Zeglis Brian M, Barton Jacqueline K
Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, USA.
J Am Chem Soc. 2006 May 3;128(17):5654-5. doi: 10.1021/ja061409c.
A fluorescent metallointercalator conjugate that selectively targets DNA base mismatches has been synthesized by coupling an organic fluorophore to a bulky Rh intercalator containing the chrysenequinone diimine ligand. Ion pairing between the cationic Rh and anionic fluorophore moieties dramatically quenches the fluorescence of the conjugate in solution and in the presence of matched DNA. However, in the presence of mismatched DNA, the fluorescence of the conjugate is increased >300%. This increase in fluorescence is attributed to the loss in intramolecular quenching associated with DNA binding; intercalation of the Rh moiety into the mismatched site can lead to electrostatic repulsion of the anionic fluorophore away from the DNA phosphate backbone and Rh. Denaturing PAGE experiments with 32P-labeled oligonucleotides indicate that the conjugate selectively binds the mismatched DNA with a binding affinity of 6 x 105 M-1 and, upon irradiation, cleaves the DNA backbone neighboring the mismatched site.
通过将有机荧光团与含有屈醌二亚胺配体的大体积铑嵌入剂偶联,合成了一种选择性靶向DNA碱基错配的荧光金属嵌入剂共轭物。阳离子铑与阴离子荧光团部分之间的离子配对显著淬灭了共轭物在溶液中和存在匹配DNA时的荧光。然而,在存在错配DNA的情况下,共轭物的荧光增加了300%以上。这种荧光增加归因于与DNA结合相关的分子内淬灭的丧失;铑部分嵌入错配位点可导致阴离子荧光团从DNA磷酸主链和铑发生静电排斥。用32P标记的寡核苷酸进行的变性聚丙烯酰胺凝胶电泳实验表明,该共轭物以6×105 M-1的结合亲和力选择性结合错配DNA,并在照射后切割错配位点附近的DNA主链。