Trantírek Lukás, Stefl Richard, Masse James E, Feigon Juli, Sklenár Vladimír
National Centre for Biomolecular Research, Faculty of Science, Masaryk University, Koltlárská Brno, Czech Republic.
J Biomol NMR. 2002 May;23(1):1-12. doi: 10.1023/a:1015389118506.
A two-dimensional, quantitative J-correlation NMR experiment for precise measurements of the proton-carbon vicinal coupling constants 3J(C2)/4-H1' and 3J(C6)/8-H1' in uniformly 13C-labeled nucleic acids is presented. To reduce loss of signal due to 1H-13C dipole-dipole relaxation, a multiple-quantum constant time experiment with appropriately incorporated band selective 1H and 13C pulses was applied. The experiment is used to obtain the 3J(C2)/4-H1' and 3J(C6)/8-H1' coupling constants in a uniformly 13C, 15N-labeled [d(G4T4G4)]2 quadruplex. The measured values and glycosidic torsion angles in the G-quadruplex, obtained by restrained molecular dynamics with explicit solvent using the previously published restraints, along with selected data from the literature are used to check and modify existing parameters of the Karplus equations. The parameterizations obtained using glycosidic torsion angles derived from the original solution and recently determined X-ray structures are also compared.
本文介绍了一种二维定量J-相关核磁共振实验,用于精确测量均匀13C标记核酸中质子-碳邻位耦合常数3J(C2)/4-H1'和3J(C6)/8-H1'。为减少由于1H-13C偶极-偶极弛豫导致的信号损失,采用了带有适当合并的带选择性1H和13C脉冲的多量子恒时实验。该实验用于在均匀13C、15N标记的[d(G4T4G4)]2四链体中获得3J(C2)/4-H1'和3J(C6)/8-H1'耦合常数。通过使用先前发表的限制条件在显式溶剂中进行受限分子动力学获得的G-四链体中的测量值和糖苷扭转角,以及文献中的选定数据,用于检查和修改Karplus方程的现有参数。还比较了使用从原始溶液和最近确定的X射线结构得出的糖苷扭转角获得的参数化结果。