In Silico Screening and Testing of FDA-Approved Small Molecules to Block SARS-CoV-2 Entry to the Host Cell by Inhibiting Spike Protein Cleavage

被引:3
|
作者
Ozdemir, E. Sila [1 ]
Le, Hillary H. [1 ]
Yildirim, Adem [1 ,2 ]
Ranganathan, Srivathsan V. [1 ,2 ]
机构
[1] Oregon Hlth & Sci Univ, Knight Canc Inst, Canc Early Detect Adv Res Ctr, Portland, OR 97201 USA
[2] Oregon Hlth & Sci Univ, Knight Canc Inst, Div Oncol Sci, Portland, OR 97201 USA
来源
VIRUSES-BASEL | 2022年 / 14卷 / 06期
关键词
drug repurposing; SARS-CoV-2; molecular modeling; in silico screening; proteases; RESPIRATORY SYNDROME CORONAVIRUS; CRYSTAL-STRUCTURE; DATABASE; DOCKING; SERINE; MODEL;
D O I
10.3390/v14061129
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The COVID-19 pandemic began in 2019, but it is still active. The development of an effective vaccine reduced the number of deaths; however, a treatment is still needed. Here, we aimed to inhibit viral entry to the host cell by inhibiting spike (S) protein cleavage by several proteases. We developed a computational pipeline to repurpose FDA-approved drugs to inhibit protease activity and thus prevent S protein cleavage. We tested some of our drug candidates and demonstrated a decrease in protease activity. We believe our pipeline will be beneficial in identifying a drug regimen for COVID-19 patients.
引用
收藏
页数:17
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