Copper‐Free Click Reactions with Polar Bicyclononyne Derivatives for Modulation of Cellular Imaging |
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Authors: | E. H. P. Leunissen M. H. L. Meuleners Dr. J. M. M. Verkade J. Dommerholt Prof. J. G. J. Hoenderop Dr. F. L. van Delft |
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Affiliation: | 1. Institute for Molecules and Materials, Heyendaalseweg 135, 6525 AJ Nijmegen (The Netherlands);2. Physiology, Radboud University Medical Centre, P.O. Box 9101, 6500 HB Nijmegen (The Netherlands);3. SynAffix B.V. Molenweg 79, 5349 AC Nijmegen (The Netherlands) |
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Abstract: | The ability of cells to incorporate azidosugars metabolically is a useful tool for extracellular glycan labelling. The exposed azide moiety can covalently react with alkynes, such as bicyclo[6.1.0]nonyne (BCN), by strain‐promoted alkyne–azide cycloaddition (SPAAC). However, the use of SPAAC can be hampered by low specificity of the cycloalkyne. In this article we describe the synthesis of more polar BCN derivatives and their properties for selective cellular glycan labelling. The new polar derivatives [amino‐BCN, glutarylamino‐BCN and bis(hydroxymethyl)‐BCN] display reaction rates similar to those of BCN and are less cell‐permeable. The labelling specificity in HEK293 cells is greater than that of BCN, as determined by confocal microscopy and flow cytometry. Interestingly, amino‐BCN appears to be highly specific for the Golgi apparatus. In addition, the polar BCN derivatives label the N‐glycan of the membrane calcium channel TRPV5 in HEK293 cells with significantly enhanced signal‐to‐noise ratios. |
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Keywords: | BCN click chemistry glycosylation HEK293 cells imaging agents SPAAC |
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