Bell G I
Cell Biophys. 1979 Jun;1(2):133-47. doi: 10.1007/BF02781347.
A theoretical model is developed for cell-to-cell binding by bivalent ligands that can bind to mobile receptors on the cell surfaces. Monovalent inhibitors that can bind either to receptors or ligands are also included. For symmetrical ligands, that is, ligands in which both binding sites are the same, it is shown that crosslinking of receptors on each cell will interfere with intercellular bridge formation. At equilibrium, such interference is not drastic, but if the crosslinks can form before the cells are brought into contact, crosslinking may greatly impede the rate of intercellular binding. Comparison is made with experiments, and the importance of receptor mobility is discussed. It is noted that ligands can also bind a cell to itself or to a surface.
建立了一个理论模型,用于研究双价配体与细胞表面可移动受体之间的细胞间结合。还包括可与受体或配体结合的单价抑制剂。对于对称配体,即两个结合位点相同的配体,研究表明每个细胞上受体的交联会干扰细胞间桥的形成。在平衡状态下,这种干扰并不剧烈,但如果在细胞接触之前就能形成交联,交联可能会极大地阻碍细胞间结合的速率。与实验进行了比较,并讨论了受体流动性的重要性。需要注意的是,配体也可以使细胞自身或细胞与表面结合。