Photo-activated affinity-site cross-linking of antibodies using tryptophan containing peptides
Mike Russ1, Dingyuan Lou, Heinz Kohler
1InNexus Biotechnology, ImmPheron Laboratories, Inc. UK Coldstream Research Campus, 1501 Bull Lea Road, Suite 105, Lexington, KY 40511, USA.
Abstract:
Affinity-based conjugation methods for antibodies can produce defined and reproducible conjugates. This requires that the target antibody has an affinity site for the ligand and that the ligand has a reactive site. These requirements are critical for the conjugation of antibodies designed for diagnostic and therapeutic application. Our laboratory has discovered a novel affinity of antibodies for the amino acid tryptophan using an azido derivative of tryptophan. Here we show that tryptophan without the azido group can be photo-cross-linked to antibodies. Biotinylated tryptophan peptides are photolysed into monoclonal and polyclonal antibodies and such biotinylated antibodies are used in avidin-based ELISA. With the simple and gentle tryptophan-affinity photo-conjugation of peptides, antibodies can be conjugated with peptides to enhance their potency and expand their targeting range.


