Drugs targeting the ribosome

被引:140
作者
Hermann, T [1 ]
机构
[1] Anadys Pharmaceut Inc, Dept Struct Chem, San Diego, CA 92121 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.sbi.2005.05.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Several classes of clinically important antibiotics target the bacterial ribosome, where they interfere with microbial protein synthesis. Structural studies of the interaction of antibiotics with the ribosome have revealed that these small molecules recognize predominantly the rRNA components. Over the past two years, three-dimensional structures of ribosome-anti biotic complexes have been determined, providing a detailed picture of the binding sites and mechanism of action of antibacterials, including 'blockbuster' drugs such as the macrolicles. Structure-based approaches have come to fruition that comprise the design and crystal structure analysis of novel semi-synthetic antibiotics that target the ribosome decoding site.
引用
收藏
页码:355 / 366
页数:12
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