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病毒感染途径中的肌球蛋白马达蛋白。

Myosin motors on the pathway of viral infections.

作者信息

Matozo Tais, Kogachi Leticia, de Alencar Bruna Cunha

机构信息

Departamento de Imunologia, Instituto de Ciencias Biomedicas, Universidade de Sao Paulo, Sao Paulo, Brazil.

出版信息

Cytoskeleton (Hoboken). 2022 Jun;79(6-8):41-63. doi: 10.1002/cm.21718. Epub 2022 Jul 22.

Abstract

Molecular motors are microscopic machines that use energy from adenosine triphosphate (ATP) hydrolysis to generate movement. While kinesins and dynein are molecular motors associated with microtubule tracks, myosins bind to and move on actin filaments. Mammalian cells express several myosin motors. They power cellular processes such as endo- and exocytosis, intracellular trafficking, transcription, migration, and cytokinesis. As viruses navigate through cells, they may take advantage or be hindered by host components and machinery, including the cytoskeleton. This review delves into myosins' cell roles and compares them to their reported functions in viral infections. In most cases, the previously described myosin functions align with their reported role in viral infections, although not in all cases. This opens the possibility that knowledge obtained from studying myosins in viral infections might shed light on new physiological roles for myosins in cells. However, given the high number of myosins expressed and the variety of viruses investigated in the different studies, it is challenging to infer whether the interactions found are specific to a single virus or can be applied to other viruses with the same characteristics. We conclude that the participation of myosins in viral cycles is still a largely unexplored area, especially concerning unconventional myosins.

摘要

分子马达是利用三磷酸腺苷(ATP)水解产生的能量来产生运动的微观机器。驱动蛋白和动力蛋白是与微管轨道相关的分子马达,而肌球蛋白则与肌动蛋白丝结合并在其上移动。哺乳动物细胞表达多种肌球蛋白马达。它们为诸如胞吞作用和胞吐作用、细胞内运输、转录、迁移和胞质分裂等细胞过程提供动力。当病毒在细胞中穿行时,它们可能会利用宿主成分和机制,包括细胞骨架,也可能会受到其阻碍。这篇综述深入探讨了肌球蛋白在细胞中的作用,并将它们与在病毒感染中报道的功能进行了比较。在大多数情况下,先前描述的肌球蛋白功能与其在病毒感染中的报道作用相符,尽管并非在所有情况下都是如此。这就带来了一种可能性,即从研究病毒感染中的肌球蛋白获得的知识可能会揭示肌球蛋白在细胞中的新生理作用。然而,鉴于不同研究中表达的肌球蛋白数量众多且所研究的病毒种类繁多,推断所发现的相互作用是特定于单一病毒还是可应用于具有相同特征的其他病毒具有挑战性。我们得出结论,肌球蛋白在病毒周期中的参与仍然是一个很大程度上未被探索的领域,尤其是关于非常规肌球蛋白。

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