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传染性支气管炎病毒E蛋白和M蛋白的细胞质尾段介导它们之间的相互作用。

The cytoplasmic tails of infectious bronchitis virus E and M proteins mediate their interaction.

作者信息

Corse Emily, Machamer Carolyn E

机构信息

Department of Cell Biology, The Johns Hopkins University School of Medicine, 725 North Wolfe Street, Baltimore, MD 21205, USA.

出版信息

Virology. 2003 Jul 20;312(1):25-34. doi: 10.1016/s0042-6822(03)00175-2.

Abstract

Virus-like particle (VLP) formation by the coronavirus E and M proteins suggests that interactions between these proteins play a critical role in coronavirus assembly. We studied interactions between the infectious bronchitis virus (IBV) E and M proteins using in vivo crosslinking and VLP assembly assays. We show that IBV E and M can be crosslinked to each other in IBV-infected and transfected cells, indicating that they interact. The cytoplasmic tails of both proteins are important for this interaction. We also examined the ability of the mutant and chimeric E and M proteins to form VLPs. IBV M proteins that are missing portions of their cytoplasmic tails or transmembrane regions were not able to support VLP formation, regardless of their ability to be crosslinked to IBV E. Interactions between the E and M proteins and the membrane bilayer are likely to play an important role in VLP formation and virus budding.

摘要

冠状病毒E蛋白和M蛋白形成病毒样颗粒(VLP),这表明这些蛋白之间的相互作用在冠状病毒组装过程中起着关键作用。我们使用体内交联和VLP组装试验研究了传染性支气管炎病毒(IBV)E蛋白和M蛋白之间的相互作用。我们发现,在感染IBV的细胞和转染细胞中,IBV E蛋白和M蛋白可以相互交联,表明它们之间存在相互作用。两种蛋白的细胞质尾巴对这种相互作用很重要。我们还检测了突变型和嵌合型E蛋白和M蛋白形成VLP的能力。缺失部分细胞质尾巴或跨膜区域的IBV M蛋白无法支持VLP的形成,无论它们与IBV E蛋白交联的能力如何。E蛋白和M蛋白与膜双层之间的相互作用可能在VLP形成和病毒出芽过程中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6014/7127533/c17a36e9fb59/gr1.jpg

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