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Identification of potential cellular targets of aloisine A by affinity chromatography.
Corbel C., Haddoub R., Guiffant D., Lozach O., Gueyrard D., Lemoine J., Ratin M., Meijer L., Bach S., Goekjian P.
Bioorg Med Chem 17, 15 (2009) 5572-82 - http://hal.archives-ouvertes.fr/hal-00416033
Articles dans des revues avec comité de lecture
Sciences du Vivant/Biologie cellulaire
Identification of potential cellular targets of aloisine A by affinity chromatography.
Caroline Corbel 1, Rose Haddoub, Damien Guiffant, Olivier Lozach 2, David Gueyrard, Jérôme Lemoine 3, Morgane Ratin, Laurent Meijer 2, Stéphane Bach, Peter Goekjian 4
1 :  Laboratoire des Solides Irradiés (LSI)
http://www.lsi.polytechnique.fr
CNRS : UMR7642 – Polytechnique - X – CEA : DSM/IRAMIS
28 route de Saclay 91128 Palaiseau Cedex
France
2 :  Molécules et cibles thérapeutiques (MCT)
CNRS : UPS2682
Station biologique Place Georges Teissier - BP 74 29682 ROSCOFF CEDEX
France
3 :  Dynamique terrestre et planétaire (DTP)
http://www.obs-mip.fr/omp/umr5562/
CNRS : UMR5562 – Observatoire Midi-Pyrénées – INSU – Université Paul Sabatier [UPS] - Toulouse III
14 Av Edouard Belin 31400 TOULOUSE
France
4 :  inconnu
Inconnu
France
Affinity chromatography was used to identify potential cellular targets of aloisine A (7-n-butyl-6-(4'-hydroxyphenyl)-5H-pyrrolo[2,3b]pyrazine), a potent inhibitor of cyclin-dependent kinases. This technique is based on the immobilization of the drug on a solid matrix, followed by identification of specifically bound proteins. To this end, both aloisine A and the protein-kinase inactive control N-methyl aloisine, bearing extended linker chains have been synthesized. We present the preparation of such analogues having the triethylene glycol chain at different positions of the molecule, as well as their immobilization on an agarose-based matrix. Affinity chromatography of various biological extracts on the aloisine matrices allowed the identification of both protein kinases and non-kinase proteins as potential cellular targets of aloisine.
Anglais

Bioorg Med Chem
internationale
01/08/2009
18/06/2009
17
15
5572-82