Probing the effect of PEG-DNA interactions and buffer viscosity on tethered DNA in shear flow

DNA flow-stretching is a widely employed, powerful technique for investigating the mechanisms of DNA-binding proteins involved in compacting and organizing chromosomal DNA. We combine single-molecule DNA flow-stretching experiments with Brownian dynamics simulations to study the effect of the crowding agent polyethylene glycol (PEG) in these experiments. PEG interacts with DNA by an excluded volume effect, resulting in compaction of single, free DNA molecules in PEG solutions. In addition, PEG increases the viscosity of the buffer solution. By stretching surface-tethered bacteriophage lambda DNA in a flow cell and tracking the positions of a quantum dot labeled at the free DNA end using total internal reflection fluorescence (TIRF) microscopy, we find that higher PEG concentrations result in increased end-to-end length of flow-stretched DNA and decreased fluctuations of the free DNA end. To better understand our experimental results, we perform Brownian dynamics simulations of a bead-spring chain model of flow-stretched DNA in a viscous buffer that models the excluded volume effect of PEG by an effective attractive interaction between DNA segments. We find quantitative agreement between our model and the experimental results for suitable PEG-DNA interaction parameters.

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Publication Details

Journal
PLoS ONE
Published
2025-08-25
DOI
https://doi.org/10.1371/journal.pone.0329961
Citations
1
Primary Topic
Nanopore and Nanochannel Transport Studies
Type
article
Field-Weighted Citation Impact
0.67

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article

Probing the effect of PEG-DNA interactions and buffer viscosity on tethered DNA in shear flow

Jefferson Reinoza, HyeongJun Kim, Andreas Hanke, Fatema Tuz Zohra et al.
1 citations
PLoS ONE
Nanopore and Nanochannel Transport Studies
0.67
article

Probing the effect of PEG-DNA interactions and buffer viscosity on tethered DNA in shear flow

Jefferson Reinoza, HyeongJun Kim, Andreas Hanke, Fatema Tuz Zohra, Huda Al-Zuhairi
article en
1 citations

Abstract

DNA flow-stretching is a widely employed, powerful technique for investigating the mechanisms of DNA-binding proteins involved in compacting and organizing chromosomal DNA. We combine single-molecule DNA flow-stretching experiments with Brownian dynamics simulations to study the effect of the crowding agent polyethylene glycol (PEG) in these experiments. PEG interacts with DNA by an excluded volume effect, resulting in compaction of single, free DNA molecules in PEG solutions. In addition, PEG increases the viscosity of the buffer solution. By stretching surface-tethered bacteriophage lambda DNA in a flow cell and tracking the positions of a quantum dot labeled at the free DNA end using total internal reflection fluorescence (TIRF) microscopy, we find that higher PEG concentrations result in increased end-to-end length of flow-stretched DNA and decreased fluctuations of the free DNA end. To better understand our experimental results, we perform Brownian dynamics simulations of a bead-spring chain model of flow-stretched DNA in a viscous buffer that models the excluded volume effect of PEG by an effective attractive interaction between DNA segments. We find quantitative agreement between our model and the experimental results for suitable PEG-DNA interaction parameters.

PLoS ONEVol. 20(8)
The University of Texas Rio Grande Valley (US)
National Institutes of Health, National Institute of General Medical Sciences
Openalex Percentile: Top 28%
Nanopore and Nanochannel Transport Studies
0.67
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