Laracuente Xavier E, Delfing Bryan M, Luo Xingyu, Olson Audrey, Jeffries William, Bowers Steven R, Foreman Kenneth W, Lee Kyung Hyeon, Paige Mikell, Kehn-Hall Kylene, Lockhart Christopher, Klimov Dmitri K
School of Systems Biology, George Mason University, Manassas, Virginia 20110, United States.
Department of Chemistry and Biochemistry, George Mason University, Fairfax, Virginia 22030, United States.
J Chem Theory Comput. 2025 Apr 22;21(8):4286-4298. doi: 10.1021/acs.jctc.5c00121. Epub 2025 Apr 6.
We have developed and tested an absolute free energy perturbation (FEP) protocol, which combines all-atom molecular dynamics, replica exchange with solute tempering (REST) enhanced sampling, and a spherical harmonic restraint applied to a ligand. Our objective was to compute the binding free energy together with the underlying binding mechanism for a ligand, which binds diffusively to a protein. Such ligands represent nearly impossible targets for traditional FEP simulations. To test our FEP/REST protocol, we selected a conserved motif peptide KKPK termed minNLS from the nuclear localization signal sequence of the Venezuelan equine encephalitis virus capsid protein. This peptide fragment binds diffusively to importin-α transport protein without forming well-defined poses. Our FEP/REST simulations with a spherical restraint provided a converged estimate of minNLS binding free energy. We found that minNLS binds with moderate affinity to importin-α utilizing an unusual, purely entropic mechanism in which binding free energy is determined by favorable entropic gain. For this cationic minNLS peptide, a favorable binding entropic gain is primarily associated with the release of water from the solvation shells of charged amino acids. We demonstrated that FEP/REST simulations sample the KKPK bound ensemble well, allowing us to characterize the distribution of bound structures, binding interactions, and locations on the importin-α surface. Analysis of experimental studies offered support to our rationale behind the KKPK entropic binding mechanism.
我们已经开发并测试了一种绝对自由能微扰(FEP)方案,该方案结合了全原子分子动力学、溶质回火复制交换(REST)增强采样以及应用于配体的球谐约束。我们的目标是计算一种配体的结合自由能及其潜在的结合机制,该配体以扩散方式与蛋白质结合。对于传统的FEP模拟来说,这类配体几乎是不可能的目标。为了测试我们的FEP/REST方案,我们从委内瑞拉马脑炎病毒衣壳蛋白的核定位信号序列中选择了一个保守基序肽KKPK,称为minNLS。该肽片段以扩散方式与输入蛋白-α转运蛋白结合,未形成明确的构象。我们使用球形约束进行的FEP/REST模拟提供了minNLS结合自由能的收敛估计。我们发现,minNLS以中等亲和力与输入蛋白-α结合,利用一种不寻常的、纯粹的熵机制,其中结合自由能由有利的熵增决定。对于这种阳离子minNLS肽,有利的结合熵增主要与带电氨基酸溶剂化壳层中的水释放有关。我们证明,FEP/REST模拟很好地采样了KKPK结合系综,使我们能够表征结合结构的分布、结合相互作用以及在输入蛋白-α表面的位置。实验研究分析为我们关于KKPK熵结合机制的基本原理提供了支持。