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

Institutions

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
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Zooming across the Alchemical Space

Wensheng Cai, Haohao Fu, Christophe J. Chipot, Mengchen Zhou et al.
7 citations
The Journal of Physical Chemistry Letters
Protein Structure and Dynamics
5.64
article

Zooming across the Alchemical Space

Wensheng Cai, Haohao Fu, Christophe J. Chipot, Mengchen Zhou, Xueguang Shao
article en
7 citations

Abstract

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.

The Journal of Physical Chemistry LettersVol. 16(18)
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)
Openalex Percentile: Top 4%
Protein Structure and Dynamics
5.64
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.