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Fernandes, A., Viterisi, A., Aucagne, V., Leigh, D.A. and Papot, S.

Second generation specific-enzyme-activated rotaxane propeptides

Chemical Communications 48 (15) 2083-2085

par Frapart - publié le , mis à jour le

Abstract :

A [2]rotaxane, in which the peptidic axle is protected from degradation by the macrocyclic sheath and terminated with a novel glycosidase-cleavable stopper, is rendered water-soluble by derivatisation with tetra(ethylene glycol) (TetEG) or glucosylated tetra(ethylene glycol) (Glc-TetEG) chains using the CuAAC ’click’ reaction. The Glc-TetEG-derivatised rotaxane propeptide is >50 000 times more soluble in aqueous media than the parent rotaxane. Activation of the water-soluble rotaxane propeptide with a β-galactosidase efficiently releases the parent peptide.