Legault P, Hoogstraten C G, Metlitzky E, Pardi A
Department of Chemistry and Biochemistry, University of Colorado at Boulder, Campus Box 215, Boulder, CO, 80309-0215, USA.
J Mol Biol. 1998 Nov 27;284(2):325-35. doi: 10.1006/jmbi.1998.2181.
The in vitro selected lead-dependent ribozyme is among the smallest and simplest of the known catalytic RNA motifs and has a unique metal ion specificity for divalent lead. The conformation and dynamics of this ribozyme are analyzed here by NMR and chemical probing experiments. Complete assignments of the 1H, 13C, and 15N resonances have been made, and the NMR chemical shift changes in the presence of Pb2+, Mg2+ or high concentrations of Na+ show that there is no significant structural change upon addition of either activating (Pb2+) or inhibitory (Mg2+) divalent ions. The 13C NMR relaxation data indicate substantial dynamic fluctuations on various time-scales for active-site residues in this ribozyme. The combination of chemical probing and NMR experiments reveals a picture of the active site for the lead-dependent ribozyme that has both ordered and dynamic features.
体外筛选得到的铅依赖型核酶是已知催化RNA基序中最小且最简单的之一,并且对二价铅具有独特的金属离子特异性。本文通过核磁共振(NMR)和化学探针实验分析了这种核酶的构象和动力学。已完成对1H、13C和15N共振的完全归属,并且在存在Pb2+、Mg2+或高浓度Na+时的NMR化学位移变化表明,添加激活(Pb2+)或抑制(Mg2+)二价离子后没有显著的结构变化。13C NMR弛豫数据表明,该核酶活性位点残基在各种时间尺度上存在大量动态波动。化学探针和NMR实验的结合揭示了铅依赖型核酶活性位点兼具有序和动态特征的图景。