A fluorescence binding assay was developed for a small peptide based on a f
usion protein between the peptide and the green fluorescent protein, GFP. T
he assay employs genetic engineering methods to prepare the analyte-label (
peptide-GFP) conjugate as a fusion protein in order to produce a one-to-one
, homogenous population of labeled-peptide. Specifically, a plasmid was con
structed in which the C-terminus of a model octapeptide was fused to the N-
terminus of GFP. Following expression of the octapeptide-GFP fusion protein
in Escherichia coli, an immunoassay was developed based on sequential bind
ing of the free octapeptide and labeled-octapeptide to an anti-octapeptide
antibody immobilized on a solid surface. The naturally fluorescent protein
acts as a label to provide sensitive detection for peptides. To our knowled
ge, this is the first time that GFP has been used as a quantitative label i
n a fusion protein to develop a quantitative assay for a peptide analyte. (
C) 1999 Elsevier Science B.V. All rights reserved.