Published online 14 February 2006
Methods Online |
Diels-Alder cycloadditions in water for the straightforward preparation of peptideoligonucleotide conjugates
Departament de Química Orgànica, Facultat de Química, Universitat de Barcelona Martí i Franquès 1-11, E-08028 Barcelona, Spain
*To whom correspondence should be addressed. Tel: +34 93 402 12 63; Fax: +34 93 339 78 78; Email: anna.grandas{at}ub.edu
Received November 18, 2005. Revised December 16, 2005. Accepted January 19, 2006.
The Diels-Alder reaction between diene-modified oligonucleotides and maleimide-derivatized peptides afforded peptideoligonucleotide conjugates with high purity and yield. Synthesis of the reagents was easily accomplished by on-column derivatization of the corresponding peptides and oligonucleotides. The cycloaddition reaction was carried out in mild conditions, in aqueous solution at 37°C. The speed of the reaction was found to vary depending on the size of the reagents, but it can be completed in 810 h by reacting the diene-oligonucleotide with a small excess of maleimide-peptide.
Correspondence may also be addressed to Vicente Marchán. Tel: +34 93 402 12 49; Fax: +34 93 339 78 78; Email: vmarchan{at}ub.edu
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
V. Borsenberger and S. Howorka Diene-modified nucleotides for the Diels-Alder-mediated functional tagging of DNA Nucleic Acids Res., April 1, 2009; 37(5): 1477 - 1485. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Gogoi, M. V. Mane, S. S. Kunte, and V. A. Kumar A versatile method for the preparation of conjugates of peptides with DNA/PNA/analog by employing chemo-selective click reaction in water Nucleic Acids Res., December 18, 2007; 35(21): e139 - e139. [Abstract] [Full Text] [PDF] |
||||
