Department of Family Medicine, Yonsei University College of Medicine, 50-1 Yonsei-ro, Seodaemun-gu, Seoul 120-752, Korea.
Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Khalid University, Abha 61421, Saudi Arabia.
Molecules. 2021 Mar 17;26(6):1678. doi: 10.3390/molecules26061678.
The COVID-19 outbreak continues to spread worldwide at a rapid rate. Currently, the absence of any effective antiviral treatment is the major concern for the global population. The reports of the occurrence of various point mutations within the important therapeutic target protein of SARS-CoV-2 has elevated the problem. The SARS-CoV-2 main protease (Mpro) is a major therapeutic target for new antiviral designs. In this study, the efficacy of PF-00835231 was investigated (a Mpro inhibitor under clinical trials) against the Mpro and their reported mutants. Various in silico approaches were used to investigate and compare the efficacy of PF-00835231 and five drugs previously documented to inhibit the Mpro. Our study shows that PF-00835231 is not only effective against the wild type but demonstrates a high affinity against the studied mutants as well.
新型冠状病毒(COVID-19)疫情正在全球迅速蔓延。目前,缺乏有效的抗病毒治疗方法是全球关注的主要问题。有报道称,SARS-CoV-2 的重要治疗靶蛋白中发生了各种点突变,使这一问题更加严重。SARS-CoV-2 主要蛋白酶(Mpro)是新型抗病毒设计的主要治疗靶标。在这项研究中,研究了 PF-00835231 的疗效(一种处于临床试验阶段的 Mpro 抑制剂),以对抗 Mpro 及其报道的突变体。使用各种计算机模拟方法来研究和比较 PF-00835231 和之前已被证明抑制 Mpro 的五种药物的疗效。我们的研究表明,PF-00835231 不仅对野生型有效,而且对研究的突变体也具有很高的亲和力。