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Issue 39, 2013
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Synthesis and binding of proflavine diazides as functional intercalators for directed assembly on DNA

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Abstract

Proflavine diazide (PD) with amido-azide substituents on the amine groups and its N-methylated analogue (MePD) bind strongly to DNA by nearest-neighbour intercalation with little sequence selectivity, presenting reactive azide groups in the major groove. PD is neutral in aqueous solution but experiences binding-coupled protonation on interaction with DNA with an apparent pKa shift of 2.5 units. MePD can be click modified in situ on DNA with alkyne-functionalised thienyl-pyrrole as a precursor for conducting polymer synthesis, and remains intercalated after reaction with the substituents aligned in the groove.

Graphical abstract: Synthesis and binding of proflavine diazides as functional intercalators for directed assembly on DNA

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Publication details

The article was received on 09 Apr 2013, accepted on 09 Jul 2013 and first published on 12 Jul 2013


Article type: Paper
DOI: 10.1039/C3RA43090A
Citation: RSC Adv., 2013,3, 18164-18172
  • Open access: Creative Commons BY license
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    Synthesis and binding of proflavine diazides as functional intercalators for directed assembly on DNA

    S. MoradpourHafshejani, J. H. Hedley, A. O. Haigh, A. R. Pike and E. M. Tuite, RSC Adv., 2013, 3, 18164
    DOI: 10.1039/C3RA43090A

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