超越运动:扩大黄体病毒运动蛋白的功能范围

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL ACS Infectious Diseases Pub Date : 2024-09-20 DOI:10.1016/j.tplants.2024.09.001
Sara Shakir, Sylvaine Boissinot, Thierry Michon, Stéphane Lafarge, Syed S. Zaidi
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引用次数: 0

摘要

病毒利用其紧凑基因组中编码的蛋白质的潜在多功能能力来建立感染。黄体病毒的 P4 就是这样一种多功能蛋白质。P4由嵌套在衣壳蛋白ORF中的开放阅读框(ORF)表达,它在亚细胞中的定位和相互作用多种多样,反映了它在病毒感染中的复杂作用。在这篇综述中,我们探讨了 P4 如何在重叠 ORF 的限制下进化出多种功能基调。我们分析了这些基调在不同大麦黄矮病毒(BYDV)种类和相关多角体病毒中的保留情况。我们还讨论了病毒蛋白如何在整个感染过程中合作促进病毒的移动和定位。我们深入探讨了未来潜在的研究方向,并提出了开发潜在抗病毒方法的策略。
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Beyond movement: expanding functional landscape of luteovirus movement proteins

Viruses explore the potential multifunctional capacity of the proteins encoded in their compact genome to establish infection. P4 of luteoviruses has emerged as one such multifunctional protein. Expressed from an open reading frame (ORF) nested within coat protein ORF, it displays diverse subcellular localizations and interactions, reflecting its complex role in virus infection. In this review we explore how P4, constrained by overlapping ORFs, has evolved multiple functional motifs. We analyze these motifs’ conservation across different barley yellow dwarf virus (BYDV) species and related poleroviruses. We also discuss how viral proteins cooperate to facilitate movement and localization of the virus throughout infection. We provide insights into potential future research directions and suggest strategies for developing potential antiviral-resistant approaches.

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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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