Suppr超能文献

四种大环内酯类抗生素与核糖体大亚基结合的结构。

The structures of four macrolide antibiotics bound to the large ribosomal subunit.

作者信息

Hansen Jeffrey L, Ippolito Joseph A, Ban Nenad, Nissen Poul, Moore Peter B, Steitz Thomas A

机构信息

Department of Molecular Biophysics and Biochemistry, New Haven, Connecticut 06520, USA.

出版信息

Mol Cell. 2002 Jul;10(1):117-28. doi: 10.1016/s1097-2765(02)00570-1.

Abstract

Crystal structures of the Haloarcula marismortui large ribosomal subunit complexed with the 16-membered macrolide antibiotics carbomycin A, spiramycin, and tylosin and a 15-membered macrolide, azithromycin, show that they bind in the polypeptide exit tunnel adjacent to the peptidyl transferase center. Their location suggests that they inhibit protein synthesis by blocking the egress of nascent polypeptides. The saccharide branch attached to C5 of the lactone rings extends toward the peptidyl transferase center, and the isobutyrate extension of the carbomycin A disaccharide overlaps the A-site. Unexpectedly, a reversible covalent bond forms between the ethylaldehyde substituent at the C6 position of the 16-membered macrolides and the N6 of A2103 (A2062, E. coli). Mutations in 23S rRNA that result in clinical resistance render the binding site less complementary to macrolides.

摘要

嗜盐栖热放线菌大核糖体亚基与16元大环内酯类抗生素碳霉素A、螺旋霉素和泰乐菌素以及15元大环内酯类阿奇霉素形成的晶体结构表明,它们结合在肽基转移酶中心附近的多肽出口通道中。它们的位置表明,它们通过阻断新生多肽的出口来抑制蛋白质合成。连接在内酯环C5上的糖分支向肽基转移酶中心延伸,碳霉素A二糖的异丁酸延伸部分与A位点重叠。出乎意料的是,16元大环内酯类化合物C6位的乙醛取代基与A2103(大肠杆菌中的A2062)的N6之间形成了可逆共价键。导致临床耐药性的23S rRNA突变使结合位点与大环内酯类的互补性降低。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验