Literature DB >> 6194816

Interaction of bleomycin A2 with poly(deoxyadenylylthymidylic acid). A proton nuclear magnetic resonance study of the influence of temperature, pH, and ionic strength.

T E Booth, T T Sakai, J D Glickson.   

Abstract

The binding of bleomycin A2 to poly(deoxyadenylylthymidylic acid) [poly(dA-dT)] has been monitored by proton nuclear magnetic resonance spectroscopy. This study includes an analysis of the effects of temperature, ionic strength, and pH. Sites of drug-nucleic acid interaction have been delineated on the basis of chemical shift perturbations of drug and nucleic acid resonances. The data indicate that the binding of the antibiotic occurs with partial intercalation of the aromatic bithiazole group and immobilization of the cationic dimethylsulfonium group. This complex dissociates as the nucleic acid is denatured to the single-stranded form. The absence of significant pH effects suggests that the N terminus of bleomycin A2, which contains the titratable groups, does not contribute to the interaction of the drug molecule with poly(dA-dT). The problems associated with assigning a specific geometry to the drug-nucleic acid complex are discussed.

Entities:  

Mesh:

Substances:

Year:  1983        PMID: 6194816     DOI: 10.1021/bi00287a008

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  2 in total

1.  Is the bithiazole moiety of bleomycin a classical intercalator?

Authors:  J P Hénichart; J L Bernier; N Helbecque; R Houssin
Journal:  Nucleic Acids Res       Date:  1985-09-25       Impact factor: 16.971

Review 2.  Contributions of NMR to the understanding of the coordination chemistry and DNA interactions of metallo-bleomycins.

Authors:  Teresa Lehmann; Elena Topchiy
Journal:  Molecules       Date:  2013-08-02       Impact factor: 4.411

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.