Theoretical Sciences Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Bangalore-560064, India.
PLoS One. 2018 Jun 13;13(6):e0198645. doi: 10.1371/journal.pone.0198645. eCollection 2018.
Amino acid mutations in proteins are random and those mutations which are beneficial or neutral survive during the course of evolution. Conservation or co-evolution analyses are performed on the multiple sequence alignment of homologous proteins to understand how important different amino acids or groups of them are. However, these traditional analyses do not explore the directed influence of amino acid mutations, such as compensatory effects. In this work we develop a method to capture the directed evolutionary impact of one amino acid on all other amino acids, and provide a visual network representation for it. The method developed for these directed networks of inter- and intra-protein evolutionary interactions can also be used for noting the differences in amino acid evolution between the control and experimental groups. The analysis is illustrated with a few examples, where the method identifies several directed interactions of functionally critical amino acids. The impact of an amino acid is quantified as the number of amino acids that are influenced as a consequence of its mutation, and it is intended to summarize the compensatory mutations in large evolutionary sequence data sets as well as to rationally identify targets for mutagenesis when their functional significance can not be assessed using structure or conservation.
蛋白质中的氨基酸突变是随机的,而在进化过程中那些有益或中性的突变得以存活。通过对同源蛋白的多序列比对进行保守性或共进化分析,可以了解不同氨基酸或氨基酸组的重要性。然而,这些传统的分析方法并没有探索氨基酸突变的定向影响,如补偿效应。在这项工作中,我们开发了一种方法来捕捉一个氨基酸对所有其他氨基酸的定向进化影响,并提供了一个可视化的网络表示。为这些蛋白质内和蛋白质间进化相互作用的有向网络开发的方法也可以用于记录对照组和实验组之间氨基酸进化的差异。通过一些例子来说明这种分析方法,其中该方法确定了几个功能关键氨基酸的有向相互作用。一个氨基酸的影响程度用其突变后受影响的氨基酸数量来量化,其目的是总结大型进化序列数据集的补偿突变,以及在无法使用结构或保守性评估其功能意义时,合理地确定诱变的靶标。