Flavin Conjugates for Delivery of Peptide Nucleic Acids

F. Marlin, , P. Simon, , S. Bonneau , P. Alberti, , C. Cordier, , C. Boix, , L. Perrouault, , A. Fossey, , T. Saison-Behmoaras, , M. Fontecave, , C. Giovannangeli,

Bibtex , URL
ChemBioChem, 13, 17, 2593-2598
Published 26 Nov. 2012
DOI: 10.1002/cbic.201200505
ISSN: 1439-4227


Oligonucleotides and their analogues, such as peptide nucleic acids (PNAs), can be used in chemical strategies to artificially control gene expression. Inefficient cellular uptake and inappropriate cellular localization still remain obstacles in biological applications, however, especially for PNAs. Here we demonstrate that conjugation of PNAs to flavin resulted in efficient internalization into cells through an endocytic pathway. The flavinPNAs exhibited antisense activity in the sub-micromolar range, in the context of a treatment facilitating endosomal escape. Increased endosomal release of flavin conjugates into the cytoplasm and/or nucleus was shown by chloroquine treatment and alsowhen the flavinPNA was conjugated to rhodamine, a mild photosensitizerupon light irradiation. In conclusion, an isoalloxazine moiety can be used as a carrier and attached to a cargo biomolecule, here a PNA, for internalization and functional cytoplasmic/nuclear delivery. Our findings could be useful for further design of PNAs and other oligonucleotide analogues as potent antisense agents.

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