Atomic force microscopy (AFM) has proven to be a powerful tool for the study of DNA-protein interactions due to its ability to image single molecules at the nanoscale. However, the use of AFM in force spectroscopy to study DNA-protein interactions has been limited. Here we developed a high throughput, AFM based, pulling assay to measure the strength and kinetics of protein bridging of DNA molecules. As a model system, we investigated the interactions between DNA and the Histone-like Nucleoid-Structuring protein (H-NS). We confirmed that H-NS both changes DNA rigidity and forms bridges between DNA molecules. This straightforward methodology provides a high-throughput approach with single-molecule resolution which is widely applicable to study cross-substrate interactions such as DNA-bridging proteins.
CITATION STYLE
Liang, Y., Van Der Valk, R. A., Dame, R. T., Roos, W. H., & Wuite, G. J. L. (2017). Probing the mechanical stability of bridged DNA-H-NS protein complexes by single-molecule AFM pulling. Scientific Reports, 7(1). https://doi.org/10.1038/s41598-017-15477-4
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