Circular dichroism spectroscopy of a cationic porphyrin bound to DNA

Recently, the porphyrin photosensitizer meso-tetra(4-N-methyl-pyridyl)-porphine was identified as a DNA-reactive agent demonstrating both electrostatic and intercalative binding. A series of porphyrin derivatives were synthesized and studied to see if similar compounds manifested identical behavior....

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Veröffentlicht in:Biochemical and biophysical research communications 1982-09, Vol.108 (1), p.66-73
Hauptverfasser: Carvlin, Mark J., Datta-Gupta, Nirmalendu, Fiel, Robert J.
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container_title Biochemical and biophysical research communications
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creator Carvlin, Mark J.
Datta-Gupta, Nirmalendu
Fiel, Robert J.
description Recently, the porphyrin photosensitizer meso-tetra(4-N-methyl-pyridyl)-porphine was identified as a DNA-reactive agent demonstrating both electrostatic and intercalative binding. A series of porphyrin derivatives were synthesized and studied to see if similar compounds manifested identical behavior. One derivative, meso-tetra(p-N-trimethylanilinium) porphine did not exhibit intercalation behavior but did show avid binding and novel circular dichroic features when bound to B-form DNA. At an ionic strength of 1.02, the binding constant was found to be on the order of 10 4 and higher at lower ionic strength. The large binding constants and induced optical activity suggest that at large porphyrin/DNA ratios the final porphyrin · DNA complex may take the form of a suprahelical helix.
doi_str_mv 10.1016/0006-291X(82)91832-0
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subjects Animals
Cattle
Circular Dichroism
DNA
Kinetics
Mesoporphyrins
Models, Molecular
Nucleic Acid Conformation
Porphyrins
Thymus Gland
title Circular dichroism spectroscopy of a cationic porphyrin bound to DNA
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