Li Lei, Zhao Bing, Cui Zhanhua, Gan Jacob, Sakharkar Meena Kishore, Kangueane Pandjassarame
School of mechanical and aerospace engineering, Nanyang Technological University, Singapore - 639798.
Bioinformation. 2006 Apr 4;1(4):121-6. doi: 10.6026/97320630001121.
It is known that binding free energy of protein-protein interaction is mainly contributed by hot spot (high energy) interface residues. Here, we investigate the characteristics of hot spots by examining inter-atomic sidechain-sidechain interactions using a dataset of 296 alanine-mutated interface residues. Results show that hot spots participate in strong and energetically favorable sidechain-sidechain interactions. Subsequently, we describe a novel, yet simple 'hot spot' prediction model with an accuracy that is similar to many available approaches. The model is also shown to efficiently distinguish specific protein-protein interactions from non-specific interactions.
已知蛋白质-蛋白质相互作用的结合自由能主要由热点(高能量)界面残基贡献。在此,我们通过使用296个丙氨酸突变的界面残基数据集检查原子间侧链-侧链相互作用来研究热点的特征。结果表明,热点参与强烈且能量有利的侧链-侧链相互作用。随后,我们描述了一种新颖但简单的“热点”预测模型,其准确性与许多现有方法相似。该模型还被证明能够有效地区分特异性蛋白质-蛋白质相互作用和非特异性相互作用。