Langini Cassiano, Caflisch Amedeo, Vitalis Andreas
From the Department of Biochemistry, University of Zurich, CH-8057 Zurich, Switzerland.
From the Department of Biochemistry, University of Zurich, CH-8057 Zurich, Switzerland
J Biol Chem. 2017 Oct 6;292(40):16734-16745. doi: 10.1074/jbc.M117.786350. Epub 2017 Aug 10.
Bromodomains are protein modules adopting conserved helix bundle folds. Some bromodomain-containing proteins, such as ATPase family AAA domain-containing protein 2 (ATAD2), isoform A, have attracted much interest because they are overexpressed in many types of cancer. Bromodomains bind to acetylated lysine residues on histone tails and thereby facilitate the reading of the histone code. Epigenetic regulators in general have been implicated as indicators, mediators, or causes of a large number of diseases and disorders. To interfere with or modulate these processes, it is therefore of fundamental interest to understand the molecular mechanisms by which epigenetic regulation occurs. Here, we present results from molecular dynamics simulations of a doubly acetylated histone H4 peptide bound to the bromodomain of ATAD2 (hereafter referred to as ATAD2A). These simulations revealed how the flexibility of ATAD2A's major loop, the so-called ZA loop, creates an adaptable interface that preserves the disorder of both peptide and loop in the bound state. We further demonstrate that the binding involves an almost identical average pattern of interactions irrespective of which acetyl mark is inserted into the pocket. In conjunction with a likely mechanism of electrostatically driven recruitment, our simulation results highlight how the bromodomain is built toward promiscuous binding with low specificity. In conclusion, the simulations indicate that disorder and electrostatic steering function jointly to recruit ATAD2A to the histone core and that these fuzzy interactions may promote cooperativity between nearby epigenetic marks.
溴结构域是具有保守螺旋束折叠的蛋白质模块。一些含溴结构域的蛋白质,如含ATP酶家族AAA结构域蛋白2(ATAD2)的A亚型,因其在多种癌症中过度表达而备受关注。溴结构域与组蛋白尾部的乙酰化赖氨酸残基结合,从而有助于解读组蛋白密码。一般来说,表观遗传调节因子被认为是大量疾病和紊乱的指标、介质或病因。为了干扰或调节这些过程,因此了解表观遗传调控发生的分子机制具有根本重要性。在此,我们展示了与ATAD2的溴结构域(以下简称ATAD2A)结合的双乙酰化组蛋白H4肽的分子动力学模拟结果。这些模拟揭示了ATAD2A主要环(即所谓的ZA环)的灵活性如何创建一个适应性界面,该界面在结合状态下保持肽和环的无序性。我们进一步证明,无论哪个乙酰标记插入口袋中,结合都涉及几乎相同的平均相互作用模式。结合静电驱动招募的可能机制,我们的模拟结果突出了溴结构域如何朝着低特异性的混杂结合构建。总之,模拟表明无序和静电引导共同作用将ATAD2A招募到组蛋白核心,并且这些模糊相互作用可能促进附近表观遗传标记之间的协同作用。