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Engineering of a Red Fluorogenic Protein/Merocyanine Complex for Live-Cell Imaging.

Elizabeth M SantosTetyana BerbasovaWenjing WangRahele Esmatpour SalmaniWei ShengChrysoula VasileiouJames H GeigerBabak Borhan
Published in: Chembiochem : a European journal of chemical biology (2019)
A reengineered human cellular retinol binding protein II (hCRBPII), a 15-kDa protein belonging to the intracellular lipid binding protein (iLBP) family, generates a highly fluorescent red pigment through the covalent linkage of a merocyanine aldehyde to an active site lysine residue. The complex exhibits "turn-on" fluorescence, due to a weakly fluorescent aldehyde that "lights up" with subsequent formation of a strongly fluorescent merocyanine dye within the binding pocket of the protein. Cellular penetration of merocyanine is rapid, and fluorophore maturation is nearly instantaneous. The hCRBPII/merocyanine complex displays high quantum yield, low cytotoxicity, specificity in labeling organelles, and compatibility in both cancer cell lines and yeast cells. The hCRBPII/merocyanine tag is brighter than most common red fluorescent proteins.
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