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  • 标题:Blueprint for antimicrobial hit discovery targeting metabolic networks
  • 本地全文:下载
  • 作者:Y. Shen ; J. Liu ; G. Estiu
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:2010
  • 卷号:107
  • 期号:3
  • 页码:1082-1087
  • DOI:10.1073/pnas.0909181107
  • 语种:English
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:Advances in genome analysis, network biology, and computational chemistry have the potential to revolutionize drug discovery by combining system-level identification of drug targets with the atomistic modeling of small molecules capable of modulating their activity. To demonstrate the effectiveness of such a discovery pipeline, we deduced common antibiotic targets in Escherichia coli and Staphylococcus aureus by identifying shared tissue-specific or uniformly essential metabolic reactions in their metabolic networks. We then predicted through virtual screening dozens of potential inhibitors for several enzymes of these reactions and showed experimentally that a subset of these inhibited both enzyme activities in vitro and bacterial cell viability. This blueprint is applicable for any sequenced organism with high-quality metabolic reconstruction and suggests a general strategy for strain-specific antiinfective therapy.
  • 关键词:antibiotics ; flux balance analysis ; virtual screening
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