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Generation of Recombinant Antibodies against the beta-(1,6)-Branched beta-(1,3)-D-Glucan Schizophyllan from Immunized Mice via Phage Display

Affiliation/Institute
Department for Biotechnology, Institute of Biochemistry, Biotechnology and Bioinformatics
Josewski, Jörn;
Affiliation/Institute
Institute for Physical and Theoretical Chemistry
Buchmeier, Sabine;
GND
131650777
Affiliation/Institute
Department for Biotechnology, Institute of Biochemistry, Biotechnology and Bioinformatics
Frenzel, André;
GND
1069690481
Affiliation/Institute
Institute for Physical and Theoretical Chemistry
Tinnefeld, Philip;
GND
111685311
Affiliation/Institute
Department for Biotechnology, Institute of Biochemistry, Biotechnology and Bioinformatics
Dübel, Stefan;
Affiliation/Institute
Department for Biotechnology, Institute of Biochemistry, Biotechnology and Bioinformatics
Rau, Udo

beta-(1,6)-Branched beta-(1,3)-D-glucans like schizophyllan from the basidiomycete Schizophyllum commune excite various immunostimulatory effects and have been clinically tested as adjuvants. Some of the glucans are also applicable in food or petrol industry due to their viscosity and temperature stability in aqueous solution. Antibodies against these glucans could be used as tool for analysis of glucan preparations or for further research of its bioactivity. Therefore, an immune phage display library was constructed from mice immunized with schizophyllan. Three recombinant monoclonal antibodies were isolated from this library by affinity selection (panning) on schizophyllan. The half-maximal effective concentration (EC50) values for those antibodies varied between 16.4 ng mL−1 and 21.3 ng mL−1. The clones showed binding specificity not only for schizophyllan but also for other beta-(1,6)-branched beta-(1,3)-D-glucans of similar macromolecular structure. Denaturation of the secondary structure led to a reduced antibody binding, indicating an epitope requiring the correct conformation of the triple helical structure of the glucans.

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