The Role of TMPRSS2 and TMPRSS2- Inhibitors in Cell Entry Mechanism of COVID-19

S. Bittmann
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引用次数: 5

Abstract

The enzymes trypsin, furine and other proprotein convertases, cathepsin, transmembrane proteases (TMPRSS) and elastases play a role in the cell entry of coronaviruses (Coronaviridae). The proteases TMPRSS2 and TMPRSS11a, which are abundant in the respiratory tract and expressed on cell surfaces, promote the entry of SARS-CoV-1 viruses. For the TMPRSS protease TMPRSS11d - also known as human airway trypsin-like protease (HAT) - a proteolytic activation of the S- protein of SARS-CoV-1 was demonstrated. TMPRSS2, in turn, complexes with the ACE2 receptor, which allows efficient penetration of the virus directly at the cell surface. TMPRSS2 and TMPRSS11D activate the S protein by cleaving it into the S1 and S2 subunits, thus allowing endosome-independent cell entry at the cell membrane. Virus-based therapies include monoclonal antibodies, antiviral peptides that dock to the S protein of viruses, viral nucleic acid synthesis inhibitors and inhibitors for docking to other viral structures and accessory proteins.
TMPRSS2和TMPRSS2抑制剂在COVID-19细胞进入机制中的作用
胰蛋白酶、糠氨酸等蛋白转化酶、组织蛋白酶、跨膜蛋白酶(TMPRSS)和弹性酶在冠状病毒(冠状病毒科)进入细胞过程中发挥作用。在呼吸道中丰富并在细胞表面表达的蛋白酶TMPRSS2和TMPRSS11a促进了SARS-CoV-1病毒的进入。对于TMPRSS蛋白酶TMPRSS11d,也称为人气道胰蛋白酶样蛋白酶(HAT),证实了SARS-CoV-1的S-蛋白的蛋白水解激活。反过来,TMPRSS2与ACE2受体结合,使病毒能够直接在细胞表面有效地渗透。TMPRSS2和TMPRSS11D通过将S蛋白切割成S1和S2亚基来激活S蛋白,从而允许不依赖于内体的细胞进入细胞膜。基于病毒的治疗包括单克隆抗体、与病毒S蛋白对接的抗病毒肽、病毒核酸合成抑制剂以及与其他病毒结构和辅助蛋白对接的抑制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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