Kinetic Superselectivity in Multivalent Binding

Multivalent binding employs multiple simultaneous supramolecular interactions, increasing avidity and selectivity compared with monovalent binding. While equilibrium aspects of multivalency are well characterized, nonequilibrium behavior remains poorly understood. By combining experiments on hyaluronic acid polymers with kinetic modeling based on stochastic chemical kinetics and molecular dynamics simulations, we systematically investigate the kinetics of multivalent binding. Notably, we find that both association and dissociation kinetics can be more selective than equilibrium binding. We explain this behavior using a two-step binding model featuring a combination of fast, weak and slow, strong interactions. These findings demonstrate a new approach: superselective targeting based on the association rate instead of the equilibrium state. The kinetic theory and experiments presented here provide a fundamental understanding of multivalent kinetics and establish design rules for superselective targeting in out-of-equilibrium systems.

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Publication Details

Journal
The Journal of Physical Chemistry Letters
Published
2026-05-19
DOI
https://doi.org/10.1021/acs.jpclett.6c01096
Primary Topic
Proteoglycans and glycosaminoglycans research
Type
article
Field-Weighted Citation Impact
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article

Kinetic Superselectivity in Multivalent Binding

Galina V. Dubacheva, Tine Curk, Vid Ravnik, Baptiste Chabaud et al.
The Journal of Physical Chemistry Letters
Proteoglycans and glycosaminoglycans research
article

Kinetic Superselectivity in Multivalent Binding

Galina V. Dubacheva, Tine Curk, Vid Ravnik, Baptiste Chabaud, Urban Bren
article en

Abstract

Multivalent binding employs multiple simultaneous supramolecular interactions, increasing avidity and selectivity compared with monovalent binding. While equilibrium aspects of multivalency are well characterized, nonequilibrium behavior remains poorly understood. By combining experiments on hyaluronic acid polymers with kinetic modeling based on stochastic chemical kinetics and molecular dynamics simulations, we systematically investigate the kinetics of multivalent binding. Notably, we find that both association and dissociation kinetics can be more selective than equilibrium binding. We explain this behavior using a two-step binding model featuring a combination of fast, weak and slow, strong interactions. These findings demonstrate a new approach: superselective targeting based on the association rate instead of the equilibrium state. The kinetic theory and experiments presented here provide a fundamental understanding of multivalent kinetics and establish design rules for superselective targeting in out-of-equilibrium systems.

The Journal of Physical Chemistry Letters
University of Primorska (SI), Centre National de la Recherche Scientifique (FR), Johns Hopkins University (US), University of Maribor (SI), Département de Chimie Moléculaire (FR), Institute for Environmental Protection and Sensors (SI), Université Grenoble Alpes (FR)
Openalex Percentile: Top 6%
Proteoglycans and glycosaminoglycans research
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