Teeling-Smith Richelle M, Jung Young Woo, Scozzaro Nicolas, Cardellino Jeremy, Rampersaud Isaac, North Justin A, Šimon Marek, Bhallamudi Vidya P, Rampersaud Arfaan, Johnston-Halperin Ezekiel, Poirier Michael G, Hammel P Chris
Department of Physics, The Ohio State University, Columbus, Ohio.
Samsung Electronics, San #24 Nongseo-Dong, Giheung-Gu, Yongin-City, Gyonggi-Do, Korea.
Biophys J. 2016 May 10;110(9):2044-52. doi: 10.1016/j.bpj.2016.03.022.
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.
电子顺磁共振(EPR)是一种成熟且强大的用于研究原子尺度生物分子结构和动力学的方法,通常需要超过10¹²个标记的生物分子。单分子测量能更好地洞察在整体测量中可能被掩盖的异质性行为,对于阐明生物分子功能背后的分子机制往往至关重要。在此,我们报告了对单个标记生物分子的EPR测量。我们用一个含有氮空位中心的单个纳米金刚石选择性地标记单个双链DNA分子,并通过光学检测纳米金刚石探针中氮空位自旋的顺磁共振。光谱分析表明,纳米金刚石探针具有完全的旋转自由度,并且与横向自旋弛豫时间相比,纳米金刚石探针重新定向的特征时间尺度较慢。这种对单个纳米金刚石标记DNA的EPR光谱学演示为复杂生物分子系统的单分子磁共振研究发展奠定了基础。