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Updated: Jul 12, 2026

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Single-Molecule Measurement of Protein Interaction Dynamics Within Biomolecular Condensates
Published on: January 5, 2024
Single-Molecule Dwell Times in Biomolecular Condensates
Fengshuo Yang1, Roumita Moulick1, Cailing Wang1,2
1Department of Biophysics, Johns Hopkins University, Baltimore, Maryland 21218, USA.
Biorxiv : the Preprint Server for Biology
|July 10, 2026
Summary
Biomolecular condensates are dynamic compartments. Our theory reveals how molecule dwell times reveal escape mechanisms, distinguishing diffusion from barrier-limited transport for natural and synthetic systems.
Area of Science:
- Biophysics
- Cell Biology
- Biochemistry
Background:
- Biomolecular condensates are essential membrane-free organelles.
- Molecule dwell time within condensates dictates their function.
- Understanding molecular dynamics is key to condensate biology.
Purpose of the Study:
- To develop a theoretical framework for biomolecular condensate dwell-time distributions.
- To link dwell-time signatures to underlying molecular escape mechanisms.
- To provide insights into the physical principles governing condensate function.
Main Methods:
- Analytical theory development based on single-molecule measurements.
- Modeling of molecular transport within dense phases.
- Analysis of dwell-time distributions to identify escape kinetics.
Main Results:
- Predicted dwell-time distributions show power-law followed by exponential decay.
- A -1.5 power law indicates diffusion-limited escape.
- A -0.5 power law signifies interfacial barrier-crossing-limited escape.
Conclusions:
- Dwell-time distribution shapes directly report on molecular retention mechanisms.
- The theory distinguishes between diffusion and barrier-limited escape pathways.
- Findings have broad implications for understanding and engineering biomolecular condensates.
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