Spontaneous enrichment of client molecules at phase boundaries of biomolecular condensates

The interface of biomolecular condensates plays a critical role in regulating many biochemical processes, such as protein aggregation and enzymatic activity. Targeted modulation of these interfaces offers a promising route for engineering condensates and correcting aberrant behaviors. However, the physical principles underlying the preferential localization of molecules at condensate interfaces are poorly understood. In this study, we develop an analytical theory for the enrichment of client molecules at the interface of phase-separated systems. We derive minimal conditions for interfacial localization based on pairwise interaction parameters. Our results reveal a general mechanism for passive interface-driven enrichment, which could guide the design of macromolecules that localize at the interface of biomolecular condensates.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2026-02-18
DOI
https://doi.org/10.1063/5.0300773
Primary Topic
Surface Chemistry and Catalysis
Type
article
Field-Weighted Citation Impact
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article

Spontaneous enrichment of client molecules at phase boundaries of biomolecular condensates

Alexander J. Dear, Thomas C. T. Michaels, Marco Curschellas, Vitus I. Getzinger
The Journal of Chemical Physics
Surface Chemistry and Catalysis
article

Spontaneous enrichment of client molecules at phase boundaries of biomolecular condensates

Alexander J. Dear, Thomas C. T. Michaels, Marco Curschellas, Vitus I. Getzinger
article en

Abstract

The interface of biomolecular condensates plays a critical role in regulating many biochemical processes, such as protein aggregation and enzymatic activity. Targeted modulation of these interfaces offers a promising route for engineering condensates and correcting aberrant behaviors. However, the physical principles underlying the preferential localization of molecules at condensate interfaces are poorly understood. In this study, we develop an analytical theory for the enrichment of client molecules at the interface of phase-separated systems. We derive minimal conditions for interfacial localization based on pairwise interaction parameters. Our results reveal a general mechanism for passive interface-driven enrichment, which could guide the design of macromolecules that localize at the interface of biomolecular condensates.

The Journal of Chemical PhysicsVol. 164(7)
ETH Zurich (CH), Life Science Zurich (CH)
Openalex Percentile: Top 51%
Surface Chemistry and Catalysis
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