Zooming across the Alchemical Space
Alchemical transformations, whereby chemical species are modified seamlessly, represent a powerful tool in molecular simulations and free-energy calculations, with a broad range of applications. A general-extent, or alchemical parameter, λ ∈ [0,1], describes the gradual transition between the initial and final states of the transformation, and its discretization critically affects the reliability and efficiency of the free-energy calculations. For transformations involving large moieties, free-energy perturbation (FEP) and thermodynamic integration (TI) require numerous intermediates, or λ-states, to ensure appropriate overlap of the configurational ensembles and suitable convergence of the simulation, each state demanding extensive sampling, which burdens computational feasibility. To address this limitation, we combine λ-dynamics─treating λ as a dynamic variable─with the enhanced-sampling approach well-tempered metadynamics-extended adaptive biasing force (WTM-eABF), forming the basis of WTM-λABF. By handling λ as a continuously varying collective variable (CV) and applying a bin-discretized bias, WTM-λABF efficiently explores the λ-space, even when the latter is stratified in numerous intermediates. Calculations of free-energies of hydration, of protein-ligand binding, and of amino-acid mutations in proteins reveal that WTM-λABF consistently converges faster than standard FEP or λ-ABF, with its advantages becoming more pronounced as the number of intermediates rises. We find that WTM-λABF can handle alchemical transformations efficiently with as many as 1,000 intermediates, allowing transformations involving large moieties, or significant potential-energy changes, to be tackled with utmost accuracy. Additionally, its rapid exploration of the continuous λ-space accelerates sampling in the orthogonal space. We are confident that WTM-λABF has the potential to serve as a foundational method for routine applications relevant to chemistry and biophysics, ranging from drug discovery to protein engineering and design.
Authors
- Wensheng Cai (ORCID: https://orcid.org/0000-0002-6457-7058)
- Haohao Fu (ORCID: https://orcid.org/0000-0003-0908-0046)
- Christophe J. Chipot (ORCID: https://orcid.org/0000-0002-9122-1698)
- Mengchen Zhou
- Xueguang Shao (ORCID: https://orcid.org/0000-0001-5027-4382)
Institutions
- University of Illinois Urbana-Champaign (US)
- Nankai University (CN)
- University of Chicago (US)
- Division of Materials Science and Engineering (AU)
- Unité Matériaux et Transformations (FR)
- Université de Lorraine (FR)
Publication Details
- Journal
- The Journal of Physical Chemistry Letters
- Published
- 2025-04-24
- DOI
- https://doi.org/10.1021/acs.jpclett.5c00525
- Citations
- 7
- Primary Topic
- Protein Structure and Dynamics
- Type
- article
- Field-Weighted Citation Impact
- 5.64