Inhibition of translation termination by small molecules targeting ribosomal release factors

被引:7
|
作者
Ge, Xueliang [1 ]
Oliveira, Ana [1 ]
Hjort, Karin [2 ]
Bergfors, Terese [1 ]
de Teran, Hugo Gutierrez [1 ]
Andersson, Dan I. [2 ]
Sanyal, Suparna [1 ]
Aqvist, Johan [1 ]
机构
[1] Uppsala Univ, Dept Cell & Mol Biol, Biomed Ctr, SE-75124 Uppsala, Sweden
[2] Uppsala Univ, Dept Med Biochem & Microbiol, Biomed Ctr, SE-75124 Uppsala, Sweden
基金
瑞典研究理事会;
关键词
CRYSTAL-STRUCTURE; CODON RECOGNITION; PEPTIDE RELEASE; BLASTICIDIN S; TRANSFER-RNA; BACTERIAL; GENERATION; PREDICTION; MECHANISM; ACCURACY;
D O I
10.1038/s41598-019-51977-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The bacterial ribosome is an important drug target for antibiotics that can inhibit different stages of protein synthesis. Among the various classes of compounds that impair translation there are, however, no known small-molecule inhibitors that specifically target ribosomal release factors (RFs). The class I RFs are essential for correct termination of translation and they differ considerably between bacteria and eukaryotes, making them potential targets for inhibiting bacterial protein synthesis. We carried out virtual screening of a large compound library against 3D structures of free and ribosome-bound RFs in order to search for small molecules that could potentially inhibit termination by binding to the RFs. Here, we report identification of two such compounds which are found both to bind free RFs in solution and to inhibit peptide release on the ribosome, without affecting peptide bond formation.
引用
收藏
页数:10
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