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Structure of the cytosine-cytosine mismatch in the thymidylate synthase mRNA binding site and analysis of its interaction with the aminoglycoside paromomycin.

机译:胸苷酸合酶mRNA结合位点中胞嘧啶-胞嘧啶错配的结构及其与氨基糖苷巴龙霉素相互作用的分析。

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摘要

The structure of a cytosine-cytosine (CC) mismatch-containing RNA molecule derived from a hairpin structure in the thymidylate synthase mRNA that binds the aminoglycoside paromomycin with high affinity was determined using nuclear magnetic resonance (NMR) spectroscopy. The cytosines in the mismatch form a noncanonical base pair where both cytosines are uncharged and stack within the stem of the RNA structure. Binding to paromomycin was analyzed using isothermal titration calorimetry (ITC) to demonstrate the necessity of the CC mismatch and to determine the affinity dissociation constant of this RNA to paromomycin to be 0.5 +/- 0.3 microM. The CC mismatch, and the neighboring GC base pairs experienced the highest degree of chemical shift changes in their H6 and H5 resonances indicating that paromomycin binds in the major groove at the CC mismatch site. In comparing the structure of CC mismatch RNA with a fully Watson-Crick GC base paired stem, the CC mismatch is shown to confer a widening of the major groove. This widening, combined with the dynamic nature of the CC mismatch, enables binding of paromomycin to this RNA molecule.
机译:使用核磁共振(NMR)光谱法确定了源自胸苷酸合酶mRNA中发夹结构的高亲和力结合氨基糖苷巴龙霉素的含胞嘧啶-胞嘧啶(CC)错配的RNA分子的结构。错配的胞嘧啶形成非规范碱基对,其中两个胞嘧啶均不带电荷并堆叠在RNA结构的茎中。使用等温滴定量热法(ITC)分析与巴龙霉素的结合,以证明CC错配的必要性,并将该RNA与巴龙霉素的亲和解离常数确定为0.5 +/- 0.3 microM。 CC错配,以及邻近的GC碱基对在其H6和H5共振中经历了最高程度的化学位移变化,表明巴龙霉素结合在CC错配位点的主要沟中。通过比较CC错配RNA与完全沃森-克里克(Watson-Crick)GC碱基配对茎的结构,显示出CC错配可扩大主沟。这种扩大,再加上CC错配的动态性质,使得巴龙霉素可以与该RNA分子结合。

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