Inhibition of staphyloxanthin virulence factor biosynthesis in Staphylococcus aureus: In vitro, in vivo, and crystallographic results

Yongcheng Song, Chia I. Liu, Fu Yang Lin, Hwan No Joo, Mary Hensler, Yi Liang Liu, Wen Yih Jeng, Jennifer Low, George Y. Liu, Victor Nizet, Andrew H J Wang, Eric Oldfield

研究成果: 雜誌貢獻文章

62 引文 斯高帕斯(Scopus)

摘要

The gold color of Staphylococcus aureus is derived from the carotenoid staphyloxanthin, a virulence factor for the organism. Here, we report the synthesis and activity of a broad variety of staphyloxanthin biosynthesis inhibitors that inhibit the first committed step in its biosynthesis, condensation of two farnesyl diphosphate (FPP) molecules to dehydrosqualene, catalyzed by the enzyme dehydrosqualene synthase (CrtM). The most active compounds are phosphonoacetamides that have low nanomolar Ki values for CrtM inhibition and are active in whole bacterial cells and in mice, where they inhibit S. aureus disease progression. We also report the X-ray crystallographic structure of the most active compound, N-3-(3-phenoxyphenyl) propylphosphonoacetamide (IC50 = 8 nM, in cells), bound to CrtM. The structure exhibits a complex network of hydrogen bonds between the polar headgroup and the protein, while the 3-phenoxyphenyl side chain is located in a hydrophobic pocket previously reported to bind farnesyl thiodiphosphate (FsPP), as well as biphenyl phosphonosulfonate inhibitors. Given the good enzymatic, whole cell, and in vivo pharmacologic activities, these results should help guide the further development of novel antivirulence factor-based therapies for S. aureus infections.
原文英語
頁(從 - 到)3869-3880
頁數12
期刊Journal of Medicinal Chemistry
52
發行號13
DOIs
出版狀態已發佈 - 七月 9 2009
對外發佈Yes

ASJC Scopus subject areas

  • Molecular Medicine
  • Drug Discovery

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    Song, Y., Liu, C. I., Lin, F. Y., Joo, H. N., Hensler, M., Liu, Y. L., Jeng, W. Y., Low, J., Liu, G. Y., Nizet, V., Wang, A. H. J., & Oldfield, E. (2009). Inhibition of staphyloxanthin virulence factor biosynthesis in Staphylococcus aureus: In vitro, in vivo, and crystallographic results. Journal of Medicinal Chemistry, 52(13), 3869-3880. https://doi.org/10.1021/jm9001764