潜在蛋白s1 sars-cov-2配体的建模

S. Bruyakin, D. Makarevich
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引用次数: 0

摘要

SARS-CoV-2的S1蛋白(以下简称S1蛋白)可能是COVID-19发病的主要因素。我们认为,消除或降低这种蛋白质的浓度将减少炎症过程,从而减少激活的免疫系统对器官和组织的损害。对血管紧张素转换酶2 (ACE2)和S1蛋白(ACE2-S1)复合物的分析将确定与S1蛋白结合的寡肽,及时从COVID-19患者血液中去除这些寡肽将防止严重的多器官并发症的发生。此外,与S1蛋白结合的固定化寡肽将能够从体内清除位于细胞外空间的病毒颗粒[1]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MODELING OF POTENTIAL PROTEIN S1 SARS-COV-2 LIGANDS
The S1 protein of SARS-CoV-2 (hereinafter referred to as the S1 protein) is probably the main factor in the pathogenesis of COVID-19. In our opinion, the elimination or decrease in the concentration of this protein will reduce the inflammatory process and, accordingly, damage to organs and tissues by the activated immune system. An analysis of the complexes of the Angiotensin-converting enzyme 2 (ACE2) and the S1 protein (ACE2-S1) will determine the oligopeptides that are ligands for binding the S1 protein, the timely removal of which from the blood of patients with COVID-19 will prevent the development of severe multi-organ complications. Besides, the immobilized oligopeptide that binds the S1 protein will be able to remove from the body viral particles located in the extracellular space [1].
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