Synthesis of nucleosides and dNTPs bearing oligopyridine ligands linked through an octadiyne tether, their incorporation into DNA and complexation with transition metal cations
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
23090069
DOI
10.1039/c2ob26881g
Knihovny.cz E-zdroje
- MeSH
- alkyny chemie MeSH
- DNA chemie MeSH
- kationty chemie MeSH
- ligandy MeSH
- molekulární struktura MeSH
- nukleosidy chemická syntéza chemie MeSH
- organokovové sloučeniny chemická syntéza chemie MeSH
- polyfosfáty chemická syntéza chemie MeSH
- přechodné kovy chemie MeSH
- pyridiny chemie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- alkyny MeSH
- DNA MeSH
- kationty MeSH
- ligandy MeSH
- nukleosidy MeSH
- organokovové sloučeniny MeSH
- polyfosfáty MeSH
- přechodné kovy MeSH
- pyridiny MeSH
- triphosphoric acid MeSH Prohlížeč
Modified nucleosides (dA(R)s and dC(R)s) bearing bipyridine or terpyridine ligands attached through an octadiyne linker were prepared by single-step aqueous-phase Sonogashira cross-coupling of 7-iodo-7-deaza-2'-deoxyadenosine and 5-iodo-2'-deoxycytidine with the corresponding bipyridine- or terpyridine-octadiynes and were triphosphorylated to the corresponding nucleoside triphosphates (dA(R)TPs and dC(R)TPs). The modified dN(R)TPs were successfully incorporated into the oligonucleotides by primer extension experiment (PEX) using different DNA polymerases and the PEX products were used for post-synthetic complexation with divalent metal cations. The complexation of these DNAs containing flexibly-tethered ligands was compared with the previously reported ones bearing rigid acetylene-linked ligands suggesting the possible formation of both inter- and intra-strand complexes with Ni(2+) or Fe(2+).
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