## Abstract The extent and modes of binding of the divalent metal ions Mn^2+^ and Co^2+^ to DNA and the effects of salt on the binding have been studied by measurements of the effects of these paramagnetic metal ions on the longitudinal and transverse relaxation rates of the protons of the solvent
Interaction of Mn2+ with DNA as studied by proton-relaxation enhancement of solvent water
✍ Scribed by Raymond Van Steenwinkel; Francesco Campagnari; Margaret Merlini
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1981
- Tongue
- English
- Weight
- 489 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0006-3525
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✦ Synopsis
Abstract
The binding of Mn^2+^ to double‐stranded DNA in solution has been studied by measuring the proton‐relaxation enhancement of solvent water. The nmr experiments were carried out on DNAs of different base composition and showed the existence of weak and tight binding sites for Mn^2+^. The former sites are related to the electrostatic binding of the divalent cation with two contiguous phosphate groups, and the latter appear to vary almost proportionally with the number of G·C base pairs in the DNAs. Our results agree, in general, with the emerging evidence for a specific interaction of Mn^2+^ with the G·C residues of DNA. Competition experiments with Mg^2+^ suggested that this binding of Mn^2+^ in DNA also involves the phosphate groups. More definitely, our data conform with the hypothesis made by Clement et al. of Mn^2+^ chelation between the phosphate and the nitrogen N7 of a deoxyguanyl unit of DNA.
📜 SIMILAR VOLUMES
Proton and phosphorus-31 nuclear spin-lattice relaxation times 2' 1 and spin-spin relaxation times T2 have been measured on the single-stranded polyriboadenylic acid [poly(A)]-Mn2+ system in a neutral D2O solution in the temperature range 10"-90"C a t 100 and 40.5 MHz, respectively, with the Fourier