Zimmermann G R, Jenison R D, Wick C L, Simorre J P, Pardi A
Department of Chemistry and Biochemistry, University of Colorado, Boulder 80309-0215, USA.
Nat Struct Biol. 1997 Aug;4(8):644-9. doi: 10.1038/nsb0897-644.
To visualize the interplay of RNA structural interactions in a ligand binding site, we have determined the solution structure of a high affinity RNA-theophylline complex using NMR spectroscopy. The structure provides insight into the ability of this in vitro selected RNA to discriminate theophylline from the structurally similar molecule caffeine. Numerous RNA structural motifs combine to form a well-ordered binding pocket where an intricate network of hydrogen bonds and stacking interactions lock the theophylline into the complex. Two internal loops interact to form the binding site which consists of a sandwich of three base triples. The complex also contains novel base-zipper and 1-3-2 stacking motifs, in addition to an adenosine platform and a reversed sugar. An important feature of the RNA is that many of the conserved core residues participate in multiple overlapping tertiary interactions. This complex illustrates how interlocking structural motifs can be assembled into a highly specific ligand-binding site that possesses high levels of affinity and molecular discrimination.
为了可视化配体结合位点中RNA结构相互作用的相互影响,我们利用核磁共振光谱法确定了高亲和力RNA-茶碱复合物的溶液结构。该结构有助于深入了解这种体外筛选的RNA区分茶碱与结构相似分子咖啡因的能力。众多RNA结构基序结合形成一个有序的结合口袋,其中复杂的氢键和堆积相互作用网络将茶碱锁定在复合物中。两个内环相互作用形成由三个碱基三联体组成的三明治结构的结合位点。该复合物除了含有一个腺苷平台和一个反向糖外,还包含新型碱基拉链和1-3-2堆积基序。该RNA的一个重要特征是许多保守的核心残基参与多个重叠的三级相互作用。这种复合物说明了相互连锁的结构基序如何组装成一个具有高亲和力和分子识别能力的高度特异性配体结合位点。