The Structure, Function, and Mechanisms of Action of Enterovirus Non-structural Protein 2C.
The Structure, Function, and Mechanisms of Action of Enterovirus Non-structural Protein 2C.
复制标题
肠道病毒非结构蛋白2C的结构、功能及作用机制
DOI:
10.3389/fmicb.2020.615965
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发表时间:
2020
影响因子:
5.2
通讯作者:
Du J
中科院分区:
文献类型:
--
作者:
Wang SH;Wang K;Zhao K;Hua SC;Du J
Enteroviruses are a group of RNA viruses belonging to the family Picornaviridae. They include human enterovirus groups A, B, C, and D as well as non-human enteroviruses. Enterovirus infections can lead to hand, foot, and mouth disease and herpangina, whose clinical manifestations are often mild, although some strains can result in severe neurological complications such as encephalitis, myocarditis, meningitis, and poliomyelitis. To date, research on enterovirus non-structural proteins has mainly focused on the 2A and 3C proteases and 3D polymerase. However, another non-structural protein, 2C, is the most highly conserved protein, and plays a vital role in the enterovirus life cycle. There are relatively few studies on this protein. Previous studies have demonstrated that enterovirus 2C is involved in virus uncoating, host cell membrane rearrangements, RNA replication, encapsidation, morphogenesis, ATPase, helicase, and chaperoning activities. Despite ongoing research, little is known about the pathogenesis of enterovirus 2C proteins in viral replication or in the host innate immune system. In this review, we discuss and summarize the current understanding of the structure, function, and mechanism of the enterovirus 2C proteins, focusing on the key mutations and motifs involved in viral infection, replication, and immune regulation. We also focus on recent progress in research into the role of 2C proteins in regulating the pattern recognition receptors and type I interferon signaling pathway to facilitate viral replication. Given these functions and mechanisms, the potential application of the 2C proteins as a target for anti-viral drug development is also discussed. Future studies will focus on the determination of more crystal structures of enterovirus 2C proteins, which might provide more potential targets for anti-viral drug development against enterovirus infections.
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影响因子:
3.1
作者:
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通讯作者:
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影响因子:
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DOI:
10.1006/bbrc.1995.1010
发表时间:
1995-01-05
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作者:
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