The nature of calf thymus DNA in aqueous solution, in the presence of the organotin(IV) species Sn(IV)Me3, Sn(IV)Me2 and Sn(IV)Me, possibly partly hydrolysed and/or hydrated, was investigated by small-angle X-ray scattering (SAXS), ultraviolet spectroscopy (UV) at different temperatures and circular dichroism (CD). The results are compared with those of previous 119Sn Mossbauer studies on condensed DNA phases. The effects of tin-phosphate oxygen bonding on the DNA melting profile in DNA-Sn(IV)Me systems are in agreement with previous reports on DNA-Main Group metal ion interactions. The structure and conformation of the DNA double helix are not influenced by Sn(IV)Me(n) species, even in experimental conditions near the onset of DNA condensation. Gel electrophoresis indicates that DNA is not degraded by Sn(IV)Me(n); the X-ray radii of gyration of the DNA cross-section and its mass per unit length, determined by SAXS from aqueous solutions, are constant and independent of the nature and concentration of the Sn(IV)Me(n) species present in the solutions. The invariance of the interparticle distances in solution at very low ionic strengths, in the presence of increasing amounts of Sn(IV)Me(n) compounds, even approaching DNA precipitation, suggests that the condensation process involves isolated DNA chains. Copyright (C) 2000 John Wiley and Sons, Ltd.

Barone G., Barbieri R., La Manna G., Koch M.H.J. (2000). The interaction of deoxyribonucleic acid with methyltin(IV) moieties in solution studied by small-angle X-ray scattering, circular dichroism and UV spectroscopy. APPLIED ORGANOMETALLIC CHEMISTRY, 14(4), 189-196 [10.1002/(SICI)1099-0739(200004)14:4<189::AID-AOC975>3.0.CO;2-F].

The interaction of deoxyribonucleic acid with methyltin(IV) moieties in solution studied by small-angle X-ray scattering, circular dichroism and UV spectroscopy

Barone G.;Barbieri R.
;
La Manna G.;
2000-01-01

Abstract

The nature of calf thymus DNA in aqueous solution, in the presence of the organotin(IV) species Sn(IV)Me3, Sn(IV)Me2 and Sn(IV)Me, possibly partly hydrolysed and/or hydrated, was investigated by small-angle X-ray scattering (SAXS), ultraviolet spectroscopy (UV) at different temperatures and circular dichroism (CD). The results are compared with those of previous 119Sn Mossbauer studies on condensed DNA phases. The effects of tin-phosphate oxygen bonding on the DNA melting profile in DNA-Sn(IV)Me systems are in agreement with previous reports on DNA-Main Group metal ion interactions. The structure and conformation of the DNA double helix are not influenced by Sn(IV)Me(n) species, even in experimental conditions near the onset of DNA condensation. Gel electrophoresis indicates that DNA is not degraded by Sn(IV)Me(n); the X-ray radii of gyration of the DNA cross-section and its mass per unit length, determined by SAXS from aqueous solutions, are constant and independent of the nature and concentration of the Sn(IV)Me(n) species present in the solutions. The invariance of the interparticle distances in solution at very low ionic strengths, in the presence of increasing amounts of Sn(IV)Me(n) compounds, even approaching DNA precipitation, suggests that the condensation process involves isolated DNA chains. Copyright (C) 2000 John Wiley and Sons, Ltd.
2000
Barone G., Barbieri R., La Manna G., Koch M.H.J. (2000). The interaction of deoxyribonucleic acid with methyltin(IV) moieties in solution studied by small-angle X-ray scattering, circular dichroism and UV spectroscopy. APPLIED ORGANOMETALLIC CHEMISTRY, 14(4), 189-196 [10.1002/(SICI)1099-0739(200004)14:4<189::AID-AOC975>3.0.CO;2-F].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10447/513792
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