Formation of i-motifs from acyclic (l)-threoninol nucleic acids.


Journal

Organic & biomolecular chemistry
ISSN: 1477-0539
Titre abrégé: Org Biomol Chem
Pays: England
ID NLM: 101154995

Informations de publication

Date de publication:
07 09 2019
Historique:
pubmed: 31 7 2019
medline: 6 2 2020
entrez: 31 7 2019
Statut: ppublish

Résumé

Acyclic (l)-threoninol nucleic acids ((l)-aTNA) containing poly-cytosines are prepared and investigated at various pH values, revealing the formation of a highly stable structure at lower pH that have the characteristics of an i-motif. Depending on the sequence, the aTNA forms inter-, bi- and intra-molecular i-motif structures. Pyrene was conjugated to aTNA sequences and both monomeric and excimer fluorescence were efficiently quenched by the i-motif structures and thus demonstrated that the aTNA i-motif can serve as a pH switch.

Identifiants

pubmed: 31360984
doi: 10.1039/c9ob01220f
doi:

Substances chimiques

Amino Alcohols 0
Butylene Glycols 0
Nucleic Acids 0
threoninol 0
Poly C 30811-80-4

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

7655-7659

Auteurs

Vipin Kumar (V)

Center for Multifunctional Biomolecular Drug Design (CEMBID), iNANO and Department of Chemistry, Aarhus University, 8000 Aarhus C, Denmark. kvg@chem.au.dk.

Thuy J D Nguyen (TJD)

Center for Multifunctional Biomolecular Drug Design (CEMBID), iNANO and Department of Chemistry, Aarhus University, 8000 Aarhus C, Denmark. kvg@chem.au.dk.

Johan Palmfeldt (J)

Department of Clinical Medicine - Research Unit for Molecular Medicine Aarhus University, 8200 Aarhus N, Denmark.

Kurt V Gothelf (KV)

Center for Multifunctional Biomolecular Drug Design (CEMBID), iNANO and Department of Chemistry, Aarhus University, 8000 Aarhus C, Denmark. kvg@chem.au.dk.

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Classifications MeSH