Buonvino Silvia, Melino Sonia
Department of Chemical Science and Technologies, University of Rome "Tor Vergata", via della Ricerca Scientifica 1, 00133 Rome, Italy.
Cell Death Discov. 2020 Nov 27;6:134. doi: 10.1038/s41420-020-00372-1. eCollection 2020.
Coagulopathy and syncytial formation are relevant effects of the SARS-CoV-2 infection, but the underlying molecular mechanisms triggering these processes are not fully elucidated. Here, we identified a potential consensus pattern in the Spike S glycoprotein present within the cytoplasmic domain; this consensus pattern was detected in only 79 out of 561,000 proteins (UniProt bank). Interestingly, the pattern was present in both human and bat the coronaviruses S proteins, in many proteins involved in coagulation process, cell-cell interaction, protein aggregation and regulation of cell fate, such as von Willebrand factor, coagulation factor X, fibronectin and Notch, characterized by the presence of the cysteine-rich EGF-like domain. This finding may suggest functional similarities between the matched proteins and the CoV-2 S protein, implying a new possible involvement of the S protein in the molecular mechanism that leads to the coagulopathy and cell fusion in COVID-19 disease.
凝血障碍和合体形成是SARS-CoV-2感染的相关效应,但引发这些过程的潜在分子机制尚未完全阐明。在此,我们在细胞质结构域内的刺突S糖蛋白中鉴定出一种潜在的共有模式;在561,000种蛋白质(UniProt数据库)中,只有79种检测到这种共有模式。有趣的是,这种模式存在于人类和蝙蝠冠状病毒的S蛋白中,也存在于许多参与凝血过程、细胞间相互作用、蛋白质聚集和细胞命运调控的蛋白质中,如血管性血友病因子、凝血因子X、纤连蛋白和Notch,其特征是存在富含半胱氨酸的表皮生长因子样结构域。这一发现可能表明匹配蛋白与CoV-2 S蛋白之间存在功能相似性,这意味着S蛋白可能在导致COVID-19疾病凝血障碍和细胞融合的分子机制中发挥新的作用。