Small Molecules Targeting Viral RNA

被引:3
|
作者
Mathez, Gregory [1 ]
Cagno, Valeria [1 ]
机构
[1] Univ Lausanne, Univ Hosp Lausanne, Inst Microbiol, CH-1011 Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
antiviral; RNA; SARS-CoV-2; IRES; programmed ribosomal frameshift; HEPATITIS-C VIRUS; BINDING SMALL MOLECULES; RESPONSE ELEMENT RRE; TAT-TAR INTERACTION; BIOLOGICAL EVALUATION; SARS-CORONAVIRUS; HIV-1; SITE; RIBOSOME; DISCOVERY;
D O I
10.3390/ijms241713500
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The majority of antivirals available target viral proteins; however, RNA is emerging as a new and promising antiviral target due to the presence of highly structured RNA in viral genomes fundamental for their replication cycle. Here, we discuss methods for the identification of RNA-targeting compounds, starting from the determination of RNA structures either from purified RNA or in living cells, followed by in silico screening on RNA and phenotypic assays to evaluate viral inhibition. Moreover, we review the small molecules known to target the programmed ribosomal frameshifting element of SARS-CoV-2, the internal ribosomal entry site of different viruses, and RNA elements of HIV.
引用
收藏
页数:16
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