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与严重急性呼吸综合征冠状病毒2(SARS-CoV-2)靶点跨膜丝氨酸蛋白酶2(TMPRSS2)结合的实验性药物的结构分析

Structural analysis of experimental drugs binding to the SARS-CoV-2 target TMPRSS2.

作者信息

Huggins David J

机构信息

Tri-Institutional Therapeutics Discovery Institute, New York, NY, USA; Department of Physiology and Biophysics, Weill Cornell Medical College of Cornell University, New York, NY, USA.

出版信息

J Mol Graph Model. 2020 Nov;100:107710. doi: 10.1016/j.jmgm.2020.107710. Epub 2020 Aug 11.

Abstract

The emergence of SARS-CoV-2 has prompted a worldwide health emergency. There is an urgent need for therapeutics, both through the repurposing of approved drugs and the development of new treatments. In addition to the viral drug targets, a number of human drug targets have been suggested. In theory, targeting human proteins should provide an advantage over targeting viral proteins in terms of drug resistance, which is commonly a problem in treating RNA viruses. This paper focuses on the human protein TMPRSS2, which supports coronavirus life cycles by cleaving viral spike proteins. The three-dimensional structure of TMPRSS2 is not known and so we have generated models of the TMPRSS2 in the apo state as well as in complex with a peptide substrate and putative inhibitors to aid future work. Importantly, many related human proteases have 80% or higher identity with TMPRSS2 in the S1-S1' subsites, with plasminogen and urokinase-type plasminogen activator (uPA) having 95% identity. We highlight 376 approved, investigational or experimental drugs targeting S1A serine proteases that may also inhibit TMPRSS2. Whilst the presence of a relatively uncommon lysine residue in the S2/S3 subsites means that some serine protease inhibitors will not inhibit TMPRSS2, this residue is likely to provide a handle for selective targeting in a focused drug discovery project. We discuss how experimental drugs targeting related serine proteases might be repurposed as TMPRSS2 inhibitors to treat coronaviruses.

摘要

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的出现引发了全球卫生紧急事件。迫切需要通过重新利用已批准药物和开发新疗法来获得治疗方法。除了病毒药物靶点外,还提出了一些人类药物靶点。理论上,靶向人类蛋白质在耐药性方面应比靶向病毒蛋白质具有优势,而耐药性通常是治疗RNA病毒时的一个问题。本文重点关注人类蛋白质跨膜丝氨酸蛋白酶2(TMPRSS2),它通过切割病毒刺突蛋白来支持冠状病毒的生命周期。TMPRSS2的三维结构尚不清楚,因此我们生成了其无配体状态以及与肽底物和推定抑制剂复合物的模型,以辅助未来的研究工作。重要的是,许多相关的人类蛋白酶在S1-S1'亚位点与TMPRSS2的同源性达到80%或更高,纤溶酶原和尿激酶型纤溶酶原激活剂(uPA)的同源性为95%。我们重点介绍了376种已批准、正在研究或实验性的靶向S1A丝氨酸蛋白酶的药物,这些药物也可能抑制TMPRSS2。虽然S2/S3亚位点中存在一个相对不常见的赖氨酸残基意味着一些丝氨酸蛋白酶抑制剂不会抑制TMPRSS2,但这个残基可能为在专注的药物发现项目中进行选择性靶向提供一个切入点。我们讨论了如何将靶向相关丝氨酸蛋白酶的实验性药物重新用作TMPRSS2抑制剂来治疗冠状病毒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e4f/7417922/583599bc518c/fx1_lrg.jpg

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