4.4 Article

The binding mode of porphyrins with cation side arms to (TG4T)4 G-quadruplex: Spectroscopic evidence

Journal

BIOPHYSICAL CHEMISTRY
Volume 143, Issue 1-2, Pages 79-84

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.bpc.2009.04.005

Keywords

Binding modes; G-quadruplexes; Interaction; Porphyrin; Spectroscopy

Funding

  1. National Natural Science Foundation of China [20503029, 20673110]
  2. Natural Science Fund of Shanxi Province [2009011012-2]
  3. Scientific Research Foundation for the Returned Overseas Chinese Scholars of Shanxi Province

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Interactions of 5,10,15,20-Tetrakis(N-methylpyridinium-4-yl)-21H,23H-porphyrin (TMPyP4) and 5,10,15,20-Tetrakis(N-propylpyridinium-4-yl)-21H,23H-porphyrin (TPrPyP4) with the parallel four-stranded (TG(4)T)4 G-quadruplex DNA in 100 mM K+-containing buffer were studied using circular dichroism (CD) spectroscopy, visible absorption titration, and steady and time-resolved fluorescence spectroscopies. The results show that the binding stoichiometric ratios of both TMPyP4 and TPrPyP4 to (TG(4)T)4 are 3:1. Two types of independent and nonequivalent binding sites with the higher and lower binding affinities are confirmed, and the stronger and weaker binding constants are 9.44 x 10(7) and 6.94 x 10(5) M-1 for (TG(4)T)4-TMPyP4 complex, 7.86 x 10(7) and 6.35 x 10(5) M-1 for (TG(4)T)4-TPrPyP4 complex, respectively. For both TMPyP4-(TG(4)T)4 and TPrPyP4-(TG(4)T)4 complexes, one porphyrin molecule stacks on the one end of G-quadruplex with the higher binding affinity, another two porphyrins bind weakly to the two external grooves. The size of cation side arms around porphyrin core almost fails to affect the binding mode, stoichiometry and affinity of porphyrin to (TG(4)T)4 G-quadruplex in 100 mM K+-containing buffer. (C) 2009 Elsevier B.V. All rights reserved.

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