Scanning of 16S Ribosomal RNA for Peptide Nucleic Acid Targets

被引:17
作者
Gorska, Anna [1 ]
Markowska-Zagrajek, Agnieszka [1 ,2 ]
Rownicki, Marcin [1 ,3 ]
Trylska, Joanna [1 ]
机构
[1] Univ Warsaw, Ctr New Technol, Banacha 2C, PL-02097 Warsaw, Poland
[2] Univ Warsaw, Dept Biol, Miecznikowa 1, PL-02096 Warsaw, Poland
[3] Coll Interfac Individual Studies Math & Nat Sci, Banacha 2C, PL-02097 Warsaw, Poland
关键词
DELETERIOUS MUTATIONS; PATHOGENIC BACTERIA; MOLECULAR-DYNAMICS; SEQUENCE; SUBUNIT; ANTIBIOTICS; TRANSLATION; INHIBITION; DATABASE; BINDING;
D O I
10.1021/acs.jpcb.6b02081
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We have designed a protocol and server to aid in the search for putative binding sites in 16S rRNA that could be targeted by peptide nucleic acid oligomers. Various features of 16S rRNA were considered to score its regions as potential targets for sequence-specific binding that could result in inhibition of ribosome function. Specifically, apart from the functional importance of a particular rRNA region, we calculated its accessibility, flexibility, energetics of strand invasion by an oligomer, as well as similarity to human rRNA. To determine 16S rRNA flexibility in the ribosome context, we performed all-atom molecular dynamics simulations of the 30S subunit in explicit solvent. We proposed a few 16S RNA target sites, and one of them was tested experimentally to verify inhibition of bacterial growth by a peptide nucleic acid oligomer.
引用
收藏
页码:8369 / 8378
页数:10
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