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pubmed-article:10808407pubmed:abstractTextThe cobalt(II) tetracarboxyphthalocyanine-deoxyribonucleotide pd(TCTTCCCA) conjugate was synthesized. The phthalocyanine N-succinimide ester prepared from phthalocyanine using DCC was mixed in DMF with an aqueous solution of the oligonucleotide bearing a 1,3-diaminopropane linker at the 5'-phosphate. The resulting conjugate was tested in the intraduplex reaction with target 14-mer and 22-mer oligonucleotides containing conjugate-complementary sequences. In the presence of O2 and a thiol (2-mercaptoethanol or DTT) as a coupled reducer or H2O2, sequence-specific DNA modification was observed that caused the cleavage of the target upon treatment with piperidine.lld:pubmed
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pubmed-article:10808407pubmed:authorpubmed-author:Koval'V VVVlld:pubmed
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pubmed-article:10808407pubmed:volume26lld:pubmed
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pubmed-article:10808407pubmed:pagination118-25lld:pubmed
pubmed-article:10808407pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:10808407pubmed:articleTitle[The synthesis of a cobalt(II) tetracarboxyphthalocyanine- deoxyribooligonucleotide conjugate as a reagent for the directed DNA modification].lld:pubmed
pubmed-article:10808407pubmed:affiliationNovosibirsk Institute of Bioorganic Chemistry, Siberian Division, Russian Academy of Sciences, Russia.lld:pubmed
pubmed-article:10808407pubmed:publicationTypeJournal Articlelld:pubmed
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