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Updated: Jun 9, 2025

Studying DNA Looping by Single-Molecule FRET
Published on: June 28, 2014
DNA supercoiling enhances DNA condensation by ParB proteins
Alejandro Martin-Gonzalez1, Miloš Tišma1, Brian T Analikwu1
1Department of Bionanoscience, Kavli Institute of Nanoscience Delft, Delft University of Technology, Van der Massweg 9, 2629HZ Delft, Netherlands.
Abstract:
The ParABS system plays a critical role in bacterial chromosome segregation. The key component of this system, ParB, loads and spreads along DNA to form a local protein-DNA condensate known as a partition complex. As bacterial chromosomes are heavily supercoiled due to the continuous action of RNA polymerases, topoisomerases and nucleoid-associated proteins, it is important to study the impact of DNA supercoiling on the ParB-DNA partition complex formation. Here, we use an in-vitro single-molecule assay to visualize ParB on supercoiled DNA. Unlike most DNA-binding proteins, individual ParB proteins are found to not pin plectonemes on supercoiled DNA, but freely diffuse along supercoiled DNA. We find that DNA supercoiling enhances ParB-DNA condensation, which initiates at lower ParB concentrations than on DNA that is torsionally relaxed. ParB proteins induce a DNA-protein condensate that strikingly absorbs all supercoiling writhe. Our findings provide mechanistic insights that have important implications for our understanding of bacterial chromosome organization and segregation.
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