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使用计算筛选进行 COVID-19 的药物再利用:福他替尼/ R406 是一种潜在的候选药物吗?

Drug repurposing for COVID-19 using computational screening: Is Fostamatinib/R406 a potential candidate?

机构信息

Department of Computer Science & Engineering, Institute of Engineering & Management, Salt Lake Electronics Complex, Kolkata 700091, West Bengal, India.

Department of Computer Science & Engineering, University of Engineering & Management, Kolkata 700156, West Bengal, India; Department of Computer Science & Engineering, Jadavpur University, Jadavpur, Kolkata, West Bengal 700032, India.

出版信息

Methods. 2022 Jul;203:564-574. doi: 10.1016/j.ymeth.2021.08.007. Epub 2021 Aug 27.

Abstract

With the gradual increase in the COVID-19 mortality rate, there is an urgent need for an effective drug/vaccine. Several drugs like Remdesivir, Azithromycin, Favirapir, Ritonavir, Darunavir, etc., are put under evaluation in more than 300 clinical trials to treat COVID-19. On the other hand, several vaccines like Pfizer-BioNTech, Moderna, Johnson & Johnson's Janssen, Sputnik V, Covishield, Covaxin, etc., also evolved from the research study. While few of them already gets approved, others show encouraging results and are still under assessment. In parallel, there are also significant developments in new drug development. But, since the approval of new molecules takes substantial time, drug repurposing studies have also gained considerable momentum. The primary agent of the disease progression of COVID-19 is SARS-CoV2/nCoV, which is believed to have ~89% genetic resemblance with SARS-CoV, a coronavirus responsible for the massive outbreak in 2003. With this hypothesis, Human-SARS-CoV protein interactions are used to develop an in-silico Human-nCoV network by identifying potential COVID-19 human spreader proteins by applying the SIS model and fuzzy thresholding by a possible COVID-19 FDA drugs target-based validation. At first, the complete list of FDA drugs is identified for the level-1 and level-2 spreader proteins in this network, followed by applying a drug consensus scoring strategy. The same consensus strategy is involved in the second analysis but on a curated overlapping set of key genes/proteins identified from COVID-19 symptoms. Validation using subsequent docking study has also been performed on COVID-19 potential drugs with the available major COVID-19 crystal structures whose PDB IDs are: 6LU7, 6M2Q, 6W9C, 6M0J, 6M71 and 6VXX. Our computational study and docking results suggest that Fostamatinib (R406 as its active promoiety) may also be considered as one of the potential candidates for further clinical trials in pursuit to counter the spread of COVID-19.

摘要

随着 COVID-19 死亡率的逐渐上升,急需一种有效的药物/疫苗。瑞德西韦、阿奇霉素、法维拉韦、洛匹那韦、达芦那韦等多种药物正在 300 多项临床试验中进行评估,以治疗 COVID-19。另一方面,辉瑞-生物科技、莫德纳、强生的杨森、卫星 V、Covishield、Covaxin 等多种疫苗也来自于研究。虽然其中一些已经获得批准,但其他疫苗也显示出令人鼓舞的结果,仍在评估中。与此同时,新药研发也取得了重大进展。但是,由于新分子的批准需要大量时间,药物再利用研究也得到了相当大的推动。COVID-19 疾病进展的主要病原体是 SARS-CoV2/nCoV,它与导致 2003 年大规模爆发的冠状病毒 SARS-CoV 有~89%的基因相似性。基于这一假设,人们利用人类与 SARS-CoV 的蛋白质相互作用,通过应用 SIS 模型和模糊阈值,确定潜在的 COVID-19 人类传播蛋白,来开发一个基于 SARS-CoV 药物靶点的 COVID-19 网络。首先,确定该网络中一级和二级传播蛋白的完整 FDA 药物清单,然后应用药物共识评分策略。在第二个分析中也采用了相同的共识策略,但针对的是从 COVID-19 症状中确定的关键基因/蛋白的精选重叠集。还使用随后的对接研究对 COVID-19 潜在药物进行了验证,这些药物的可用主要 COVID-19 晶体结构的 PDB ID 为:6LU7、6M2Q、6W9C、6M0J、6M71 和 6VXX。我们的计算研究和对接结果表明,福他替尼(R406 作为其活性前药)也可能被认为是进一步临床试验的潜在候选药物之一,以对抗 COVID-19 的传播。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e669/8390099/2df213ab8aeb/gr1_lrg.jpg

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