Mapping Interactions of Microbial Metabolites with Human G-Protein-Coupled Receptors

被引:128
作者
Colosimo, Dominic A. [1 ]
Kohn, Jeffrey A. [1 ]
Luo, Peter M. [1 ]
Piscotta, Frank J. [1 ]
Han, Sun M. [3 ]
Pickard, Amanda J. [2 ]
Rao, Arka [2 ]
Cross, Justin R. [2 ]
Cohen, Louis J. [3 ]
Brady, Sean F. [1 ]
机构
[1] Rockefeller Univ, Lab Genetically Encoded Small Mol, 1230 York Ave, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Donald B & Catherine C Marron Canc Metab Ctr, New York, NY 10065 USA
[3] Icahn Sch Med Mt Sinai, Dept Med, Div Gastroenterol, New York, NY 10029 USA
基金
美国国家卫生研究院;
关键词
BRAIN ANGIOGENESIS INHIBITOR-1; GUT MICROBIOTA; NEUROMEDIN-U; ACID; FATTY; IDENTIFICATION; BIOSYNTHESIS; FERMENTATION; RECOGNITION; ENGULFMENT;
D O I
10.1016/j.chom.2019.07.002
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Despite evidence linking the human microbiome to health and disease, how the microbiota affects human physiology remains largely unknown. Microbiota-encoded metabolites are expected to play an integral role in human health. Therefore, assigning function to these metabolites is critical to understanding these complex interactions and developing microbiota-inspired therapies. Here, we use large-scale functional screening of molecules produced by individual members of a simplified human microbiota to identify bacterial metabolites that agonize G-protein-coupled receptors (GPCRs). Multiple metabolites, including phenylpropanoic acid, cadaverine, 9-10-methylenehexadecanoic acid, and 12-methyltetradecanoic acid, were found to interact with GPCRs associated with diverse functions within the nervous and immune systems, among others. Collectively, these metabolite-receptor pairs indicate that diverse aspects of human health are potentially modulated by structurally simple metabolites arising from primary bacterial metabolism.
引用
收藏
页码:273 / +
页数:17
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