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Updated: Jun 22, 2026

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Published on: February 7, 2019
Quantifying hopping and jumping in facilitated diffusion of DNA-binding proteins
C Loverdo1, O Bénichou, R Voituriez
1Laboratoire de Physique Théorique de la Matière Condensée (UMR 7600), Université Pierre et Marie Curie, 4 Place Jussieu, 75255 Paris Cedex France.
DNA-binding proteins locate targets faster using 3D excursions and linear diffusion. This study quantifies these movements, supporting experiments with EcoRV and extending analysis to crowded cellular environments.
Area of Science:
- Biophysics
- Molecular Biology
- Biochemistry
Background:
- Facilitated diffusion enhances DNA-binding protein target location.
- This process involves a combination of three-dimensional (3D) excursions and linear diffusion along DNA.
Purpose of the Study:
- To explicitly calculate the distribution of relocation lengths for 3D excursions of DNA-binding proteins.
- To quantify short-range correlated excursions (hops) and long-range uncorrelated jumps.
- To extend the analysis to anomalous 3D diffusion in crowded cellular media.
Main Methods:
- Theoretical calculation of relocation length distributions.
- Analysis of short-range (hops) and long-range (jumps) diffusion components.
- Modeling of anomalous 3D diffusion.
Main Results:
- The study provides explicit calculations for the distribution of 3D excursion relocation lengths.
- Quantification of both short-range hops and long-range jumps in protein diffusion.
- Results align with single-molecule experiments on EcoRV enzyme diffusion on DNA.
Conclusions:
- The findings support the model of facilitated diffusion involving 3D excursions and linear diffusion.
- The quantification of different diffusion types offers insights into protein-DNA interactions.
- The extension to anomalous diffusion addresses biologically relevant crowded cellular conditions.
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