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钙黏蛋白黏附的机制与动力学

Mechanism and dynamics of cadherin adhesion.

作者信息

Leckband Deborah, Prakasam Anil

机构信息

Department of Chemical Engineering, University of Illinois at Urbana-Champaign, Urbana-Champaign, Illinois 61801, USA.

出版信息

Annu Rev Biomed Eng. 2006;8:259-87. doi: 10.1146/annurev.bioeng.8.061505.095753.

DOI:10.1146/annurev.bioeng.8.061505.095753
PMID:16834557
Abstract

Cadherins are essential cell adhesion molecules involved in tissue morphogenesis and the maintenance of tissue architecture in adults. The adhesion and selectivity functions of cadherins are located in their extracellular regions. Biophysical studies show that the adhesive activity is not confined to a single interface. Instead, multiple cadherin domains contribute to binding. By contrast, the specificity-determining site maps to the N-terminal domains, which adhere by the reciprocal binding of Trp2 residues from opposing proteins. Structural cooperativity can transmit the effects of subtle structural changes or ligand binding over large distances in the protein. Increasingly, studies show that differential cadherin-mediated adhesion, rather than exclusive homophilic binding between identical cadherins, direct cell segregation and the organization of tissue interfaces during morphogenesis. Force measurements quantified both kinetic and strength differences between different classical cadherins that may underlie cell sorting behavior. Despite the complex adhesion mechanisms and differences in binding properties, cadherin-mediated cell adhesion is also regulated by many other biochemical processes. Elucidating the mechanisms by which cadherins organize cell junctions and tissue architecture requires not only quantitative, mechanistic investigations of cadherin function but also investigations of the biochemical and cellular processes that can modulate those functions.

摘要

钙黏蛋白是参与组织形态发生和维持成体组织结构的重要细胞黏附分子。钙黏蛋白的黏附及选择性功能位于其细胞外区域。生物物理学研究表明,黏附活性并不局限于单一界面。相反,多个钙黏蛋白结构域都参与结合。相比之下,特异性决定位点定位于N端结构域,其通过来自相对蛋白的Trp2残基的相互结合而黏附。结构协同性可在蛋白质中远距离传递细微结构变化或配体结合的效应。越来越多的研究表明,在形态发生过程中,不同钙黏蛋白介导的黏附作用,而非相同钙黏蛋白之间排他性的嗜同性结合,指导细胞分离和组织界面的组织形成。力测量量化了不同经典钙黏蛋白之间的动力学和强度差异,这些差异可能是细胞分选行为的基础。尽管存在复杂的黏附机制和结合特性差异,但钙黏蛋白介导的细胞黏附也受到许多其他生化过程的调控。阐明钙黏蛋白组织细胞连接和组织结构的机制,不仅需要对钙黏蛋白功能进行定量的、机械学的研究,还需要研究能够调节这些功能的生化和细胞过程。

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