School of Physics, Huazhong University of Science and Technology, Wuhan 430074, China.
Int J Mol Sci. 2019 Jul 6;20(13):3325. doi: 10.3390/ijms20133325.
The recruitment and transference of proteins through protein-protein interactions is a general process involved in various biological functions in cells. Despite the importance of this general process, the dynamic mechanism of how proteins are recruited and transferred from one interacting partner to another remains unclear. In this study, we investigated the dynamic mechanisms of recruitment and translocation of histone chaperone CIA/ASF1 for nucleosome disassembly by exploring the conformational space and the free energy profile of unbound DBD(CCG1) and CIA/ASF1-bound DBD(CCG1) systems through extensive molecular dynamics simulations. It was found that there exists three metastable conformational states for DBD(CCG1), an unbound closed state, a CIA/ASF1-bound half-open state, and an open state. The free energy landscape shows that the closed state and the half-open state are separated by a high free energy barrier, while the half-open state and the open state are connected with a moderate free energy increase. The high free energy barrier between the closed and half-open states explains why DBD(CCG1) can recruit CIA/ASF1 and remain in the binding state during the transportation. In addition, the asymmetric binding of CIA/ASF1 on DBD(CCG1) allows DBD(CCG1) to adopt the open state by moving one of its two domains, such that the exposed domain of DBD(CCG1) is able to recognize the acetylated histone H4 tails. As such, CIA/ASF1 has a chance to translocate from DBD(CCG1) to histone, which is also facilitated by the moderate energy increase from the bound half-open state to the open state of DBD(CCG1). These findings suggest that the recruitment and transference of histone chaperone CIA/ASF1 is highly favored by its interaction with DBD(CCG1) via conformational selection and asymmetric binding, which may represent a general mechanism of similar biological processes.
蛋白质通过蛋白质-蛋白质相互作用的募集和转移是细胞中各种生物功能涉及的普遍过程。尽管这个普遍过程很重要,但蛋白质从一个相互作用的伙伴招募和转移到另一个伙伴的动态机制仍不清楚。在这项研究中,我们通过广泛的分子动力学模拟,研究了组蛋白伴侣 CIA/ASF1 募集和易位到核小体解组装的动态机制,探索了未结合 DBD(CCG1)和 CIA/ASF1 结合 DBD(CCG1)系统的构象空间和自由能分布。结果发现,DBD(CCG1)存在三种亚稳态构象状态,即无结合的闭合状态、CIA/ASF1 结合的半开状态和开放状态。自由能景观表明,闭合状态和半开状态之间存在一个高自由能势垒,而半开状态和开放状态之间则通过中等自由能增加相连接。闭合状态和半开状态之间的高自由能势垒解释了为什么 DBD(CCG1)能够招募 CIA/ASF1 并在运输过程中保持结合状态。此外,CIA/ASF1 对 DBD(CCG1)的不对称结合允许 DBD(CCG1)通过移动其两个结构域之一来采用开放状态,从而使 DBD(CCG1)的暴露结构域能够识别乙酰化组蛋白 H4 尾巴。因此,CIA/ASF1 有机会从 DBD(CCG1)易位到组蛋白,这也得益于从结合的半开状态到 DBD(CCG1)的开放状态的中等能量增加。这些发现表明,组蛋白伴侣 CIA/ASF1 的募集和转移通过构象选择和不对称结合与 DBD(CCG1)相互作用高度有利,这可能代表了类似生物过程的一般机制。