Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States.
Inorg Chem. 2013 Sep 3;52(17):10131-6. doi: 10.1021/ic401531r. Epub 2013 Aug 22.
The luminescence of rac-Ru(bpy)2(dppz) (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) 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) 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) 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.
研究了含有单个 RNA 错配(CA 和 GG)的寡核苷酸存在时 rac-Ru(bpy)2(dppz)(bpy = 2,2'-联吡啶,dppz = 二吡啶并[3,2-a:2',3'-c]吩嗪)的发光情况,以开发用于 RNA 错配的探针。由于弱结合,在存在匹配 RNA 的情况下,Ru(bpy)2(dppz) 的发光非常微弱,但在存在单个 CA 错配的情况下,发光显著增强。CA 错配和匹配 RNA 之间的发光差异明显高于 DNA 类似物,因此,Ru(bpy)2(dppz) 似乎也是双链 RNA 中 CA 错配的灵敏光开关探针。尽管在存在 RNA 时发光强度比 DNA 低,但可以成功利用供体钌配合物和 FRET 受体 SYTO 61 之间的Förster 共振能量转移(FRET)来放大错配存在时的发光。用碘化钠进行的发光和猝灭研究表明,Ru(bpy)2(dppz) 通过从小沟插入金属来结合这些错配。这项工作进一步证明,金属插入是八面体金属配合物与热力学不稳定错配结合的一般结合模式,不仅在 DNA 中,而且在 RNA 中也是如此。