Seebald Leah M, DeMott Christopher M, Ranganathan Srivathsan, Asare-Okai Papa Nii, Glazunova Anastasia, Chen Alan, Shekhtman Alexander, Royzen Maksim
Department of Chemistry, University at Albany, SUNY, 1400 Washington Ave. Albany, NY 12222, United States.
Department of Chemistry, University at Albany, SUNY, 1400 Washington Ave. Albany, NY 12222, United States.
J Inorg Biochem. 2017 May;170:202-208. doi: 10.1016/j.jinorgbio.2017.02.024. Epub 2017 Feb 24.
Paramagnetic resonance enhancement (PRE) is an NMR technique that allows studying three-dimensional structures of RNA-protein complexes in solution. RNA strands are typically spin labeled using nitroxide reagents, which provide minimal perturbation to the native structure. The current work describes an alternative approach, which is based on a Co-based probe that can be covalently attached to RNA in the vicinity of the protein's binding site using 'click' chemistry. Similar to nitroxide spin labels, the transition metal based probe is capable of attenuating NMR signal intensities from protein residues localized <40Å away. The extent of attenuation is related to the probe's distance, thus allowing for construction of the protein's contact surface map. This new paradigm has been applied to study binding of HIV-1 nucleocapsid protein 7, NCp7, to a model RNA pentanucleotide.
顺磁共振增强(PRE)是一种核磁共振技术,可用于研究溶液中RNA-蛋白质复合物的三维结构。RNA链通常使用氮氧化物试剂进行自旋标记,这种试剂对天然结构的干扰最小。目前的工作描述了一种替代方法,该方法基于一种钴基探针,可使用“点击”化学方法将其共价连接到蛋白质结合位点附近的RNA上。与氮氧化物自旋标记类似,基于过渡金属的探针能够减弱距离小于40Å的蛋白质残基的NMR信号强度。衰减程度与探针的距离有关,从而可以构建蛋白质的接触表面图谱。这种新范式已应用于研究HIV-1核衣壳蛋白7(NCp7)与模型RNA五核苷酸的结合。