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
论文数: 0引用数: 0
h-index: 0
机构:
Oregon Hlth & Sci Univ, Knight Canc Inst, Canc Early Detect Adv Res Ctr, Portland, OR 97201 USAOregon Hlth & Sci Univ, Knight Canc Inst, Canc Early Detect Adv Res Ctr, Portland, OR 97201 USA
Ozdemir, E. Sila
[1
]
Le, Hillary H.
论文数: 0引用数: 0
h-index: 0
机构:
Oregon Hlth & Sci Univ, Knight Canc Inst, Canc Early Detect Adv Res Ctr, Portland, OR 97201 USAOregon Hlth & Sci Univ, Knight Canc Inst, Canc Early Detect Adv Res Ctr, Portland, OR 97201 USA
Le, Hillary H.
[1
]
Yildirim, Adem
论文数: 0引用数: 0
h-index: 0
机构:
Oregon Hlth & Sci Univ, Knight Canc Inst, Canc Early Detect Adv Res Ctr, Portland, OR 97201 USA
Oregon Hlth & Sci Univ, Knight Canc Inst, Div Oncol Sci, Portland, OR 97201 USAOregon Hlth & Sci Univ, Knight Canc Inst, Canc Early Detect Adv Res Ctr, Portland, OR 97201 USA
Yildirim, Adem
[1
,2
]
Ranganathan, Srivathsan V.
论文数: 0引用数: 0
h-index: 0
机构:
Oregon Hlth & Sci Univ, Knight Canc Inst, Canc Early Detect Adv Res Ctr, Portland, OR 97201 USA
Oregon Hlth & Sci Univ, Knight Canc Inst, Div Oncol Sci, Portland, OR 97201 USAOregon Hlth & Sci Univ, Knight Canc Inst, Canc Early Detect Adv Res Ctr, Portland, OR 97201 USA
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.