Guiding Peptide Kinetics via Collective-Variable Tuning of Free-Energy Barriers

Fuente: arXiv
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Main Authors: Zhilkin, Alexander, Medaparambath, Muralika, Mendels, Dan
Format: Preprint
Published: 2026
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author Zhilkin, Alexander
Medaparambath, Muralika
Mendels, Dan
author_facet Zhilkin, Alexander
Medaparambath, Muralika
Mendels, Dan
contents While recent advances in AI have transformed protein structure prediction, protein function is also strongly influenced by the thermodynamic and kinetic features encoded in its underlying free-energy surface. Here, we propose a data-efficient framework for engineering protein conformational kinetics by rationally reshaping free-energy landscapes to control transition rates. Built on the Collective Variables for Free Energy Surface Tailoring (CV-FEST) framework, the approach is validated on point mutations of the miniprotein Chignolin. The framework relies on Harmonic Linear Discriminant Analysis (HLDA)-based collective variables (CVs) constructed from short molecular dynamics trajectories confined to metastable folded and unfolded basins, requiring only limited local sampling rather than exhaustive rare-event simulations. Notably, the HLDA CV derived solely from the wild-type system provides residue-level scores that predict whether mutations at specific positions are likely to accelerate or slow unfolding transitions. Furthermore, the leading HLDA eigenvalue associated with the derived CV, a quantitative measure of the one-dimensional statistical separation between folded and unfolded ensembles, is significantly correlated with transition rates across mutations. Together, these results suggest that mutation-dependent kinetic effects can be inferred from minimal in-basin sampling, providing a practical route for guiding peptide and protein engineering through collective-variable design, free-energy surface engineering, and data-efficient molecular simulation.
format Preprint
id arxiv_https___arxiv_org_abs_2602_19936
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Guiding Peptide Kinetics via Collective-Variable Tuning of Free-Energy Barriers
Zhilkin, Alexander
Medaparambath, Muralika
Mendels, Dan
Biological Physics
While recent advances in AI have transformed protein structure prediction, protein function is also strongly influenced by the thermodynamic and kinetic features encoded in its underlying free-energy surface. Here, we propose a data-efficient framework for engineering protein conformational kinetics by rationally reshaping free-energy landscapes to control transition rates. Built on the Collective Variables for Free Energy Surface Tailoring (CV-FEST) framework, the approach is validated on point mutations of the miniprotein Chignolin. The framework relies on Harmonic Linear Discriminant Analysis (HLDA)-based collective variables (CVs) constructed from short molecular dynamics trajectories confined to metastable folded and unfolded basins, requiring only limited local sampling rather than exhaustive rare-event simulations. Notably, the HLDA CV derived solely from the wild-type system provides residue-level scores that predict whether mutations at specific positions are likely to accelerate or slow unfolding transitions. Furthermore, the leading HLDA eigenvalue associated with the derived CV, a quantitative measure of the one-dimensional statistical separation between folded and unfolded ensembles, is significantly correlated with transition rates across mutations. Together, these results suggest that mutation-dependent kinetic effects can be inferred from minimal in-basin sampling, providing a practical route for guiding peptide and protein engineering through collective-variable design, free-energy surface engineering, and data-efficient molecular simulation.
title Guiding Peptide Kinetics via Collective-Variable Tuning of Free-Energy Barriers
topic Biological Physics
url https://arxiv.org/abs/2602.19936