| Literature DB >> 34358322 |
Yuchen Wang1, Jenny V Le1,2, Kyle Crocker3, Michael A Darcy3, Patrick D Halley1, Dengke Zhao3, Nick Andrioff4, Cassie Croy1, Michael G Poirier2,3,5, Ralf Bundschuh2,3,5,6, Carlos E Castro1,2.
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.Entities:
Mesh:
Substances:
Year: 2021 PMID: 34358322 PMCID: PMC8421221 DOI: 10.1093/nar/gkab656
Source DB: PubMed Journal: Nucleic Acids Res ISSN: 0305-1048 Impact factor: 19.160