Systems-level metabolic flux profiling identifies fatty acid synthesis as a target for antiviral therapy

被引:0
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作者
Joshua Munger
Bryson D Bennett
Anuraag Parikh
Xiao-Jiang Feng
Jessica McArdle
Herschel A Rabitz
Thomas Shenk
Joshua D Rabinowitz
机构
[1] Lewis Thomas Laboratory,Department of Molecular Biology
[2] Princeton University,Department of Biochemistry and Biophysics
[3] University of Rochester School of Medicine and Dentistry,Department of Chemistry and Lewis
[4] 601 Elmwood Ave,Sigler Institute for Integrative Genomics
[5] Box 712,Department of Chemistry
[6] Rochester,undefined
[7] New York 14642,undefined
[8] USA,undefined
[9] Carl Icahn Laboratory,undefined
[10] Princeton University,undefined
[11] Frick Laboratory,undefined
[12] Princeton University,undefined
来源
Nature Biotechnology | 2008年 / 26卷
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摘要
Munger et al. show that infection with human cytomegalovirus upregulates fatty acid biosynthesis and that pharmacological inhibition of this pathway inhibits replication of both this virus and influenza A. This approach, the first to reliably map major carbon fluxes in mammalian cells, extends the promise of metabolomics from diagnostic applications to identification of new therapeutic concepts.
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页码:1179 / 1186
页数:7
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