Use of l-Lysine Fluorescence Derivatives as
Tracers To Enhance the Performance of
Polarization Fluoroimmunoassays. A Study Using
Two Herbicides as Model Antigens
posted on 2002-04-27, 00:00authored byGeorge I. Hatzidakis, Aristidis M. Tsatsakis, Elias K. Krambovitis, Apostolos Spyros, Sergei A. Eremin
Fluorescence polarization immunoassay (FPIA) is a convenient homogeneous assay, the use of which is restricted
in environmental analysis by low sensitivity and matrix
effects. We selected the herbicides 2,4D and 2,4,5T to
synthesize new l-lysine-based fluorescent tracers using
solid-phase chemistry. In addition, three different immunogens of 2,4,5T were prepared for immunization and
antibody production. The new tracers and antibodies were
adapted to FPIA. Tracers with the hapten attached to the
α-aminogroup of l-lysine and fluorescein to the e-amino
group exhibited at least a 5-fold increased sensitivity when
compared to the previously reported ethylenediamine-based tracer (2,4D-EDA-F). The isomeric structure (hapten attached to the e-amino and fluorescein to the a-amino
group) appeared 7.6 times less sensitive, and all other
alternative structures exhibited even lower sensitivities.
This observation was confirmed against the monoclonal
anti-2,4D antibody E2/G2 and polyclonal anti-2,4,5T
antibodies. The affinity constant of 2,4D-EDA-F with E2/G2 was 8.1 times higher when compared with the new
tracer, suggesting the more specific nature of the l-lysine-based tracer, the use of which leads to a more sensitive
assay. This type of tracer could improve performance and
lower substantially the detection limits of FPIAs.