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Oligonucleotides Incorporating Palladacyclic Nucleobase Surrogates




TekijätMaity SK, Lonnberg T

KustantajaWILEY-V C H VERLAG GMBH

Julkaisuvuosi2018

JournalChemistry - A European Journal

Tietokannassa oleva lehden nimiCHEMISTRY-A EUROPEAN JOURNAL

Lehden akronyymiCHEM-EUR J

Vuosikerta24

Numero6

Aloitussivu1274

Lopetussivu1277

Sivujen määrä4

ISSN0947-6539

DOIhttps://doi.org/10.1002/chem.201705797

Rinnakkaistallenteen osoitehttps://research.utu.fi/converis/portal/detail/Publication/30491162


Tiivistelmä
An oligonucleotide incorporating a palladacyclic nucleobase has been prepared by ligand-directed metalation of a phenylpyridine moiety. This oligonucleotide hybridized with natural counterparts placing any of the canonical nucleobases opposite to the palladacyclic residue. The palladated duplexes had B-type conformation and melting temperatures comparable to those of respective unmodified duplexes with a single mismatch. In the duplexes placing C, G or T (but not A) opposite to the palladacyclic residue, greatly increased absorptivity suggested formation of a Pd-II-mediated base pair. Absorptivity and ellipticity of these duplexes persisted even at the highest temperatures applicable in T-m and CD experiments (90 degrees C). Evidently the Pd-II-mediated base pairs do not dissociate under the experimental conditions.

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