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Computer Modeling Reveals that Modifications of the Histone Tail Charges Define Salt-Dependent Interaction of the Nucleosome Core Particles

机译:计算机建模表明组蛋白尾部电荷的修饰定义了核小体核心颗粒的盐依赖性相互作用

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摘要

Coarse-grained Langevin molecular dynamics computer simulations were conducted for systems that mimic solutions of nucleosome core particles (NCPs). The NCP was modeled as a negatively charged spherical particle representing the complex of DNA and the globular part of the histones combined with attached strings of connected charged beads modeling the histone tails. The size, charge, and distribution of the tails relative to the core were built to match real NCPs. Three models of NCPs were constructed to represent different extents of covalent modification on the histone tails: (nonmodified) recombinant (rNCP), acetylated (aNCP), and acetylated and phosphorylated (paNCP). The simulation cell contained 10 NCPs in a dielectric continuum with explicit mobile counterions and added salt. The NCP-NCP interaction is decisively dependent on the modification state of the histone tails and on salt conditions. Increasing the monovalent salt concentration (KCl) from salt-free to physiological concentration leads to NCP aggregation in solution for rNCP, whereas NCP associates are observed only occasionally in the system of aNCPs. In the presence of divalent salt (Mg2+), rNCPs form dense stable aggregates, whereas aNCPs form aggregates less frequently. Aggregates are formed via histone-tail bridging and accumulation of counterions in the regions of NCP-NCP contacts. The paNCPs do not show NCP-NCP interaction upon addition of KCl or in the presence of Mg2+. Simulations for systems with a gradual substitution of K+ for Mg2+, to mimic the Mg2+ titration of an NCP solution, were performed. The rNCP system showed stronger aggregation that occurred at lower concentrations of added Mg2+, compared to the aNCP system. Additional molecular dynamics simulations performed with a single NCP in the simulation cell showed that detachment of the tails from the NCP core was modest under a wide range of salt concentrations. This implies that salt-induced tail dissociation of the histone tails from the globular NCP is not in itself a major factor in NCP-NCP aggregation. The approximation of coarse-graining, with respect to the description of the NCP as a sphere with uniform charge distribution, was tested in control simulations. A more detailed description of the NCP did not change the main features of the results. Overall, the results of this work are in agreement with experimental data reported for NCP solutions and for chromatin arrays.
机译:对模拟核小体核心粒子(NCP)溶液的系统进行了粗粒度的Langevin分子动力学计算机模拟。 NCP被建模为带负电荷的球形颗粒,代表DNA与组蛋白的球状部分的复合物,并结合了连接的带电珠串,从而模拟了组蛋白尾巴。尾部相对于核心的大小,电荷和分布是为了匹配实际的NCP而建立的。构造了三种NCP模型来代表组蛋白尾巴上共价修饰的不同程度:(未修饰)重组(rNCP),乙酰化(aNCP),乙酰化和磷酸化(paNCP)。模拟单元在电介质连续体中包含10个NCP,具有明确的可移动抗衡离子和添加的盐。 NCP-NCP相互作用决定性地取决于组蛋白尾部的修饰状态和盐条件。将一价盐浓度(KCl)从无盐浓度增加到生理浓度会导致rNCP溶液中NCP聚集,而仅在aNCPs系统中偶尔观察到NCP缔合体。在存在二价盐(Mg 2 + )的情况下,rNCPs形成致密的稳定聚集体,而aNCPs形成聚集体的频率降低。通过在NCP-NCP接触区域中组蛋白尾桥和抗衡离子的积累形成聚集体。在加入KCl或存在Mg 2 + 的情况下,paNCP不会显示NCP-NCP相互作用。对用K + 逐渐替代Mg 2 + 来模拟NCP溶液的Mg 2 + 滴定的系统进行了模拟。与aNCP系统相比,rNCP系统显示出更强的聚集,发生在较低浓度的Mg 2 + 时。在模拟单元中使用单个NCP进行的其他分子动力学模拟表明,在宽范围的盐浓度下,尾部从NCP核心上的分离是适度的。这表明盐诱导的组蛋白尾巴从球状NCP的尾巴解离本身并不是NCP-NCP聚集的主要因素。在控制模拟中测试了相对于将NCP描述为具有均匀电荷分布的球体而言,粗粒度的近似值。对NCP的更详细描述并没有改变结果的主要特征。总的来说,这项工作的结果与针对NCP解决方案和染色质阵列报道的实验数据一致。

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