Targeting monkeypox virus (MPXV): strategies for molecular docking studies on protein inhibition.

IF 1.9 4区 医学 Q3 GENETICS & HEREDITY
Jayant Murlidhar Kushwaha, Majji Sai Sudha Rani, Shilpy Singh
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引用次数: 0

Abstract

In the year 2022, the outbreak of monkeypox virus (MPXV) occurred in the various countries of Africa, particularly Central and West Africa, North America, South America, Europe, and other countries. Without any delay it spread across more than 100 countries infecting around 116,015 people causing around 255 deaths. Monkeypox is a major public health issue, and it is important to search for new therapeutic approaches. This review article is a review of molecular docking studies to identify possible protein inhibition approaches against Monkeypox virus. The exploration on the molecular architecture of the main viral proteins and their relationships with the host cell, emphasizing how these interactions are important in the viral cycle. By gathering data from multiple molecular docking studies, the evaluation of how effective different structural elements are in disrupting these protein interactions is conducted. The results of the analysis reveal how narrowed the focus of molecular interventions is, which holds the promise for the development of antiviral therapies for Monkeypox (Mpox). Not only does this review update the current understanding of the pathophysiology of Monkeypox, but it also provides a basis for more research to deal with this new viral threat. It will be important for the design of inhibitors that can block the replication and dissemination of MPXV to understand the mechanisms of action of the viral proteins and their interactions with the host cell.

靶向猴痘病毒(MPXV):蛋白抑制的分子对接研究策略
在2022年,猴痘病毒(MPXV)在非洲各国,特别是中非和西非、北美、南美、欧洲和其他国家暴发。它迅速蔓延到100多个国家,感染了约11.6015万人,造成约255人死亡。猴痘是一个重大的公共卫生问题,寻找新的治疗方法非常重要。本文综述了分子对接研究在确定猴痘病毒可能的蛋白抑制途径方面的进展。探索主要病毒蛋白的分子结构及其与宿主细胞的关系,强调这些相互作用在病毒周期中的重要性。通过收集来自多个分子对接研究的数据,评估不同结构元件在破坏这些蛋白质相互作用方面的有效性。分析结果揭示了分子干预的焦点是如何缩小的,这为开发猴痘(Mpox)的抗病毒疗法带来了希望。这篇综述不仅更新了目前对猴痘病理生理学的认识,而且还为进一步研究应对这种新的病毒威胁提供了基础。了解病毒蛋白的作用机制及其与宿主细胞的相互作用,对于设计能够阻断MPXV复制和传播的抑制剂具有重要意义。
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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来源期刊
Virus Genes
Virus Genes 医学-病毒学
CiteScore
3.30
自引率
0.00%
发文量
76
审稿时长
3 months
期刊介绍: Viruses are convenient models for the elucidation of life processes. The study of viruses is again on the cutting edge of biological sciences: systems biology, genomics, proteomics, metagenomics, using the newest most powerful tools. Huge amounts of new details on virus interactions with the cell, other pathogens and the hosts – animal (including human), insect, fungal, plant, bacterial, and archaeal - and their role in infection and disease are forthcoming in perplexing details requiring analysis and comments. Virus Genes is dedicated to the publication of studies on the structure and function of viruses and their genes, the molecular and systems interactions with the host and all applications derived thereof, providing a forum for the analysis of data and discussion of its implications, and the development of new hypotheses.
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