Yang Ye, Lyubartsev Alexander P, Korolev Nikolay, Nordenskiöld Lars
School of Biological Sciences, Nanyang Technological University, Singapore.
Biophys J. 2009 Mar 18;96(6):2082-94. doi: 10.1016/j.bpj.2008.10.073.
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 (Mg(2+)), 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 Mg(2+). Simulations for systems with a gradual substitution of K(+) for Mg(2+), to mimic the Mg(2+) titration of an NCP solution, were performed. The rNCP system showed stronger aggregation that occurred at lower concentrations of added Mg(2+), 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.
针对模拟核小体核心颗粒(NCP)溶液的系统进行了粗粒度朗之万分子动力学计算机模拟。NCP被建模为一个带负电荷的球形颗粒,代表DNA与组蛋白球状部分的复合物,并结合了模拟组蛋白尾巴的连接带电珠子串。尾巴相对于核心的大小、电荷和分布构建得与真实的NCP相匹配。构建了三种NCP模型来代表组蛋白尾巴上不同程度的共价修饰:(未修饰的)重组体(rNCP)、乙酰化的(aNCP)以及乙酰化和磷酸化的(paNCP)。模拟单元在具有明确移动抗衡离子和添加盐的介电连续介质中包含10个NCP。NCP - NCP相互作用决定性地取决于组蛋白尾巴的修饰状态和盐条件。将单价盐浓度(KCl)从无盐增加到生理浓度会导致rNCP在溶液中发生NCP聚集,而在aNCP系统中仅偶尔观察到NCP缔合。在存在二价盐(Mg(2+))的情况下,rNCP形成致密稳定的聚集体,而aNCP形成聚集体的频率较低。聚集体通过组蛋白尾巴桥接和抗衡离子在NCP - NCP接触区域的积累而形成。添加KCl时或存在Mg(2+)时,paNCP不显示NCP - NCP相互作用。进行了用Mg(2+)逐渐替代K(+)的系统模拟,以模拟NCP溶液的Mg(2+)滴定。与aNCP系统相比,rNCP系统在添加较低浓度的Mg(2+)时显示出更强的聚集。在模拟单元中对单个NCP进行的额外分子动力学模拟表明,在广泛的盐浓度范围内,尾巴与NCP核心的分离程度适中。这意味着盐诱导的组蛋白尾巴与球状NCP的解离本身并不是NCP - NCP聚集的主要因素。在对照模拟中测试了将NCP描述为具有均匀电荷分布的球体的粗粒度近似。对NCP更详细的描述并没有改变结果的主要特征。总体而言,这项工作的结果与报道的NCP溶液和染色质阵列的实验数据一致。