7AZY

Context-specific inhibition of eukaryotic translation by macrolide antibiotics

これはPDB形式変換不可エントリーです。

7AZY の概要

• エントリーDOI: 10.2210/pdb7azy/pdb
• EMDBエントリー: 11951
• 分子名称: 60S ribosomal protein L8-A, 60S ribosomal protein L13-A, 60S ribosomal protein L26-A, ... (44 entities in total)
• 機能のキーワード: context-specific inhibition, macrolide antibiotic, ribosome, telithromycin
• 由来する生物種: Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast); 詳細
• タンパク質・核酸の鎖数: 42
• 化学式量合計: 1916774.59

構造登録者

Koller, T.O.,Wilson, D.N. (登録日: 2020-11-17, 公開日: 2021-05-19, 最終更新日: 2024-07-10)

主引用文献

Svetlov, M.S.,Koller, T.O.,Meydan, S.,Shankar, V.,Klepacki, D.,Polacek, N.,Guydosh, N.R.,Vazquez-Laslop, N.,Wilson, D.N.,Mankin, A.S.
Context-specific action of macrolide antibiotics on the eukaryotic ribosome.
Nat Commun, 12:2803-2803, 2021

PubMed Abstract: Macrolide antibiotics bind in the nascent peptide exit tunnel of the bacterial ribosome and prevent polymerization of specific amino acid sequences, selectively inhibiting translation of a subset of proteins. Because preventing translation of individual proteins could be beneficial for the treatment of human diseases, we asked whether macrolides, if bound to the eukaryotic ribosome, would retain their context- and protein-specific action. By introducing a single mutation in rRNA, we rendered yeast Saccharomyces cerevisiae cells sensitive to macrolides. Cryo-EM structural analysis showed that the macrolide telithromycin binds in the tunnel of the engineered eukaryotic ribosome. Genome-wide analysis of cellular translation and biochemical studies demonstrated that the drug inhibits eukaryotic translation by preferentially stalling ribosomes at distinct sequence motifs. Context-specific action markedly depends on the macrolide structure. Eliminating macrolide-arrest motifs from a protein renders its translation macrolide-tolerant. Our data illuminate the prospects of adapting macrolides for protein-selective translation inhibition in eukaryotic cells.

PubMed: 33990576
DOI: 10.1038/s41467-021-23068-1

実験手法

ELECTRON MICROSCOPY (2.877 Å)