Cobalt(III)porphyrin to target G-quadruplex DNA

被引:30
|
作者
Sabater, Laurent [1 ,2 ]
Fang, Pei-Ju [3 ]
Chang, Chi-Fon [4 ]
De Rache, Aurore [5 ,6 ]
Prado, Enora [7 ]
Dejeu, Jerome [7 ]
Garofalo, Antonio [1 ,2 ]
Lin, Jung-Hsin [3 ,8 ]
Mergny, Jean-Louis [5 ,6 ]
Defrancq, Eric [7 ]
Pratviel, Genevieve [1 ,2 ]
机构
[1] CNRS, Chim Coordinat Lab, F-31077 Toulouse, France
[2] Univ Toulouse, UPS, INPT, Toulouse, France
[3] Acad Sinica, Inst Biomed Sci, Taipei 115, Taiwan
[4] Acad Sinica, Genom Res Ctr, Taipei 115, Taiwan
[5] Univ Bordeaux, ARNA Lab, F-33000 Bordeaux, France
[6] INSERM, IECB, U869, F-33600 Pessac, France
[7] Univ Grenoble Alpes, Dept Chim Mol, UMR CNRS 5250, F-38041 Grenoble 9, France
[8] Acad Sinica, Res Ctr Appl Sci, Taipei 115, Taiwan
关键词
TELOMERIC G-QUADRUPLEX; METAL-COMPLEXES; CATIONIC PORPHYRINS; STRUCTURAL BASIS; END-STACKING; K+ SOLUTION; LIGANDS; BINDING; DUPLEX; RECOGNITION;
D O I
10.1039/c4dt03631j
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
G-quadruplex DNA ligands attract much attention because of their potential use in biology. Indeed they may interfere with G-quadrulex nucleic acid function in cells. Most of the G-quadruplex ligands so far reported (including also metal complexes) are large planar aromatic compounds that interact by pi-pi stacking with an external G-quartet of quadruplex. Porphyrins are well-known G-quadruplex ligands. We report herein a new porphyrin scaffold (meso-tetrakis(4-(N-methyl-pyridinium-2-yl) phenyl) porphyrin) able to strongly and selectively bind to G-quadruplex DNA. We show that even when this porphyrin is metallated with cobalt(III), i.e. it carries two water molecules as axial ligands on the cobalt ion, on each face of the porphyrin, the interaction occurs by a pi-stacking-like mode with an external G-quartet of quadruplex DNA.
引用
收藏
页码:3701 / 3707
页数:7
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