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Updated: Jul 23, 2025

A Simple, Robust, and High Throughput Single Molecule Flow Stretching Assay Implementation for Studying Transport of Molecules Along DNA
Published on: October 1, 2017
Role of DNA-DNA sliding friction and nonequilibrium dynamics in viral genome ejection and packaging
Mounir Fizari1, Nicholas Keller1, Paul J Jardine2
1Department of Physics, University of California, San Diego, La Jolla, CA 92093, USA.
Abstract:
Many viruses eject their DNA via a nanochannel in the viral shell, driven by internal forces arising from the high-density genome packing. The speed of DNA exit is controlled by friction forces that limit the molecular mobility, but the nature of this friction is unknown. We introduce a method to probe the mobility of the tightly confined DNA by measuring DNA exit from phage phi29 capsids with optical tweezers. We measure extremely low initial exit velocity, a regime of exponentially increasing velocity, stochastic pausing that dominates the kinetics and large dynamic heterogeneity. Measurements with variable applied force provide evidence that the initial velocity is controlled by DNA-DNA sliding friction, consistent with a Frenkel-Kontorova model for nanoscale friction. We confirm several aspects of the ejection dynamics predicted by theoretical models. Features of the pausing suggest that it is connected to the phenomenon of 'clogging' in soft matter systems. Our results provide evidence that DNA-DNA friction and clogging control the DNA exit dynamics, but that this friction does not significantly affect DNA packaging.
Insights
Viral DNA ejection is governed by DNA-DNA friction and clogging, not packaging friction. Optical tweezers reveal low initial velocity and dynamic pausing during DNA exit from phage phi29 capsids.
Area of Science:
- Biophysics
- Molecular Virology
- Nanotechnology
Background:
- Viruses eject DNA through nanochannels, driven by internal genome pressure.
- The precise nature of friction limiting DNA exit velocity remains poorly understood.
Purpose of the Study:
- To investigate the friction forces controlling DNA exit dynamics from viral capsids.
- To probe the molecular mobility of confined DNA using advanced biophysical techniques.
Main Methods:
- Utilized optical tweezers to measure the DNA exit velocity from phage phi29 capsids.
- Applied variable forces to analyze the relationship between force and DNA mobility.
- Observed and characterized stochastic pausing and dynamic heterogeneity during ejection.
Main Results:
- Measured extremely low initial DNA exit velocities.
- Identified DNA-DNA sliding friction as the primary determinant of initial velocity, aligning with nanoscale friction models.
- Observed significant stochastic pausing and dynamic heterogeneity, suggesting a 'clogging' phenomenon.
Conclusions:
- DNA-DNA friction and clogging critically control viral DNA exit dynamics.
- This friction does not appear to significantly impede the DNA packaging process.
- The findings provide insights into nanoscale friction and molecular transport in biological systems.
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