Ryder Sean P, Strobel Scott A
Yale University, Department of Molecular Biophysics and Biochemistry, 260 Whitney Avenue, New Haven, CT 06520-8114, USA.
Nucleic Acids Res. 2002 Mar 15;30(6):1287-91. doi: 10.1093/nar/30.6.1287.
Great strides in understanding the molecular underpinnings of RNA catalysis have been achieved with advances in RNA structure determination by NMR spectroscopy and X-ray crystallography. Despite these successes the functional relevance of a given structure can only be assessed upon comparison with biochemical studies performed on functioning RNA molecules. The hairpin ribozyme presents an excellent case study for such a comparison. The active site is comprised of two stems each with an internal loop that forms a series of non-canonical base pairs. These loops dock into each other to create an active site for catalysis. Recently, three independent structures have been determined for this catalytic RNA, including two NMR structures of the isolated loop A and loop B stems and a high-resolution crystal structure of both loops in a docked conformation. These structures differ significantly both in their tertiary fold and the nature of the non-canonical base pairs formed within each loop. Several of the chemical groups required to achieve a functioning hairpin ribozyme have been determined by nucleotide analog interference mapping (NAIM). Here we compare the three hairpin structures with previously published NAIM data to assess the convergence between the structural and functional data. While there is significant disparity between the interference data and the individual NMR loop structures, there is almost complete congruity with the X-ray structure. The only significant differences cluster around an occluded pocket adjacent to the scissile phosphate. These local differences may suggest a role for these atoms in the transition state, either directly in chemistry or via a local structural rearrangement.
随着核磁共振光谱法和X射线晶体学在RNA结构测定方面取得进展,我们在理解RNA催化的分子基础方面迈出了巨大的步伐。尽管取得了这些成功,但只有在与对功能性RNA分子进行的生化研究进行比较时,才能评估给定结构的功能相关性。发夹状核酶为这种比较提供了一个很好的案例研究。活性位点由两个茎组成,每个茎都有一个内部环,形成一系列非经典碱基对。这些环相互对接,形成一个催化活性位点。最近,已经确定了这种催化RNA的三种独立结构,包括分离的环A和环B茎的两种核磁共振结构,以及处于对接构象的两个环的高分辨率晶体结构。这些结构在其三级折叠以及每个环内形成的非经典碱基对的性质方面都有显著差异。通过核苷酸类似物干扰图谱(NAIM)已经确定了实现功能性发夹状核酶所需的几个化学基团。在这里,我们将三种发夹状结构与先前发表的NAIM数据进行比较,以评估结构数据和功能数据之间的一致性。虽然干扰数据与单个核磁共振环结构之间存在显著差异,但与X射线结构几乎完全一致。唯一显著的差异集中在与切割磷酸相邻的一个封闭口袋周围。这些局部差异可能表明这些原子在过渡态中发挥作用,要么直接参与化学反应,要么通过局部结构重排。