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采用坐标交换的炼金术转移方法对同系配体和大分子突变体进行相对结合自由能估计。

Relative Binding Free Energy Estimation of Congeneric Ligands and Macromolecular Mutants with the Alchemical Transfer Method with Coordinate Swapping.

作者信息

Gallicchio Emilio

机构信息

Department of Chemistry and Biochemistry, Brooklyn College of the City University of New York, New York, New York 11210, United States.

Ph.D. Program in Chemistry, The Graduate Center of the City University of New York, New York, New York 10016, United States.

出版信息

J Chem Inf Model. 2025 Apr 14;65(7):3706-3714. doi: 10.1021/acs.jcim.5c00207. Epub 2025 Mar 26.

Abstract

We present the Alchemical Transfer with Coordinate Swapping (ATS) method to enable the calculation of the relative binding free energies between large congeneric ligands and single-point mutant peptides to protein receptors with the Alchemical Transfer Method (ATM) framework. Similarly to ATM, the new method implements the alchemical transformation as a coordinate transformation and works with any unmodified force fields and standard chemical topologies. Unlike ATM, which transfers whole ligands in and out of the receptor binding site, ATS limits the magnitude of the alchemical perturbation by transferring only the portion of the molecules that differ between the bound and unbound ligands. The common region of the two ligands, which can be arbitrarily large, is unchanged and does not contribute to the magnitude and statistical fluctuations of the perturbation energy. Internally, the coordinates of the atoms of the common regions are swapped to maintain the integrity of the covalent bonding data structures of the OpenMM molecular dynamics engine. The work successfully validates the method on protein-ligand and protein-peptide RBFE benchmarks. This advance paves the road for the application of the relative binding free energy Alchemical Transfer Method protocol to study the effect of protein and nucleic acid mutations on the binding affinity and specificity of macromolecular complexes.

摘要

我们提出了一种带坐标交换的炼金术转移(ATS)方法,以便在炼金术转移方法(ATM)框架下计算大型同类配体与蛋白质受体单点突变肽之间的相对结合自由能。与ATM类似,新方法将炼金术转化实现为坐标变换,并适用于任何未修改的力场和标准化学拓扑结构。与ATM不同,ATM是将整个配体移入和移出受体结合位点,而ATS仅转移结合态和未结合态配体之间不同的分子部分,从而限制了炼金术微扰的幅度。两个配体的公共区域可以任意大,保持不变,且对微扰能量的幅度和统计波动没有贡献。在内部,交换公共区域原子的坐标,以维持OpenMM分子动力学引擎共价键数据结构的完整性。这项工作成功地在蛋白质-配体和蛋白质-肽相对结合自由能基准测试中验证了该方法。这一进展为应用相对结合自由能炼金术转移方法协议来研究蛋白质和核酸突变对大分子复合物结合亲和力和特异性的影响铺平了道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3910/12004517/87b3981aa224/ci5c00207_0001.jpg

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