Leckband Deborah, Sivasankar Sanjeevi
Department of Chemistry, Department of Chemical and Biomolecular Engineering, Center for Biophysics and Computational Biology, University of Illinois at Urbana-Champaign, 600 South Mathews Ave, 61801, Urbana, IL, USA,
Subcell Biochem. 2012;60:63-88. doi: 10.1007/978-94-007-4186-7_4.
Since the identification of cadherins and the publication of the first crystal structures, the mechanism of cadherin adhesion, and the underlying structural basis have been studied with a number of different experimental techniques, different classical cadherin subtypes, and cadherin fragments. Earlier studies based on biophysical measurements and structure determinations resulted in seemingly contradictory findings regarding cadherin adhesion. However, recent experimental data increasingly reveal parallels between structures, solution binding data, and adhesion-based biophysical measurements that are beginning to both reconcile apparent differences and generate a more comprehensive model of cadherin-mediated cell adhesion. This chapter summarizes the functional, structural, and biophysical findings relevant to cadherin junction assembly and adhesion. We emphasize emerging parallels between findings obtained with different experimental approaches. Although none of the current models accounts for all of the available experimental and structural data, this chapter discusses possible origins of apparent discrepancies, highlights remaining gaps in current knowledge, and proposes challenges for further study.
自从钙黏蛋白被鉴定出来以及首个晶体结构公布以来,人们运用多种不同的实验技术、不同的经典钙黏蛋白亚型和钙黏蛋白片段,对钙黏蛋白的黏附机制及其潜在的结构基础进行了研究。早期基于生物物理测量和结构测定的研究,在钙黏蛋白黏附方面得出了看似相互矛盾的结果。然而,最近的实验数据越来越多地揭示了结构、溶液结合数据和基于黏附的生物物理测量之间的相似之处,这些相似之处开始既调和了明显的差异,又生成了一个更全面的钙黏蛋白介导的细胞黏附模型。本章总结了与钙黏蛋白连接组装和黏附相关的功能、结构和生物物理研究结果。我们强调了通过不同实验方法获得的研究结果之间新出现的相似之处。尽管目前没有一个模型能够解释所有现有的实验和结构数据,但本章讨论了明显差异可能的来源,突出了当前知识中仍然存在的空白,并提出了进一步研究的挑战。