The development of novel protein-targeted MRI contrast agents crucially depends on the ability to derivatise suitable targeting moieties with a high payload of relaxation enhancer (e.g., gadolinium(III) complexes such as Gd-DOTA), without losing affinity for the target proteins. Here, we report robust synthetic procedures for the preparation of trivalent Gd-DOTA reagents with various chemical handles for site-specific modification of biomolecules. The reagents were shown to successfully label proteins through isothiocyanate ligation or through site-specific thiol-maleimide ligation and strain-promoted azide-alkyne cycloaddition.
CITATION STYLE
Fisher, M. J., Williamson, D. J., Burslem, G. M., Plante, J. P., Manfield, I. W., Tiede, C., … Bon, R. S. (2015). Trivalent Gd-DOTA reagents for modification of proteins. RSC Advances, 5(116), 96194–96200. https://doi.org/10.1039/c5ra20359g
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