Binding of aminoglycoside antibiotics to the small ribosomal subunit: A continuum electrostatics investigation

被引:48
作者
Ma, CS
Baker, NA
Joseph, S
McCammon, JA
机构
[1] Univ Calif San Diego, Howard Hughes Med Inst, Dept Chem & Biochem, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
[3] Yale Univ, Dept Chem, New Haven, CT 06520 USA
关键词
D O I
10.1021/ja016830+
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The binding of paromomycin and similar antibiotics to the small (30S) ribosomal subunit has been studied using continuum electrostatics methods. Crystallographic information from a complex of paromomycin with the 30S subunit was used as a framework to develop structures of similar antibiotics in the same ribosomal binding site. Total binding energies were calculated from electrostatic properties obtained by solution of the Poisson-Boltzmann equation combined with a surface area-dependent apolar term. These computed results showed good correlation with experimental data. Additionally, calculation of the ribosomal electrostatic potential in the paromomycin binding site provided insight into the electrostatic mechanisms for aminoglycoside binding and clues for the rational design of more effective antibiotics.
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收藏
页码:1438 / 1442
页数:5
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