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上皮顶端连接复合体的分级分离:对不同亚结构中蛋白质分布的重新评估。

Fractionation of the epithelial apical junctional complex: reassessment of protein distributions in different substructures.

作者信息

Vogelmann Roger, Nelson W James

机构信息

Department of Molecular and Cellular Physiology, Beckman Center for Molecular and Genetic Medicine, Stanford University School of Medicine, Stanford, CA 94305-5435, USA.

出版信息

Mol Biol Cell. 2005 Feb;16(2):701-16. doi: 10.1091/mbc.e04-09-0827. Epub 2004 Nov 17.

Abstract

The epithelial apical junctional complex (AJC) is an important regulator of cell structure and function. The AJC is compartmentalized into substructures comprising the tight and adherens junctions, and other membrane complexes containing the membrane proteins nectin, junctional adhesion molecule, and crumbs. In addition, many peripheral membrane proteins localize to the AJC. Studies of isolated proteins indicate a complex map of potential binding partners in which there is extensive overlap in the interactions between proteins in different AJC substructures. As an alternative to a direct search for specific protein-protein interactions, we sought to separate membrane substructures of the AJC in iodixanol density gradients and define their protein constituents. Results show that the AJC can be fractured into membrane substructures that contain specific membrane and peripheral membrane proteins. The composition of each substructure reveals a more limited overlap in common proteins than predicted from the inventory of potential interactions; some of the overlapping proteins may be involved in stepwise recruitment and assembly of AJC substructures.

摘要

上皮顶端连接复合体(AJC)是细胞结构和功能的重要调节因子。AJC被分隔成包含紧密连接和黏着连接的亚结构,以及其他含有膜蛋白nectin、连接黏附分子和crumbs的膜复合体。此外,许多外周膜蛋白定位于AJC。对分离蛋白的研究表明存在一个潜在结合伙伴的复杂图谱,其中不同AJC亚结构中的蛋白之间的相互作用存在广泛重叠。作为直接寻找特定蛋白质-蛋白质相互作用的替代方法,我们试图在碘克沙醇密度梯度中分离AJC的膜亚结构,并确定其蛋白质成分。结果表明,AJC可断裂成包含特定膜蛋白和外周膜蛋白的膜亚结构。每个亚结构的组成显示,共同蛋白的重叠比根据潜在相互作用清单预测的要有限;一些重叠蛋白可能参与AJC亚结构的逐步募集和组装。

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