Protected 32P‐Labels in Deoxyribonucleotides: Investigation of Sequence Selectivity of DNA Photocleavage by Enediyne–, Fulvene–, and Acetylene–Lysine Conjugates

Finding a compromise: The sequence selectivity of DNA photocleavage by enediyne–, acetylene–, and fulvene–lysine conjugates was investigated by using labeled DNA oligomers. Since the external 32P label was removed by these photocleavers, the label was protected by translocation inside the oligomer (...

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Veröffentlicht in:Angewandte Chemie International Edition 2006-05, Vol.45 (22), p.3666-3670
Hauptverfasser: Breiner, Boris, Schlatterer, Jörg C., Kovalenko, Serguei V., Greenbaum, Nancy L., Alabugin, Igor V.
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container_title Angewandte Chemie International Edition
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creator Breiner, Boris
Schlatterer, Jörg C.
Kovalenko, Serguei V.
Greenbaum, Nancy L.
Alabugin, Igor V.
description Finding a compromise: The sequence selectivity of DNA photocleavage by enediyne–, acetylene–, and fulvene–lysine conjugates was investigated by using labeled DNA oligomers. Since the external 32P label was removed by these photocleavers, the label was protected by translocation inside the oligomer (see figure). The selectivity of cleavage is controlled by a compromise between AT selectivity for binding and G selectivity for electron transfer.
doi_str_mv 10.1002/anie.200504479
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Acetylene - chemistry
alkynes
Cyclopentanes - chemistry
Deoxyribonucleotides - chemistry
DNA - chemistry
DNA Cleavage
electron transfer
Enediynes - chemistry
fulvenes
Lysine - chemistry
Phosphorus Radioisotopes - chemistry
Photochemistry
title Protected 32P‐Labels in Deoxyribonucleotides: Investigation of Sequence Selectivity of DNA Photocleavage by Enediyne–, Fulvene–, and Acetylene–Lysine Conjugates
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