| Literature DB >> 27166812 |
Richelle M Teeling-Smith1, Young Woo Jung2, Nicolas Scozzaro1, Jeremy Cardellino1, Isaac Rampersaud3, Justin A North1, Marek Šimon1, Vidya P Bhallamudi1, Arfaan Rampersaud3, Ezekiel Johnston-Halperin1, Michael G Poirier1, P Chris Hammel4.
Abstract
Electron paramagnetic resonance (EPR), an established and powerful methodology for studying atomic-scale biomolecular structure and dynamics, typically requires in excess of 10(12) labeled biomolecules. Single-molecule measurements provide improved insights into heterogeneous behaviors that can be masked in ensemble measurements and are often essential for illuminating the molecular mechanisms behind the function of a biomolecule. Here, we report EPR measurements of a single labeled biomolecule. We selectively label an individual double-stranded DNA molecule with a single nanodiamond containing nitrogen-vacancy centers, and optically detect the paramagnetic resonance of nitrogen-vacancy spins in the nanodiamond probe. Analysis of the spectrum reveals that the nanodiamond probe has complete rotational freedom and that the characteristic timescale for reorientation of the nanodiamond probe is slow compared with the transverse spin relaxation time. This demonstration of EPR spectroscopy of a single nanodiamond-labeled DNA provides the foundation for the development of single-molecule magnetic resonance studies of complex biomolecular systems.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27166812 PMCID: PMC4940449 DOI: 10.1016/j.bpj.2016.03.022
Source DB: PubMed Journal: Biophys J ISSN: 0006-3495 Impact factor: 4.033