Macrolide antibiotics: Binding site, mechanism of action, resistance

被引:153
作者
Gaynor, M [1 ]
Mankin, AS [1 ]
机构
[1] Univ Illinois, Ctr Pharmaceut Biotechnol, Chicago, IL 60607 USA
关键词
macrolides; erythromycin; ketolides; azithromycin; clarithromycin; tylosin; carbomycin; spiramycin; ribosome; resistance;
D O I
10.2174/1568026033452159
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Macrolides are among the most clinically important antibiotics. However, many aspects of macrolide action and resistance remain obscure. In this review we summarize the current knowledge, as well as unsolved questions, regarding the principles of macrolide binding to the large ribosomal subunit and the mechanism of drug action. Two mechanisms of macrolide resistance, inducible expression of Erin methyltransferase and peptide-mediated resistance, appear to depend on specific interactions between the ribosome-bound macrolide molecule and the nascent peptide. The similarity between these mechanisms and their relation to the general mode of macrolide action is discussed and the discrepancies between currently available data are highlighted.
引用
收藏
页码:949 / 960
页数:12
相关论文
共 62 条
[1]   MUTANT DNAK CHAPERONES CAUSE RIBOSOME ASSEMBLY DEFECTS IN ESCHERICHIA-COLI [J].
ALIX, JH ;
GUERIN, MF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (20) :9725-9729
[2]   The complete atomic structure of the large ribosomal subunit at 2.4 Å resolution [J].
Ban, N ;
Nissen, P ;
Hansen, J ;
Moore, PB ;
Steitz, TA .
SCIENCE, 2000, 289 (5481) :905-920
[3]   NASCENT POLYPEPTIDE-CHAINS EMERGE FROM THE EXIT DOMAIN OF THE LARGE RIBOSOMAL-SUBUNIT - IMMUNE MAPPING OF THE NASCENT CHAIN [J].
BERNABEU, C ;
LAKE, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (10) :3111-3115
[4]   Studies of the novel ketolide ABT-773:: Transport, binding to ribosomes, and inhibition of protein synthesis in Streptococcus pneumoniae [J].
Capobianco, JO ;
Cao, ZS ;
Shortridge, VD ;
Ma, ZK ;
Flamm, RK ;
Zhong, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (06) :1562-1567
[5]   Ribbons [J].
Carson, M .
MACROMOLECULAR CRYSTALLOGRAPHY, PT B, 1997, 277 :493-505
[6]   A comparison of the inhibition of translation and 50S ribosomal subunit formation in Staphylococcus aureus cells by nine different macrolide antibiotics [J].
Champney, WS ;
Tober, CL ;
Burdine, R .
CURRENT MICROBIOLOGY, 1998, 37 (06) :412-417
[7]   Inhibition of translation and 50S ribosomal subunit formation in Staphylococcus aureus cells by 11 different ketolide antibiotics [J].
Champney, WS ;
Tober, CL .
CURRENT MICROBIOLOGY, 1998, 37 (06) :418-425
[8]   MACROLIDE ANTIBIOTICS INHIBIT 50S RIBOSOMAL-SUBUNIT ASSEMBLY IN BACILLUS-SUBTILIS AND STAPHYLOCOCCUS-AUREUS [J].
CHAMPNEY, WS ;
BURDINE, R .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1995, 39 (09) :2141-2144
[9]   ERYTHROMYCIN INHIBITS THE ASSEMBLY OF THE LARGE RIBOSOMAL-SUBUNIT IN GROWING ESCHERICHIA-COLI-CELLS [J].
CHITTUM, HS ;
CHAMPNEY, WS .
CURRENT MICROBIOLOGY, 1995, 30 (05) :273-279
[10]   RIBOSOMAL-PROTEIN GENE SEQUENCE CHANGES IN ERYTHROMYCIN-RESISTANT MUTANTS OF ESCHERICHIA-COLI [J].
CHITTUM, HS ;
CHAMPNEY, WS .
JOURNAL OF BACTERIOLOGY, 1994, 176 (20) :6192-6198