Adelard Institute, Manchester M29 7FZ, UK.
Open Biol. 2012 Jul;2(7):120088. doi: 10.1098/rsob.120088.
The year 2011 marked the half-centenary of the publication of what came to be known as the Anfinsen postulate, that the tertiary structure of a folded protein is prescribed fully by the sequence of its constituent amino acid residues. This postulate has become established as a credo, and, indeed, no contradictions seem to have been found to date. However, the experiments that led to this postulate were conducted on only a single protein, bovine ribonuclease A (RNAse). We conduct molecular dynamics (MD) simulations on this protein with the aim of mimicking this experiment as well as making the methodology available for use with basically any protein. There have been many attempts to model denaturation and refolding processes of globular proteins in silico using MD, but only a few examples where disulphide-bond containing proteins were studied. We took the view that if the reductive deactivation and oxidative reactivation processes of RNAse could be modelled in silico, this would provide valuable insights into the workings of the classical Anfinsen experiment.
2011 年标志着所谓 Anfinsen 假设发表五十周年,该假设认为折叠蛋白质的三级结构完全由其组成氨基酸残基的序列决定。这个假设已经成为了一种信条,事实上,迄今为止似乎还没有发现任何矛盾。然而,导致这个假设的实验只在一种蛋白质,牛核糖核酸酶 A(RNAse)上进行。我们对该蛋白质进行分子动力学(MD)模拟,旨在模拟该实验,并使该方法可用于基本上任何蛋白质。已经有许多使用 MD 对球状蛋白质的变性和复性过程进行计算机模拟的尝试,但只有少数含二硫键的蛋白质的研究。我们认为,如果可以在计算机上模拟 RNAse 的还原失活和氧化复活过程,这将为经典 Anfinsen 实验的工作原理提供有价值的见解。