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Updated: Jul 19, 2026

Using Solution NMR to Characterize Biomolecular Condensates Under Biphasic Conditions
Published on: April 17, 2026
RNA condensation and the wetting transition.
Toan T Nguyen1, Robijn F Bruinsma
1Department of Physics and Astronomy, University of California-Los Angeles, 475 Portola Plaza, Los Angeles, California 90095, USA.
A new theory explains how large RNA molecules condense on surfaces, similar to fluid wetting. This model predicts distinct density profiles but can break down due to instability, causing RNA to clump.
Area of Science:
- Physical Chemistry
- Biophysics
- Materials Science
Background:
- Condensation of large molecules like RNA on surfaces is crucial for biological processes.
- Understanding the physical mechanisms governing RNA adsorption is essential for controlling its behavior.
Purpose of the Study:
- To develop a continuum theory describing the condensation of large, soluble, single-stranded RNA molecules on attractive substrates.
- To explain the formation of density profiles and identify conditions where the condensation process deviates from standard wetting behavior.
Main Methods:
- Utilized a continuum theory framework.
- Employed the mean-field approximation, drawing parallels to the Cahn-de Gennes description of wetting fluids.
- Analyzed the stability of the adsorbed RNA film.
Main Results:
- The theory successfully explains the development of sharply defined RNA density profiles after a prewetting surface phase transition.
- Identified a capillary instability in the adsorbed RNA film.
- Demonstrated that this instability can cause the film to decompose into segregated, non-overlapping molecules, breaking the analogy with simple wetting fluids.
Conclusions:
- The developed continuum theory provides a robust framework for understanding RNA condensation on surfaces.
- The study highlights the importance of capillary instabilities in the behavior of adsorbed large RNA molecules.
- The findings offer insights into the self-assembly and phase behavior of nucleic acids at interfaces.
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