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

被引:0
作者
Barone, G
Barbieri, R
La Manna, G
Koch, MHJ
机构
[1] Univ Palermo, Dipartimento Chim Inorgan, I-90128 Palermo, Italy
[2] Univ Palermo, Dipartimento Chim Fis, I-90128 Palermo, Italy
[3] DESY, European Mol Biol Lab, Hamburg Outstn, D-22603 Hamburg, Germany
关键词
DNA; organotin; structure; spectroscopy;
D O I
10.1002/(SICI)1099-0739(200004)14:4<189::AID-AOC975>3.0.CO;2-F
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The nature of calf thymus DNA in aqueous solution, in the presence of the organotin(IV) species (SnMe3)-Me-IV, (SnMe2)-Me-IV and Snn(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 Sn-119 Mossbauer studies on condensed DNA phases. The effects of tin-phosphate oxygen bonding on the DNA melting profile in DNA-(SnMe)-Me-IV 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 (SnMen)-Me-IV species, even in experimental conditions near the onset of DNA condensation. Gel electrophoresis indicates that DNA is not degraded by (SnMen)-Me-IV; 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 (SnMen)-Me-IV 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 (SnMen)-Me-IV compounds, even approaching DNA precipitation, suggests that the condensation process involves isolated DNA chains, Copyright (C) 2000 John Wiley & Sons, Ltd.
引用
收藏
页码:189 / 196
页数:8
相关论文
共 61 条
[1]  
[Anonymous], ORGANOMETALLIC COMPO
[2]   THERMODYNAMICS OF HYDROXO COMPLEX-FORMATION OF DIALKYLTIN(IV) IONS IN AQUEOUS-SOLUTION [J].
ARENA, G ;
PURRELLO, R ;
RIZZARELLI, E ;
GIANGUZZA, A ;
PELLERITO, L .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1989, (05) :773-777
[3]   SN-119 MOSSBAUER TITRATION OF DIMETHYL-TIN(IV) AND TRIMETHYL-TIN(IV) HYDROXIDES WITH MODEL LIGANDS MIMICKING NUCLEIC-ACID PHOSPHATE SITES, AND WITH DEOXYRIBONUCLEIC-ACID [J].
BARBIERI, R ;
SILVESTRI, A ;
PIRO, V .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1990, (12) :3605-3609
[4]   DYNAMICS OF TIN NUCLEI IN ALKYLTIN(IV) DEOXYRIBONUCLEIC-ACID CONDENSATES BY VARIABLE-TEMPERATURE SN-119 MOSSBAUER-SPECTROSCOPY [J].
BARBIERI, R ;
RUISI, G ;
SILVESTRI, A ;
GIULIANI, AM ;
BARBIERI, A ;
SPINA, G ;
PIERALLI, F ;
DELGIALLO, F .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1995, (03) :467-475
[5]   THE CONFIGURATION AND LATTICE-DYNAMICS OF COMPLEXES OF DIALKYLTIN(IV) WITH ADENOSINE 5'-MONOPHOSPHATE AND PHENYL PHOSPHATES [J].
BARBIERI, R ;
ALONZO, G ;
HERBER, RH .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1987, (04) :789-794
[6]   THE INTERACTION OF NATIVE DNA WITH DIMETHYLTIN(IV) SPECIES [J].
BARBIERI, R ;
SILVESTRI, A .
JOURNAL OF INORGANIC BIOCHEMISTRY, 1991, 41 (01) :31-35
[7]   ORGANOTIN COMPOUNDS AND DEOXYRIBONUCLEIC-ACID [J].
BARBIERI, R ;
SILVESTRI, A ;
GIULIANI, AM ;
PIRO, V ;
DISIMONE, F ;
MADONIA, G .
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS, 1992, (04) :585-590
[8]  
BARBIERI R, 1998, CHEM TIN, P496
[9]  
BARONE C, 1997, THESIS U PALERMO
[10]   Semiempirical calculations on the interaction between dimethyltin(IV) and DNA model system [J].
Barone, G ;
Ramusino, MC ;
Barbieri, R ;
La Manna, G .
JOURNAL OF MOLECULAR STRUCTURE-THEOCHEM, 1999, 469 :143-149