| Literature DB >> 31482666 |
Elizabeth M Santos1,2, Tetyana Berbasova1, Wenjing Wang1, Rahele Esmatpour Salmani1, Wei Sheng1, Chrysoula Vasileiou1, James H Geiger1, Babak Borhan1.
Abstract
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.Entities:
Keywords: hCRBPII; imaging; merocyanine; protein engineering; red fluorescence
Year: 2019 PMID: 31482666 PMCID: PMC7379159 DOI: 10.1002/cbic.201900428
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164