DNA binding of Pd(TC3), a conformable cationic porphyrin with a long-lived triplet state

July 28, 2017

Title

DNA binding of Pd(TC3), a conformable cationic porphyrin with a long-lived triplet state

Author

Srijana Ghimire, Matthew A. Bork, Hanyu Zhang, Phillip E. Fanwick, Matthias Zeller, Jong Hyun Choi, David R. McMillin

Year

2016

Journal

Dalton Transactions

Abstract

The goal of this work has been to synthesize and investigate Pd(TC3), an intercalating porphyrin that has conformable substituents capable of groove binding to B-form DNA. (TC3 denotes the doubly deprotonated form of 5,10,15,20-tetra[3-(3′-methylimidazolium-1′-yl)prop-1-yl]porphyrin.) Palladium(II) is an apt choice for the central metal ion because it remains strictly four-coordinate and provides for a luminescent triplet excited state with a long lifetime. The DNA hosts are hairpin-forming sequences programmed to differ in base composition. Luminescence, absorbance, and circular dichroism results are consistent with the idea that congruent structural reorganization takes place at the host and ligand during uptake. Photoexcitation of DNA-bound Pd(TC3) generates a comparatively modest steady state concentration of singlet oxygen, due to a relatively slow reaction with molecular oxygen in solution. The sheer size of the substituent groups disfavors quenching, but groove-binding interactions compound the problem by inhibiting mobility. The results show how ligand design affects adduct structure as well as function.

Instrument

J-810

Keywords

Circular dichroism, DNA structure, Ligand binding, Coordination chemistry, Biochemistry