Glutathione Mediates Control of Dual Differential Bio‐orthogonal Labelling of Biomolecules

Abstract: Traditional approaches to bio‐orthogonal reaction discovery have focused on developing reagent pairs that react with each other faster than they are metabolically degraded. Glutathione (GSH) is typically responsible for the deactivation of most bio‐orthogonal reagents. Here we demonstrate that GSH promotes a Cu‐catalysed (3+2) cycloaddition reaction between an ynamine and an azide. We show that GSH acts as a redox modulator to control the Cu oxidation state in these cycloadditions. Rate enhancement of this reaction is specific for ynamine substrates and is tuneable by the Cu:GSH ratio. This unique GSH‐mediated reactivity gradient is then utilised in the dual sequential bio‐orthogonal labelling of peptides and oligonucleotides via two distinct chemoselective (3+2) cycloadditions.

Standort
Deutsche Nationalbibliothek Frankfurt am Main
Umfang
Online-Ressource
Sprache
Englisch

Erschienen in
Glutathione Mediates Control of Dual Differential Bio‐orthogonal Labelling of Biomolecules ; day:13 ; month:11 ; year:2023 ; extent:11
Angewandte Chemie / International edition. International edition ; (13.11.2023) (gesamt 11)

Urheber
Peschke, Frederik
Taladriz‐Sender, Andrea
Andrews, Matthew J.
Watson, Allan J. B.
Burley, Glenn

DOI
10.1002/anie.202313063
URN
urn:nbn:de:101:1-2023111414170616653944
Rechteinformation
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Letzte Aktualisierung
14.08.2025, 10:52 MESZ

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Beteiligte

  • Peschke, Frederik
  • Taladriz‐Sender, Andrea
  • Andrews, Matthew J.
  • Watson, Allan J. B.
  • Burley, Glenn

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