Department of Chemistry & Biomolecular Science, Clarkson University, 8 Clarkson Avenue, Potsdam, NY, 13699-5820, USA.
Immunol Res. 2022 Apr;70(2):143-151. doi: 10.1007/s12026-021-09250-z. Epub 2021 Nov 16.
The severity of COVID-19 has been observed throughout the world as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) globally claimed more than 2 million lives and left a devastating impact worldwide. Recently several virulent mutant strains of this virus, such as the B.1.1.7, B.1.351, and P1 lineages, have emerged with initial predominance in UK, South Africa, and Brazil. Another extremely pathogenic B.1.617 lineage and its sub-lineages, first detected in India, are now affecting some countries at notably stronger spread-rates. The present paper computationally examines the time-based structures of B.1.1.7, B.1.351, and P1 lineages with selected spike protein mutations. The mutations in the more recently found B.1.617 lineage and its sub-lineages are explored, and the implications for multiple point mutations of the spike protein's receptor-binding domain (RBD) are described. The selected S1 mutations within the highly contagious B.1.617.2 sub-lineage, also known as the delta variant, are examined as well.
新冠病毒疾病(COVID-19)的严重程度在全球范围内都有所体现,严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)已在全球范围内导致超过 200 万人死亡,并在全球范围内造成毁灭性影响。最近,该病毒出现了几种毒性更强的突变株,如 B.1.1.7、B.1.351 和 P1 谱系,最初在英国、南非和巴西占主导地位。另一种极其致命的 B.1.617 谱系及其亚谱系,最初在印度发现,目前正在一些国家以更高的传播速度传播。本文通过计算机模拟分析了 B.1.1.7、B.1.351 和 P1 谱系中与选定刺突蛋白突变相关的时间结构。还对最近发现的 B.1.617 谱系及其亚谱系中的突变进行了探索,并描述了其对刺突蛋白受体结合域(RBD)的多个点突变的影响。还对高度传染性的 B.1.617.2 亚谱系中(又称 delta 变体)的选定 S1 突变进行了检查。