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J Phys Chem B. 2024 Jun 27;128(25):5987-5994. doi: 10.1021/acs.jpcb.4c01385. Epub 2024 Jun 11.
2
Protein-membrane interactions: sensing and generating curvature.蛋白质-膜相互作用:感应和产生曲率。
Trends Biochem Sci. 2024 May;49(5):401-416. doi: 10.1016/j.tibs.2024.02.005. Epub 2024 Mar 19.
3
Plasma membrane nanodeformations promote actin polymerization through CIP4/CDC42 recruitment and regulate type II IFN signaling.质膜纳米变形通过募集 CIP4/CDC42 促进肌动蛋白聚合,并调节 II 型 IFN 信号。
Sci Adv. 2023 Dec 15;9(50):eade1660. doi: 10.1126/sciadv.ade1660. Epub 2023 Dec 13.
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Curved adhesions mediate cell attachment to soft matrix fibres in three dimensions.弯曲的黏附物介导细胞在三维空间中与软基质纤维的附着。
Nat Cell Biol. 2023 Oct;25(10):1453-1464. doi: 10.1038/s41556-023-01238-1. Epub 2023 Sep 28.
5
Molecular mechanism of GPCR spatial organization at the plasma membrane.GPCR 在质膜上空间组织的分子机制。
Nat Chem Biol. 2024 Feb;20(2):142-150. doi: 10.1038/s41589-023-01385-4. Epub 2023 Jul 17.
6
The ins and outs of membrane bending by intrinsically disordered proteins.无序蛋白质介导的膜弯曲的来龙去脉。
Sci Adv. 2023 Jul 7;9(27):eadg3485. doi: 10.1126/sciadv.adg3485.
7
A NanoCurvS platform for quantitative and multiplex analysis of curvature-sensing proteins.用于定量和多重分析曲率感应蛋白的 NanoCurvS 平台。
Biomater Sci. 2023 Jul 25;11(15):5205-5217. doi: 10.1039/d2bm01856j.
8
Nanotopography modulates intracellular excitable systems through cytoskeleton actuation.纳米形貌通过细胞骨架的驱动来调节细胞内的兴奋系统。
Proc Natl Acad Sci U S A. 2023 May 9;120(19):e2218906120. doi: 10.1073/pnas.2218906120. Epub 2023 May 1.
9
Steric pressure between glycosylated transmembrane proteins inhibits internalization by endocytosis.糖基化跨膜蛋白之间的空间位阻抑制了通过胞吞作用的内化。
Proc Natl Acad Sci U S A. 2023 Apr 11;120(15):e2215815120. doi: 10.1073/pnas.2215815120. Epub 2023 Apr 6.
10
Nanotopography reveals metabolites that maintain the immunomodulatory phenotype of mesenchymal stromal cells.纳米形貌揭示了维持间充质基质细胞免疫调节表型的代谢物。
Nat Commun. 2023 Feb 10;14(1):753. doi: 10.1038/s41467-023-36293-7.

纳米生物界面处的细胞信号传导:聚焦膜曲率

Cellular Signaling at the Nano-Bio Interface: Spotlighting Membrane Curvature.

作者信息

Lu Chih-Hao, Lee Christina E, Nakamoto Melissa L, Cui Bianxiao

机构信息

Department of Chemistry, Stanford University, Stanford, California, USA; email:

Wu-Tsai Neuroscience Institute and Sarafan ChEM-H Institute, Stanford University, Stanford, California, USA.

出版信息

Annu Rev Phys Chem. 2025 Apr;76(1):251-277. doi: 10.1146/annurev-physchem-090722-021151.

DOI:10.1146/annurev-physchem-090722-021151
PMID:40258240
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12043246/
Abstract

No longer viewed as a passive consequence of cellular activities, membrane curvature-the physical shape of the cell membrane-is now recognized as an active constituent of biological processes. Nanoscale topographies on extracellular matrices or substrate surfaces impart well-defined membrane curvatures on the plasma membrane. This review examines biological events occurring at the nano-bio interface, the physical interface between the cell membrane and surface nanotopography, which activates intracellular signaling by recruiting curvature-sensing proteins. We encompass a wide range of biological processes at the nano-bio interface, including cell adhesion, endocytosis, glycocalyx redistribution, regulation of mechanosensitive ion channels, cell migration, and differentiation. Despite the diversity of processes, we call attention to the critical role of membrane curvature in each process. We particularly highlight studies that elucidate molecular mechanisms involving curvature-sensing proteins with the hope of providing comprehensive insights into this rapidly advancing area of research.

摘要

细胞膜曲率——细胞膜的物理形状——不再被视为细胞活动的被动结果,现在被认为是生物过程的一个活跃组成部分。细胞外基质或底物表面的纳米级形貌在质膜上赋予明确的膜曲率。本综述研究了在纳米-生物界面发生的生物事件,即细胞膜与表面纳米形貌之间的物理界面,该界面通过招募曲率感知蛋白激活细胞内信号传导。我们涵盖了纳米-生物界面的广泛生物过程,包括细胞粘附、内吞作用、糖萼再分布、机械敏感离子通道的调节、细胞迁移和分化。尽管过程多样,但我们提请注意膜曲率在每个过程中的关键作用。我们特别强调阐明涉及曲率感知蛋白分子机制的研究,希望能对这个快速发展的研究领域提供全面的见解。