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Luminescence of Ru(bpy)2(dppz)2+ Bound to RNA Mismatches

机译:Ru(bpy)2(dppz) 2+的发光与RNA不匹配

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摘要

The luminescence of rac-[Ru(bpy)2(dppz)]2+ (bpy = 2,2′-bipyridine and dppz = dipyrido[3,2-a:2′,3′-c]phenazine) was explored in the presence of RNA oligonucleotides containing a single RNA mismatch (CA and GG) in order to develop a probe for RNA mismatches. While there is minimal luminescence of [Ru(bpy)2(dppz)]2+ in the presence of matched RNA due to weak binding, the luminescence is significantly enhanced in the presence of a single CA mismatch. The luminescence differential between CA mismatched and matched RNA is substantially higher compared to the DNA analogue, and therefore, [Ru(bpy)2(dppz)]2+ appears to be also a sensitive light switch probe for a CA mismatch in duplex RNA. Although the luminescence intensity is lower in the presence of RNA than DNA, Förster resonance energy transfer (FRET) between the donor ruthenium complex and FRET acceptor SYTO 61 is successfully exploited to amplify the luminescence in the presence of the mismatch. Luminescence and quenching studies with sodium iodide suggest that [Ru(bpy)2(dppz)]2+ binds to these mismatches via metalloinsertion from the minor groove. This work provides further evidence that metalloinsertion is a general binding mode of octahedral metal complexes to thermodynamically destabilized mismatches not only in DNA, but also in RNA.
机译:rac- [Ru(bpy)2(dppz)] 2 + (bpy = 2,2'-联吡啶,dppz = dipyrido [3,2-a:2',3'- c]非那嗪在含有单个RNA错配(CA和GG)的RNA寡核苷酸存在下进行了研究,以便开发出RNA错配的探针。尽管由于弱结合而在匹配的RNA存在下[Ru(bpy)2(dppz)] 2 + 的发光最小,但是在单个CA不匹配的情况下,发光显着增强。与DNA类似物相比,CA错配和匹配的RNA之间的发光差异要高得多,因此[Ru(bpy)2(dppz)] 2 + 似乎也是一种灵敏的光开关探针双链RNA中的CA不匹配。尽管存在RNA时的发光强度低于DNA,但供体钌配合物与FRET受体SYTO 61之间的Förster共振能量转移(FRET)已成功地用于放大错配存在下的发光。碘化钠的发光和猝灭研究表明,[Ru(bpy)2(dppz)] 2 + 通过小沟的金属插入与这些错配结合。这项工作提供了进一步的证据,证明金属插入是八面体金属络合物与热力学上不稳定的错配的一般结合方式,不仅在DNA中,而且在RNA中。

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