| Literature DB >> 22227715 |
Antony Fernandes1, Aurélien Viterisi, Vincent Aucagne, David A Leigh, Sébastien Papot.
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. This journal is © The Royal Society of Chemistry 2012Entities:
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Year: 2012 PMID: 22227715 DOI: 10.1039/c2cc17458h
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222