Department of Biochemistry, Stanford University, Stanford, California 94305, USA.
Biochemistry. 2010 Mar 30;49(12):2753-62. doi: 10.1021/bi902200n.
Protein enzymes appear to use extensive packing and hydrogen bonding interactions to precisely position catalytic groups within active sites. Because of their inherent backbone flexibility and limited side chain repertoire, RNA enzymes face additional challenges relative to proteins in precisely positioning substrates and catalytic groups. Here, we use the group I ribozyme to probe the existence, establishment, and functional consequences of an extended network of interactions in an RNA active site. The group I ribozyme catalyzes a site-specific attack of guanosine on an oligonucleotide substrate. We previously determined that the hydrogen bond between the exocyclic amino group of guanosine and the 2'-hydroxyl group at position A261 of the Tetrahymena group I ribozyme contributes to overall catalysis. We now use functional data, aided by double mutant cycles, to probe this hydrogen bond in the individual reaction steps of the catalytic cycle. Our results indicate that this hydrogen bond is not formed upon guanosine binding to the ribozyme but instead forms at a later stage of the catalytic cycle. Formation of this hydrogen bond is correlated with other structural rearrangements in the ribozyme's active site that are promoted by docking of the oligonucleotide substrate into the ribozyme's active site, and disruption of this interaction has deleterious consequences for the chemical transformation within the ternary complex. These results, combined with earlier results, provide insight into the nature of the multiple conformational steps used by the Tetrahymena group I ribozyme to achieve its active structure and reveal an intricate, extended network of interactions that is used to establish catalytic interactions within this RNA's active site.
蛋白质酶似乎利用广泛的包装和氢键相互作用,将催化基团精确地定位在活性部位内。由于其固有骨架的灵活性和有限的侧链库,RNA 酶在精确定位底物和催化基团方面面临着比蛋白质更多的挑战。在这里,我们使用 I 组核酶来探测 RNA 活性部位中扩展的相互作用网络的存在、建立和功能后果。I 组核酶催化鸟苷对寡核苷酸底物的特异性攻击。我们之前确定,鸟苷的环外氨基与 Tetrahymena I 组核酶的 A261 位 2'-羟基之间的氢键有助于整体催化。我们现在使用功能数据,并借助双突变循环,在催化循环的各个反应步骤中探测这个氢键。我们的结果表明,这个氢键不是在鸟苷与核酶结合时形成的,而是在催化循环的后期形成的。这个氢键的形成与核酶活性部位中的其他结构重排相关联,这些重排是由寡核苷酸底物与核酶的活性部位对接所促进的,并且破坏这个相互作用对三元复合物中的化学转化有不良影响。这些结果与早期的结果相结合,提供了对 Tetrahymena I 组核酶用于实现其活性结构的多种构象步骤的本质的深入了解,并揭示了在这个 RNA 的活性部位中建立催化相互作用所使用的复杂的、扩展的相互作用网络。