Monofunctional adducts of platinum(II) produce in DNA a sequence-dependent local denaturation
Language English Country United States Media print
Document type Journal Article
PubMed
8312249
DOI
10.1021/bi00172a005
Knihovny.cz E-resources
- MeSH
- Acetaldehyde analogs & derivatives metabolism MeSH
- Cisplatin analogs & derivatives pharmacology MeSH
- Nucleic Acid Denaturation drug effects MeSH
- DNA chemistry metabolism MeSH
- Enzyme-Linked Immunosorbent Assay MeSH
- Spectrometry, Fluorescence MeSH
- Transcription, Genetic MeSH
- Nucleic Acid Conformation drug effects MeSH
- Chromosome Mapping MeSH
- Molecular Sequence Data MeSH
- Piperidines metabolism MeSH
- Deoxyribonucleases, Type II Site-Specific MeSH
- Base Sequence MeSH
- Hydrogen Bonding MeSH
- Base Composition MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Acetaldehyde MeSH
- chloroacetaldehyde MeSH Browser
- chlorodiethylenetriamine platinum MeSH Browser
- Cisplatin MeSH
- diamminemonoaquamonochloroplatinum(II) MeSH Browser
- DNA MeSH
- endodeoxyribonuclease HpaI MeSH Browser
- endodeoxyribonuclease NdeI MeSH Browser
- piperidine MeSH Browser
- Piperidines MeSH
- Deoxyribonucleases, Type II Site-Specific MeSH
The effects on the conformation of DNA produced by the monofunctional adducts of chloro-(diethylenetriamine)platinum(II) chloride or cis-diamminemonoaquamonochloroplatinum(II) have been investigated by means of the single-strand-specific probe chloroacetaldehyde (CAA). The denatured sites to which CAA was bound and that were induced in DNA by the monofunctional adducts of the platinum complexes were characterized by means of three experimental approaches. These include measurement of the fluorescence of a plasmid fragment treated with CAA, analysis of oligonucleotides treated with CAA and cleaved by piperidine, and termination of duplex transcription on a fragment of plasmid DNA treated with CAA. The results indicate that the denaturational change preferentially occurs in the base pair containing the monoadducted deoxyriboguanosine in the trinucleotide sequence Py-deoxyriboguanosine-Py (Py is a pyrimidine deoxyribonucleoside). It was suggested that this conformational alteration facilitates in DNA the formation of minor bifunctional adducts of cis-diamminedichloroplatinum(II).
References provided by Crossref.org
DNA interactions of antitumor cisplatin analogs containing enantiomeric amine ligands