Abstract
Azobenzenes have been used as photoresponsive units for the control of numerous biological processes. Primary prerequisites for such applications are site-selective incorporation of photoswitchable units into biomolecules and the possibility of using non-destructive and deep-tissue-penetrating visible light for the photoisomerization. Here we report a push-pull azobenzene that readily undergoes a Staudinger-Bertozzi ligation with azide groups, that can be addressed with visible light (>440 nm) and exhibits the solvato- and acidochromism typical for push-pull systems. The thermal relaxation in aqueous environment proceeds on the low-millisecond timescale, thus enabling control over biological processes on similar timescales. The approach is demonstrated in the modification of a quartz surface and in the incorporation of an azobenzene unit into a functional peptide, the third zinc finger in the mammalian factor Sp1. Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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Poloni, C., Szymański, W., Hou, L., Browne, W. R., & Feringa, B. L. (2014). A fast, visible-light-sensitive azobenzene for bioorthogonal ligation. Chemistry - A European Journal, 20(4), 946–951. https://doi.org/10.1002/chem.201304129
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