Department of Biochemistry and Molecular Biophysics, Howard Hughes Medical Institute, Columbia University, New York, NY 10032, USA.
Proc Natl Acad Sci U S A. 2010 Oct 12;107(41):17592-7. doi: 10.1073/pnas.1011247107. Epub 2010 Sep 27.
Intercellullar junctions formed by cadherins, including desmosomes and adherens junctions, comprise two dimensional arrays of "trans" dimers formed between monomers emanating from opposing cell surfaces. Lateral "cis" interfaces between cadherins from the same cell surface have been proposed to play a role in cadherin clustering. Although the molecular details of cis interactions remain uncertain, they must define an anisotropic arrangement where binding is favorable only in certain orientations. Here we report Monte Carlo simulations performed on a 2D lattice constructed to account for the anisotropy in cadherin cis interactions. A crucial finding is that the "phase transition" between freely diffusing cadherin monomers and dimers and a condensed ordered 2D junction formed by dimers alone is a cooperative process involving both trans and cis interactions. Moreover, cis interactions, despite being too weak to be measured in solution, are critical to the formation of an ordered junction structure. We discuss these results in light of available experimental information on cadherin binding free energies that are transformed from their bulk solution values to interaction energies on a 2D lattice.
细胞间连接由钙黏蛋白形成,包括桥粒和黏着连接,由来自对向细胞表面的单体发出的“跨”二聚体组成二维阵列。有人提出,同一细胞表面的钙黏蛋白之间的横向“顺式”界面在钙黏蛋白聚类中发挥作用。尽管顺式相互作用的分子细节仍不确定,但它们必须定义一种各向异性的排列,其中结合仅在某些方向上有利。在这里,我们报告了在二维晶格上进行的蒙特卡罗模拟,该晶格的构建考虑了钙黏蛋白顺式相互作用的各向异性。一个关键的发现是,自由扩散的钙黏蛋白单体和二聚体与仅由二聚体形成的有序 2D 连接之间的“相变”是一个涉及跨和顺式相互作用的协同过程。此外,尽管顺式相互作用弱到无法在溶液中测量,但对于形成有序的连接结构至关重要。我们根据可用的实验信息讨论这些结果,这些信息将钙黏蛋白结合自由能从其体相溶液值转换为二维晶格上的相互作用能。