A nanoscale DNA force spectrometer capable of applying tension and compression on biomolecules
Year: 2021
Type: article
Abstract: Single molecule force spectroscopy is a powerful approach to probe the structure, conformational changes, and kinetic properties of biological and synthetic macromolecules. However, common approaches to apply forces to biomolecules require expensive and cumbersome equipment and relatively large probes such as beads or cantilevers, which limits their use for many environments and makes integrating with other methods challenging. Furthermore, existing methods have key limitations such as an inability to apply compressive forces on single molecules. We report a nanoscale DNA force spectrometer (nDFS), which is based on a DNA origami hinge with tunable mechanical and dynamic properties. The angular free energy landscape of the nDFS can be engineered across a wide range through substitution of less than 5% of the strand components. We further incorporate a removable strut that enables reversible toggling of the nDFS between open and closed states to allow for actuated application of tensile and compressive forces. We demonstrate the ability to apply compressive forces by inducing a large bend in a 249bp DNA molecule, and tensile forces by inducing DNA unwrapping of a nucleosome sample. These results establish a versatile tool for force spectroscopy and robust methods for designing nanoscale mechanical devices with tunable force application.
Source: Nucleic Acids Research
DOI: 10.1093/nar/gkab656
Institution: The Ohio State University
Language: English
Subfield: Atomic and Molecular Physics, and Optics
Field: Physics and Astronomy
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $3,800
Awards: Regulatory Mechanisms of Linker Histones and Their Post-Translational Modifications, EFRI CEE: DNA origami tools to engineer chromatin structure and function in live cells, G36614667, Quantitative modeling of nucleic acid-protein interactions, Understanding how two related mammalian histone acetyl transferase co-activators, SAGA and ATAC, differentially regulate chromatin dynamics and transcription, Mechanistic studies of heterochromatin mesoscale structural dynamics with DNA origami nanotechnology, Cancer Center Support Grant
OpenAlex ID: W3189249173
