Azabicyclic vinyl sulfones for residue-specific dual protein labelling. Issue 16 (26th March 2019)

• Record Type: Journal Article
• Authors: Gil de Montes, Enrique; Jiménez-Moreno, Ester; Oliveira, Bruno L.; Navo, Claudio D.; Cal, Pedro M. S. D.; Jiménez-Osés, Gonzalo; Robina, Inmaculada; Moreno-Vargas, Antonio J.; Bernardes, Gonçalo J. L.
• Is Part Of: Chemical science. Volume 10:Issue 16(2019)
• Page Start: 4515
• Page End: 4522
• Publication Date: 2019-03-26
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c9sc00125e
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : We have developed [2.2.1]azabicyclic vinyl sulfone reagents that simultaneously enable cysteine-selective protein modification and introduce a handle for further bioorthogonal ligation. Abstract : We have developed [2.2.1]azabicyclic vinyl sulfone reagents that simultaneously enable cysteine-selective protein modification and introduce a handle for further bioorthogonal ligation. The reaction is fast and selective for cysteine relative to other amino acids that have nucleophilic side-chains, and the formed products are stable in human plasma and are moderately resistant to retro Diels–Alder degradation reactions. A model biotinylated [2.2.1]azabicyclic vinyl sulfone reagent was shown to efficiently label two cysteine-tagged proteins, ubiquitin and C2Am, under mild conditions (1–5 equiv. of reagent in NaPi pH 7.0, room temperature, 30 min). The resulting thioether-linked conjugates were stable and retained the native activity of the proteins. Finally, the dienophile present in the azabicyclic moiety on a functionalised C2Am protein could be fluorescently labelled through an inverse electron demand Diels–Alder reaction in cells to allow selective apoptosis imaging. The combined advantages of directness, site-specificity and easy preparation mean [2.2.1]azabicyclic vinyl sulfones can be used for residue-specific dual protein labelling/construction strategies with minimal perturbation of native function based simply on the attachment of an [2.2.1]azabicyclic moiety to cysteine.