeline to new natural products has been drying up over the last decades as the technologies became less amenable to high- throughput screening and as finding new natural products became increasingly difficult. Substantial progress has been made in these areas by numerous labs, but there are still gaps in technology and in basic understanding of natural product sources. In this project, we will provide new methods and data to help fill these remaining gaps. In addition, we will build natural product compound libraries for screening at NIH and at the University of Wisconsin. The new methods include more rapid, automated, and integrated techniques for extraction, purification, and dereplication of natural products. Basic studies of natural product sources using marine symbiotic bacteria are aimed at answering questions about the most fruitful places to find new natural product producers and about methods to obtain these promising bacteria. These biological and chemical studies are synergistic and will provide the first large, ordered set of data linking cultivated symbiotic bacteria to chemistry in whole animals. The resulting methods are designed to be widely useful in multiple labs and to help in the development of broadly shared platforms for dereplication. The resulting libraries of natural products will be used in a variety of screens at established, high-throughput centers at NIH and U. Wisconsin. We will pursue promising leads as potential new pharmaceuticals. PUBLIC HEALTH RELEVANCE: We will develop new methods for the rapid discovery of bioactive natural products and provide new data about sources of natural products that enable drug discovery. We will also provide libraries of natural products for screening. These results will have a large impact on natural products sciences because of new methods and knowledge. The human health impact will result from these new methods and potentially from new therapeutic small molecules discovered in the course of the project.
期刊论文(7)
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会议论文
Bacterial endosymbiosis in a chordate host: long-term co-evolution and conservation of secondary metabolism.
脊全宿主中的细菌性内生物无生物:长期共同进化和继发代谢。
DOI: 10.1371/journal.pone.0080822
发表时间: 2013
期刊: PloS one
影响因子: 3.7
作者: [Kwan JC, Schmidt EW]
通讯作者: Schmidt EW
Structure elucidation of uniformly 13C labeled small molecule natural products.
统一 13C 标记的小分子天然产物的结构解析。
DOI: 10.1002/mrc.4384
发表时间: 2015
期刊: Magnetic resonance in chemistry : MRC
影响因子: --
作者: [Reibarkh,Mikhail, Wyche,ThomasP, Saurí,Josep, Bugni,TimS, Martin,GaryE, Williamson,RThomas]
通讯作者: Williamson,RThomas
DOI: 10.1021/np300034c
发表时间: 2012-04-27
期刊: Journal of natural products
影响因子: 5.1
作者: [Adnani N, Michel CR, Bugni TS]
通讯作者: Bugni TS
Host control of symbiont natural product chemistry in cryptic populations of the tunicate Lissoclinum patella.
被囊动物 Lissoclinum patella 隐秘种群中共生天然产物化学的宿主控制。
DOI: 10.1371/journal.pone.0095850
发表时间: 2014
期刊: PloS one
影响因子: 3.7
作者: [Kwan,JasonC, Tianero,MaDiareyB, Donia,MohamedS, Wyche,ThomasP, Bugni,TimS, Schmidt,EricW]
通讯作者: Schmidt,EricW
Symbiosis and Chemical Diversity Generation
  • 批准号:
    10552461
  • 项目类别:
  • 资助金额:
    $53.96万
  • 财政年份:
    2023
  • 负责人:
    Eric W Schmidt
  • 依托单位:
Modulating single cell types in the sensory nervous system
  • 批准号:
    10522412
  • 项目类别:
  • 资助金额:
    $54.21万
  • 财政年份:
    2022
  • 负责人:
    Eric W Schmidt
  • 依托单位:
Microbial Ecology-Guided Discovery of Antibacterial Drugs
  • 批准号:
    10446908
  • 项目类别:
  • 资助金额:
    $66.48万
  • 财政年份:
    2022
  • 负责人:
    Eric W Schmidt
  • 依托单位:
Modulating single cell types in the sensory nervous system
  • 批准号:
    10641952
  • 项目类别:
  • 资助金额:
    $54.21万
  • 财政年份:
    2022
  • 负责人:
    Eric W Schmidt
  • 依托单位:
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