Bahadur R P, Zacharias M
School of Engineering and Science, Jacobs University Bremen, Bremen, Germany.
Cell Mol Life Sci. 2008 Apr;65(7-8):1059-72. doi: 10.1007/s00018-007-7451-x.
Specific protein-protein interactions are essential for cellular functions. Experimentally determined three-dimensional structures of protein-protein complexes offer the possibility to characterize binding interfaces in terms of size, shape and packing density. Comparison with crystal-packing interfaces representing nonspecific protein-protein contacts gives insight into how specific binding differs from nonspecific low-affinity binding. An overview is given on empirical structural rules for specific protein-protein recognition derived from known complex structures. Although single parameters such as interface size, shape or surface complementary show clear trends for different interface types, each parameter alone is insufficient to fully distinguish between specific versus crystal-packing contacts. A combination of interface parameters is, however, well suited to characterize a specific interface. This knowledge provides us with the essential ingredients that make up a specific protein recognition site. It is also of great value for the prediction of protein binding sites and for the evaluation of predicted complex structures.
特定的蛋白质 - 蛋白质相互作用对于细胞功能至关重要。通过实验测定的蛋白质 - 蛋白质复合物的三维结构,为从大小、形状和堆积密度等方面表征结合界面提供了可能性。与代表非特异性蛋白质 - 蛋白质接触的晶体堆积界面进行比较,有助于深入了解特异性结合与非特异性低亲和力结合的差异。本文概述了从已知复合物结构中得出的特异性蛋白质 - 蛋白质识别的经验结构规则。尽管诸如界面大小、形状或表面互补性等单个参数对于不同的界面类型呈现出明显的趋势,但仅靠每个参数都不足以完全区分特异性接触与晶体堆积接触。然而,界面参数的组合非常适合表征特定的界面。这些知识为我们提供了构成特定蛋白质识别位点的基本要素。它对于预测蛋白质结合位点以及评估预测的复合物结构也具有重要价值。