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Shows stronger binding of porphyrins to cancer DNA in acidic conditions, indicating targeted therapy potential.
High Resolution Image Download MS PowerPoint Slide The affinities of porphyrins to healthy and cancer DNA under physiological and acidic conditions were studied. Titration of meso -tetra(4- N -hydroxyethylpyridyl)porphyrin and its Ag-substituted derivative solutions with DNAs, isolated from healthy and tumor tissues, has been performed. Using the simple neighbor-exclusion model of McGhee and von Hippel with the binding isotherm formula optimized for fitting errors, we found the binding constant K b and exclusion parameter n from the titration absorption spectra. It was shown that the binding parameters of porphyrins to DNA under acidic conditions are higher than those under physiological conditions. The K b of porphyrins with cancer DNA at pH 6.4 is an order of magnitude higher, and n is lower than that of healthy DNA at pH 7.4. The enhanced affinity of porphyrins for cancer DNA indicates that conformational alterations in the DNA structure create more-accessible binding sites. This selective interaction underscores the potential of porphyrins as effective agents for a targeted anticancer therapy.
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Karapetyan et al. (2026) studied this question.
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