A physical model for M1-mediated influenza A virus assembly.

IF 3.2 3区 生物学 Q2 BIOPHYSICS
Julia Peukes, Serge Dmitrieff, François J Nédélec, John A G Briggs
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引用次数: 0

Abstract

Influenza A virus particles assemble at the plasma membrane of infected cells. During assembly all components of the virus come together in a coordinated manner to deform the membrane into a protrusion eventually forming a new, membrane-enveloped virus. Here, we integrate recent molecular insights of this process, particularly concerning the structure of the matrix protein 1 (M1), within a theoretical framework describing the mechanics of virus assembly. Our model describes M1 polymerization and membrane protrusion formation, explaining why it is efficient for M1 to form long strands assembling into helices in filamentous virions. Eventually, we find how the architecture of M1 helices is controlled by physical properties of viral proteins and the host cell membrane. Finally, by considering the growth force and speed of viral filaments, we propose that the helical geometry of M1 strands might have evolved to optimize for fast and efficient virus assembly and growth.

M1 介导的甲型流感病毒组装物理模型。
甲型流感病毒颗粒在受感染细胞的质膜上组装。在组装过程中,病毒的所有成分以一种协调的方式聚集在一起,使膜变形突起,最终形成一种新的膜包膜病毒。在此,我们将最近对这一过程的分子认识,特别是对基质蛋白 1(M1)结构的认识,整合到描述病毒组装力学的理论框架中。我们的模型描述了 M1 的聚合和膜突起的形成,解释了为什么 M1 能有效地形成长链,在丝状病毒中组装成螺旋状。最后,我们发现 M1 螺旋的结构是如何受病毒蛋白质和宿主细胞膜的物理特性控制的。最后,通过考虑病毒丝的生长力和速度,我们提出 M1 螺旋的几何形状可能是为了优化病毒快速高效的组装和生长而进化而来的。
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
Biophysical journal
Biophysical journal 生物-生物物理
CiteScore
6.10
自引率
5.90%
发文量
3090
审稿时长
2 months
期刊介绍: BJ publishes original articles, letters, and perspectives on important problems in modern biophysics. The papers should be written so as to be of interest to a broad community of biophysicists. BJ welcomes experimental studies that employ quantitative physical approaches for the study of biological systems, including or spanning scales from molecule to whole organism. Experimental studies of a purely descriptive or phenomenological nature, with no theoretical or mechanistic underpinning, are not appropriate for publication in BJ. Theoretical studies should offer new insights into the understanding ofexperimental results or suggest new experimentally testable hypotheses. Articles reporting significant methodological or technological advances, which have potential to open new areas of biophysical investigation, are also suitable for publication in BJ. Papers describing improvements in accuracy or speed of existing methods or extra detail within methods described previously are not suitable for BJ.
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