The main protease of SARS-CoV-2 as therapeutic target to development specific drugs to treat COVID-19

R. E. Silva-López
{"title":"The main protease of SARS-CoV-2 as therapeutic target to development specific drugs to treat COVID-19","authors":"R. E. Silva-López","doi":"10.15406/jabb.2020.07.00232","DOIUrl":null,"url":null,"abstract":"The pandemic disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) denominated COVID-19 is an important problem of world public health because do not have specific drugs and vaccines available to control the disease progression and the rapid virusspreading. SARS-CoV-2 genome resemble to other SARS-CoV andMERS-COVcoronaviruses genomes, thus drugs developed for SARS and MERS treatment may be used for COVID-19. The aim of this work is discuss the molecular target of SARS-CoV-2, the main protease, a chymotrypsin-like named as 3CLpro, for a rational devolpment of specific molecules anti-SARS-CoV-2 with broad-spectrum anti-coronavirus activities.This study is a literature mini review using 47 articles obtained from Public Medline and Science directmainly from this year 2020. The coronaviruses infection is mediated by spike protein from viral capsid which bind to ACE2 receptor in the host cells which endocytes the viruses RNA, which is translated to proteins that are cleavead by proteases, mainly the 3CLpro. This enzyme is crucial to SARS-CoV-2 replication and its inhibition can prevent the virus replication. Thus, it is an important coronaviruses target because the amino acid sequence of 3CLpros from SARS, MERS and SARS-CoV-2 have high similarity. In silico studies have been demonstrated that synthetic small molecules, natural products, peptidomimetic inhibitors, and HIV inhibitors had different docking scores with SARS-CoV-23CLpro. However, peptidomimetic inhibitors seems to be better inhibitors to this protease and promise dugs to treat COVID-19 and other diseases caused by coronaviruses","PeriodicalId":15033,"journal":{"name":"Journal of Applied Biotechnology & Bioengineering","volume":"34 2 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Applied Biotechnology & Bioengineering","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15406/jabb.2020.07.00232","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

Abstract

The pandemic disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) denominated COVID-19 is an important problem of world public health because do not have specific drugs and vaccines available to control the disease progression and the rapid virusspreading. SARS-CoV-2 genome resemble to other SARS-CoV andMERS-COVcoronaviruses genomes, thus drugs developed for SARS and MERS treatment may be used for COVID-19. The aim of this work is discuss the molecular target of SARS-CoV-2, the main protease, a chymotrypsin-like named as 3CLpro, for a rational devolpment of specific molecules anti-SARS-CoV-2 with broad-spectrum anti-coronavirus activities.This study is a literature mini review using 47 articles obtained from Public Medline and Science directmainly from this year 2020. The coronaviruses infection is mediated by spike protein from viral capsid which bind to ACE2 receptor in the host cells which endocytes the viruses RNA, which is translated to proteins that are cleavead by proteases, mainly the 3CLpro. This enzyme is crucial to SARS-CoV-2 replication and its inhibition can prevent the virus replication. Thus, it is an important coronaviruses target because the amino acid sequence of 3CLpros from SARS, MERS and SARS-CoV-2 have high similarity. In silico studies have been demonstrated that synthetic small molecules, natural products, peptidomimetic inhibitors, and HIV inhibitors had different docking scores with SARS-CoV-23CLpro. However, peptidomimetic inhibitors seems to be better inhibitors to this protease and promise dugs to treat COVID-19 and other diseases caused by coronaviruses
SARS-CoV-2的主要蛋白酶作为治疗靶点,开发特异性药物治疗COVID-19
由严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)引起的大流行疾病COVID-19是世界公共卫生的一个重要问题,因为没有特定的药物和疫苗可用于控制疾病的进展和病毒的快速传播。SARS- cov -2基因组与其他SARS- cov和MERS- cov -冠状病毒基因组相似,因此为SARS和MERS治疗开发的药物可能用于COVID-19。本工作旨在探讨SARS-CoV-2的分子靶点,即主要蛋白酶,一种名为3CLpro的凝乳胰蛋白酶样酶,以合理开发具有广谱抗冠状病毒活性的特异性抗SARS-CoV-2分子。本研究是对主要从2020年开始从Public Medline和Science direct获取的47篇文章进行文献综述。冠状病毒感染是由病毒衣壳上的刺突蛋白介导的,刺突蛋白与宿主细胞中的ACE2受体结合,宿主细胞内吞病毒RNA,并将其翻译成蛋白酶裂解的蛋白质,主要是3CLpro。这种酶对SARS-CoV-2的复制至关重要,抑制它可以阻止病毒复制。因此,SARS、MERS和SARS- cov -2的3CLpros氨基酸序列具有高度相似性,是冠状病毒的重要靶点。计算机研究表明,合成小分子、天然产物、拟肽抑制剂和HIV抑制剂与SARS-CoV-23CLpro的对接评分不同。然而,拟肽抑制剂似乎是这种蛋白酶的更好抑制剂,有望用于治疗COVID-19和其他由冠状病毒引起的疾病
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信