Man'kin A S
Center for Pharmaceutical Biotechnology-m/c 870, University of Illinois, Chicago, Illinois 60607, USA.
Mol Biol (Mosk). 2001 Jul-Aug;35(4):597-609.
In spite of decades of research, our understanding of the principles of antibiotic binding to the ribosome and the mechanisms of drug action remains only fragmentary. Recent progress in biochemical and genetic studies of some "old" and new antibiotics and the availability of high-resolution structures of the ribosome subunits allows mapping the antibiotic-binding sites at atomic resolution. In this review, interaction of three groups of antibiotics with the ribosome and the mechanisms of the drug action are discussed, considering the data used to map the binding sites of the new macrolide derivatives, ketolides, a novel clinically important antibiotic linezolid, and a still experimental drug evernimicin.
尽管经过了数十年的研究,但我们对抗生素与核糖体结合的原理以及药物作用机制的理解仍然支离破碎。近期在一些“老”抗生素和新抗生素的生化及遗传学研究方面取得的进展,以及核糖体亚基高分辨率结构的可得性,使得能够以原子分辨率绘制抗生素结合位点。在这篇综述中,考虑到用于绘制新型大环内酯衍生物、酮内酯、一种临床上重要的新型抗生素利奈唑胺以及一种仍处于实验阶段的药物埃维霉素结合位点的数据,讨论了三类抗生素与核糖体的相互作用以及药物作用机制。