posted on 2015-02-18, 00:00authored byAnnika Borrmann, Olumide Fatunsin, Jan Dommerholt, Anika M. Jonker, Dennis W. P. M. Löwik, Jan C. M. van Hest, Floris L. van Delft
A main challenge in the area of bioconjugation
is to devise reactions
that are both activatable and fast. Here, we introduce a temporally
controlled reaction between cyclooctynes and 1,2-quinones, induced
by facile oxidation of 1,2-catechols. This so-called strain-promoted
oxidation-controlled cyclooctyne–1,2-quinone cycloaddition
(SPOCQ) shows a remarkably high reaction rate when performed with
bicyclononyne (BCN), outcompeting the well-known cycloaddition of
azides and BCN by 3 orders of magnitude, thereby allowing a new level
of orthogonality in protein conjugation.