Owen Gethin R, Stokes David L
New York Structural Biology Center, 89 Convent Avenue, New York, NY 10027, USA.
Dermatol Res Pract. 2010;2010:930401. doi: 10.1155/2010/930401. Epub 2010 Jun 21.
Desmosomes are a complex assembly of protein molecules that mediate adhesion between adjacent cells. Desmosome composition is well established and spatial relationships between components have been identified. Intercellular cell-cell adhesion is created by the interaction of extracellular domains of desmosomal cadherins, namely, desmocollins and desmogleins. High-resolution methods have provided insight into the structural interactions between cadherins. However, there is a lack of understanding about the architecture of the intact desmosomes and the physical principles behind their adhesive strength are unclear. Electron Tomography (ET) studies have offered three-dimensional visual data of desmosomal cadherin associations at molecular resolution. This review discusses the merits of two cadherin association models represented using ET. We discuss the possible role of sample preparation on the structural differences seen between models and the possibility of adaptive changes in the structure as a direct consequence of mechanical stress and stratification.
桥粒是介导相邻细胞间黏附的蛋白质分子的复杂集合体。桥粒的组成已明确,各组分间的空间关系也已确定。细胞间的黏附是由桥粒钙黏蛋白(即桥粒芯蛋白和桥粒胶蛋白)的胞外结构域相互作用产生的。高分辨率方法为深入了解钙黏蛋白之间的结构相互作用提供了依据。然而,人们对完整桥粒的结构缺乏了解,其黏附强度背后的物理原理也不清楚。电子断层扫描(ET)研究已在分子分辨率下提供了桥粒钙黏蛋白缔合的三维可视化数据。本综述讨论了用ET呈现的两种钙黏蛋白缔合模型的优点。我们讨论了样品制备对模型间结构差异的可能影响,以及结构因机械应力和分层而直接产生适应性变化的可能性。