The A-Z of bacterial translation inhibitors

被引:254
作者
Wilson, Daniel N. [1 ,2 ,3 ]
机构
[1] Univ Munich, LMU, Gene Ctr, D-81377 Munich, Germany
[2] Univ Munich, LMU, Dept Chem & Biochem, D-81377 Munich, Germany
[3] Univ Munich, LMU, CiPSM, D-81377 Munich, Germany
关键词
Antibiotics; inhibitors; protein synthesis; resistance; ribosome; translation; PEPTIDYL-TRANSFERASE CENTER; 23S RIBOSOMAL-RNA; ELONGATION-FACTOR-G; AMINOACYL-TRANSFER-RNA; ESCHERICHIA-COLI RIBOSOMES; TRANSFER RIBONUCLEIC-ACID; ANTIBIOTIC-BINDING-SITES; PHENYLALANYL-OLIGONUCLEOTIDE BINDING; THIOSTREPTON-RESISTANT MUTANTS; LARGE CONFORMATIONAL-CHANGES;
D O I
10.3109/10409230903307311
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
Protein synthesis is one of the major targets in the cell for antibiotics. This review endeavors to provide a comprehensive "post-ribosome structure" A-Z of the huge diversity of antibiotics that target the bacterial translation apparatus, with an emphasis on correlating the vast wealth of biochemical data with more recently available ribosome structures, in order to understand function. The binding site, mechanism of action, and modes of resistance for 26 different classes of protein synthesis inhibitors are presented, ranging from ABT-773 to Zyvox. In addition to improving our understanding of the process of translation, insight into the mechanism of action of antibiotics is essential to the development of novel and more effective antimicrobial agents to combat emerging bacterial resistance to many clinically-relevant drugs.
引用
收藏
页码:393 / 433
页数:41
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