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用于研究肌动蛋白网络结构和动力学的重组系统。

Reconstituted systems for studying the architecture and dynamics of actin networks.

作者信息

Cantat Alice, Colin Alexandra

机构信息

Interdisciplinary Research Institute of Grenoble, Laboratoire de Physiologie Cellulaire & Végétale, CytoMorpho Lab, University of Grenoble-Alpes, CEA, CNRS, INRA, Grenoble, France.

出版信息

Biochem J. 2025 May 23;482(11):691-708. doi: 10.1042/BCJ20253044.

DOI:10.1042/BCJ20253044
PMID:40411213
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12203972/
Abstract

Actin, a ubiquitous protein essential for numerous cellular functions, is found in all eukaryotes. Despite extensive research across molecular to organismal scales, fundamental questions persist regarding the regulation of dynamic actin architectures, their interaction with membranes, and their mechanical properties. Characterizing the factors governing these processes presents significant challenges. This review emphasizes the value of simplified, reconstituted systems in addressing these unresolved questions. We particularly highlight the critical importance of macroscopic, network-level reconstitutions for tackling these issues. We first describe the available methodological toolkit for (1) controlling actin polymerization spatiotemporally and (2) confining actin networks within closed environments to examine boundary constraint effects or the impact of limited component availability on network properties. We then review studies employing these reconstituted systems to investigate how actin architecture influences various processes and how dynamic actin structures are established and maintained. Further, we discuss how network-level reconstitutions have enhanced our understanding of actin networks' mechanical properties and their interaction with the lipid membranes. Throughout the review, we discuss future perspectives for each topic and explain how macroscale reconstitutions can provide deeper mechanistic insights into actin-related processes.

摘要

肌动蛋白是一种对众多细胞功能至关重要的普遍存在的蛋白质,存在于所有真核生物中。尽管在从分子到生物体尺度上进行了广泛研究,但关于动态肌动蛋白结构的调控、它们与膜的相互作用以及它们的机械性能等基本问题仍然存在。表征控制这些过程的因素面临重大挑战。本综述强调了简化的、重构系统在解决这些未解决问题方面的价值。我们特别强调宏观的、网络水平的重构对于解决这些问题的至关重要性。我们首先描述了用于(1)时空控制肌动蛋白聚合以及(2)将肌动蛋白网络限制在封闭环境中以检查边界约束效应或有限成分可用性对网络性质影响的可用方法工具包。然后,我们回顾了利用这些重构系统来研究肌动蛋白结构如何影响各种过程以及动态肌动蛋白结构是如何建立和维持的研究。此外,我们讨论了网络水平的重构如何增强了我们对肌动蛋白网络机械性能及其与脂质膜相互作用的理解。在整个综述中,我们讨论了每个主题的未来前景,并解释了宏观尺度的重构如何能够为肌动蛋白相关过程提供更深入的机制见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd4/12203972/d0a2d2c205bd/BCJ-482-11-BCJ20253044-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd4/12203972/1adad0866074/BCJ-482-11-BCJ20253044-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd4/12203972/f037225055fa/BCJ-482-11-BCJ20253044-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd4/12203972/d0a2d2c205bd/BCJ-482-11-BCJ20253044-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd4/12203972/1adad0866074/BCJ-482-11-BCJ20253044-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd4/12203972/f037225055fa/BCJ-482-11-BCJ20253044-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bd4/12203972/d0a2d2c205bd/BCJ-482-11-BCJ20253044-g003.jpg

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本文引用的文献

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Balancing limited resources in actin network competition.平衡肌动蛋白网络竞争中的有限资源。
Curr Biol. 2025 Feb 3;35(3):500-513.e5. doi: 10.1016/j.cub.2024.11.067. Epub 2025 Jan 9.
2
Self-organized spatial targeting of contractile actomyosin rings for synthetic cell division.肌动球蛋白收缩环的自组织空间靶向用于合成细胞分裂。
Nat Commun. 2024 Nov 29;15(1):10415. doi: 10.1038/s41467-024-54807-9.
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Mechanical power is maximized during contractile ring-like formation in a biomimetic dividing cell model.在仿生分裂细胞模型中,在收缩环样形成期间实现了机械功率的最大化。
Nat Commun. 2024 Nov 10;15(1):9731. doi: 10.1038/s41467-024-53228-y.
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Dynamic shape-shifting of the single-celled eukaryotic predator Lacrymaria via unconventional cytoskeletal components.通过非常规细胞骨架成分实现单细胞真核捕食者泪液生物的动态变形。
Curr Biol. 2024 Nov 4;34(21):4869-4883.e6. doi: 10.1016/j.cub.2024.09.003. Epub 2024 Sep 30.
5
Myosin-I synergizes with Arp2/3 complex to enhance the pushing forces of branched actin networks.肌球蛋白-I 与 Arp2/3 复合物协同作用以增强分支肌动蛋白网络的推力。
Sci Adv. 2024 Sep 13;10(37):eado5788. doi: 10.1126/sciadv.ado5788.
6
Phalloidin and DNase I-bound F-actin pointed end structures reveal principles of filament stabilization and disassembly.鬼笔环肽和 DNase I 结合的 F-肌动蛋白末端结构揭示了纤维稳定和拆卸的原理。
Nat Commun. 2024 Sep 11;15(1):7969. doi: 10.1038/s41467-024-52251-3.
7
Actin network evolution as a key driver of eukaryotic diversification.肌动蛋白网络进化作为真核生物多样化的关键驱动力。
J Cell Sci. 2024 Aug 1;137(15). doi: 10.1242/jcs.261660. Epub 2024 Aug 9.
8
Follow the flow: Actin and membrane act as an integrated system to globally coordinate cell shape and movement.追随流动:肌动蛋白和膜作为一个集成系统,全面协调细胞的形状和运动。
Curr Opin Cell Biol. 2024 Aug;89:102392. doi: 10.1016/j.ceb.2024.102392. Epub 2024 Jul 10.
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Mechanisms of actin filament severing and elongation by formins.formin 介导的肌动蛋白丝的截断和延伸机制。
Nature. 2024 Aug;632(8024):437-442. doi: 10.1038/s41586-024-07637-0. Epub 2024 Jun 6.
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F-actin architecture determines the conversion of chemical energy into mechanical work.F-肌动蛋白结构决定了化学能向机械功的转化。
Nat Commun. 2024 Apr 24;15(1):3444. doi: 10.1038/s41467-024-47593-x.