Translation elongation factor 2 is part of the target for a new family of antifungals

被引:55
作者
Capa, L [1 ]
Mendoza, A [1 ]
Lavandera, JL [1 ]
de las Heras, FG [1 ]
García-Bustos, JF [1 ]
机构
[1] Glaxo Wellcome SA, Dept Res, Tres Cantos 28760, Spain
基金
英国惠康基金;
关键词
D O I
10.1128/AAC.42.10.2694
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Translation elongation factor 2 (EF2), which in Saccharomyces cerevisiae is expressed from the EFT1 and EFT2 genes, has been found to he targeted by a new family of highly specific antifungal compounds derived from the natural product sordarin, Two complementation groups of mutants resistant to the semisynthetic sordarin derivative GM193663 were found. The major one (21 members) consisted of isolates with mutations on EFT2, The minor one (four isolates) is currently being characterized but it is already known that resistance in this group is not due to mutations on EFT1, pointing to the complex structure of the functional target for these compounds. Mutations on EF2 clustered, forming a possible drug binding Docket on a three-dimensional model of EF2, and mutant cell extracts lost the capacity to bind to the inhibitors. This new; family of antifungals holds the promise to be a much needed and potent addition to current antimicrobial treatments, as well as a useful tool for dissection of the elongation process in ribosomal protein synthesis.
引用
收藏
页码:2694 / 2699
页数:6
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