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GAAA RNA四环对铕(III)的螯合作用。

Sequestering of Eu(III) by a GAAA RNA tetraloop.

作者信息

Mundoma Claudius, Greenbaum Nancy L

机构信息

Department of Chemistry and Biochemistry, Florida State University, Tallahassee, Florida 32306-4390, USA.

出版信息

J Am Chem Soc. 2002 Apr 10;124(14):3525-32. doi: 10.1021/ja012268b.

DOI:10.1021/ja012268b
PMID:11929239
Abstract

The site-specific binding of metal ions maintains an important role in the structure, thermal stability, and function of folded RNA structures. RNA tetraloops of the "GNRA" family (where N = any base and R = any purine), which owe their unusual stability to base stacking and an extensive hydrogen bonding network, have been observed to bind metal ions having different chemical and geometric properties. We have used laser-induced lanthanide luminescence and isothermal titration calorimetry (ITC) to examine the metal-binding properties of an RNA stem loop of the GNRA family. Previous research has shown that a single Eu(III) ion binds the stem loop fragment in a highly dehydrated site with a K(d) of approximately 12 microM. Curve-fitting analysis of the broad luminescence excitation spectrum of Eu(III) upon complexation with the tetraloop fragment indicates the possibility of two microenvironments that do not differ in hydration number. Binding of Eu(III) to the loop was accompanied by positive enthalpic changes, consistent with energetic cost of removal of water molecules and suggesting that the binding is entropically driven. By comparison, binding of Mg(II) or Mn(II) to the RNA loop, or Eu(III) to the DNA analogue of the loop, was associated with exothermic changes, consistent with predominantly outer-sphere coordination. These results suggest specific binding, most probably involving ligands on the 5' side of the loop.

摘要

金属离子的位点特异性结合在折叠RNA结构的结构、热稳定性和功能中起着重要作用。“GNRA”家族(其中N = 任意碱基,R = 任意嘌呤)的RNA四环由于碱基堆积和广泛的氢键网络而具有异常的稳定性,已观察到它们能结合具有不同化学和几何性质的金属离子。我们利用激光诱导镧系元素发光和等温滴定量热法(ITC)来研究GNRA家族RNA茎环的金属结合特性。先前的研究表明,单个Eu(III)离子在高度脱水的位点结合茎环片段,解离常数(K(d))约为12微摩尔。Eu(III)与四环片段络合时其宽发光激发光谱的曲线拟合分析表明,存在两种水化数无差异的微环境。Eu(III)与环的结合伴随着正的焓变,这与去除水分子的能量成本一致,表明这种结合是由熵驱动的。相比之下,Mg(II)或Mn(II)与RNA环的结合,或Eu(III)与环的DNA类似物结合,都伴随着放热变化,这与主要是外层球配位一致。这些结果表明存在特异性结合,最有可能涉及环5'侧的配体。

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