基孔肯雅病毒及其跨框架变异病毒孔蛋白不同膜活性的机制研究。

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Infectious Diseases Pub Date : 2025-02-14 Epub Date: 2025-01-02 DOI:10.1021/acsinfecdis.4c00562
Kirti Suhag, Subhomoi Borkotoky, Shumaila Iqbal Siddiqui, Jitender Kumar, Chandra Shekhar Kumar, Pushkar Tatiya, Subhendu Ghosh, Manidipa Banerjee
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引用次数: 0

摘要

甲病毒是托加病毒科的一种媒介传播病毒,在感染过程中编码一个小的离子通道形成蛋白6K及其转框变体(TF)。虽然6K/TF在糖蛋白运输、病毒组装和出芽中起着至关重要的作用,但没有对这些功能的机制解释。我们研究了蚊媒甲病毒基孔肯雅病毒中6K和TF的不同生化功能。我们发现,像6K一样,TF也能够在双层膜中形成离子通道。6K在膜上形成的组装体比TF形成的组装体结构更复杂,并且可能具有更多的离子限制性。6K和TF都对内质网膜有很强的亲和力,这表明这些成分在质膜上的定位,如先前报道的那样,要么与翻译后修饰有关,要么通过与结合伙伴的相互作用介导。这些结构和功能的见解可能阐明6K和TF在甲病毒生命周期中的不同作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechanistic Insights into the Divergent Membrane Activities of a Viroporin from Chikungunya Virus and Its Transframe Variant.

Alphaviruses, a genus of vector-borne viruses in the Togaviridae family, encode a small ion-channel-forming protein, 6K, and its transframe variant (TF) during infections. Although 6K/TF have vital roles in glycoprotein transport, virus assembly, and budding, there is no mechanistic explanation for these functions. We investigated the distinct biochemical functionalities of 6K and TF from the mosquito-borne alphavirus, Chikungunya Virus. We show that like 6K, TF is also capable of forming ion channels in bilayer membranes. The assemblies formed by 6K in membranes are structurally more complex and potentially more ion-restrictive than those formed by TF. Both 6K and TF show strong affinity toward the ER membranes, indicating that the localization of these components at the plasma membrane, as previously reported, is either linked to post-translational modification or mediated through interaction with binding partners. These structural and functional insights may elucidate the distinct roles of 6K and TF in the alphavirus life cycle.

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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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