Current status of structure-based drug repurposing against COVID-19 by targeting SARS-CoV-2 proteins.

Biophysics and Physicobiology Pub Date : 2021-10-05 eCollection Date: 2021-01-01 DOI:10.2142/biophysico.bppb-v18.025
Atsushi Hijikata, Clara Shionyu, Setsu Nakae, Masafumi Shionyu, Motonori Ota, Shigehiko Kanaya, Tsuyoshi Shirai
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Abstract

More than one and half years have passed, as of August 2021, since the COVID-19 caused by the novel coronavirus named SARS-CoV-2 emerged in 2019. While the recent success of vaccine developments likely reduces the severe cases, there is still a strong requirement of safety and effective therapeutic drugs for overcoming the unprecedented situation. Here we review the recent progress and the status of the drug discovery against COVID-19 with emphasizing a structure-based perspective. Structural data regarding the SARS-CoV-2 proteome has been rapidly accumulated in the Protein Data Bank, and up to 68% of the total amino acid residues encoded in the genome were covered by the structural data. Despite a global effort of in silico and in vitro screenings for drug repurposing, there is only a limited number of drugs had been successfully authorized by drug regulation organizations. Although many approved drugs and natural compounds, which exhibited antiviral activity in vitro, were considered potential drugs against COVID-19, a further multidisciplinary investigation is required for understanding the mechanisms underlying the antiviral effects of the drugs.

Abstract Image

Abstract Image

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通过靶向 SARS-CoV-2 蛋白对 COVID-19 进行基于结构的药物再利用的现状。
自 2019 年出现由名为 SARS-CoV-2 的新型冠状病毒引起的 COVID-19 以来,截至 2021 年 8 月已过去了一年半的时间。虽然近期疫苗研发的成功可能会减少严重病例的发生,但要克服这一前所未有的局面,仍然非常需要安全有效的治疗药物。在此,我们回顾了针对 COVID-19 的药物研发的最新进展和现状,并强调了基于结构的视角。蛋白质数据库(Protein Data Bank)迅速积累了有关 SARS-CoV-2 蛋白质组的结构数据,结构数据涵盖了基因组编码的氨基酸残基总数的 68%。尽管全球都在努力进行药物再利用的硅学和体外筛选,但成功获得药物监管机构授权的药物数量有限。虽然许多已获批准的药物和天然化合物在体外表现出抗病毒活性,被认为是抗 COVID-19 的潜在药物,但要了解这些药物的抗病毒作用机制还需要进一步的多学科研究。
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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