Yantai Yuhuangding Hospital, Yantai, Shandong Province 264000, China.
FEBS Lett. 2013 Jan 16;587(2):136-41. doi: 10.1016/j.febslet.2012.11.001. Epub 2012 Nov 21.
Coevolution between proteins is crucial for understanding protein-protein interaction. Simultaneous changes allow a protein complex to maintain its overall structural-functional integrity. In this study, we combined statistical coupling analysis (SCA) and molecular dynamics simulations on the CDK6-CDKN2A protein complex to evaluate coevolution between proteins. We reconstructed an inter-protein residue coevolution network, consisting of 37 residues and 37 interactions. It shows that most of the coevolved residue pairs are spatially proximal. When the mutations happened, the stable local structures were broken up and thus the protein interaction was decreased or inhibited, with a following increased risk of melanoma. The identification of inter-protein coevolved residues in the CDK6-CDKN2A complex can be helpful for designing protein engineering experiments.
蛋白质之间的共进化对于理解蛋白质-蛋白质相互作用至关重要。同时发生的变化可以使蛋白质复合物保持其整体结构-功能的完整性。在这项研究中,我们结合了统计耦合分析(SCA)和分子动力学模拟,对 CDK6-CDKN2A 蛋白质复合物进行了研究,以评估蛋白质之间的共进化。我们重建了一个蛋白质间残基共进化网络,由 37 个残基和 37 个相互作用组成。结果表明,大多数共进化的残基对在空间上是接近的。当发生突变时,稳定的局部结构被打破,从而导致蛋白质相互作用减少或抑制,黑色素瘤的风险增加。鉴定 CDK6-CDKN2A 复合物中蛋白质间的共进化残基有助于设计蛋白质工程实验。