Engineering of a Red Fluorogenic Protein/Merocyanine Complex for Live-Cell Imaging.
Elizabeth M SantosTetyana BerbasovaWenjing WangRahele Esmatpour SalmaniWei ShengChrysoula VasileiouJames H GeigerBabak BorhanPublished 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.
Keyphrases
- binding protein
- living cells
- quantum dots
- fluorescent probe
- amino acid
- label free
- induced apoptosis
- endothelial cells
- single molecule
- high resolution
- papillary thyroid
- oxidative stress
- energy transfer
- molecular dynamics
- genome wide
- squamous cell carcinoma
- dna methylation
- signaling pathway
- endoplasmic reticulum stress
- transcription factor
- fluorescence imaging
- human immunodeficiency virus
- men who have sex with men
- small molecule
- hiv testing