Journal of Enzyme Inhibition and Medicinal Chemistry · 2014 · 21 citations · 29 references
PharmacyBiochemistryOncologyAntibody EngineeringMolecular OncologyMonoclonal AntibodiesAntibody CharacterizationAntibody DiscoveryAntibody StructureAntibody-antigen RecognitionTherapeutic Antibody DevelopmentTherapeutic Monoclonal AntibodiesAntibodiesAntibody Specificity AnalysisCarbonic Anhydrase InhibitorsCatalytic DomainsMonoclonal Antibodies In CancerMonoclonal Antibodies In OncologyMonoclonal Antibody DesignMonoclonal Antibody Therapeutics
Abstract Human carbonic anhydrase XII (CA XII) is a single-pass transmembrane protein with an extracellular catalytic domain. This enzyme is being recognized as a potential biomarker for different tumours. The current study was aimed to generate monoclonal antibodies (MAbs) neutralizing the enzymatic activity of CA XII. Bioinformatics analysis of CA XII structure revealed surface-exposed sequences located in a proximity of its catalytic centre. Two MAbs against the selected antigenic peptide spanning 167-180 aa sequence of CA XII were generated. The MAbs were reactive with recombinant catalytic domain of CA XII expressed either in E. coli or mammalian cells. Inhibitory activity of the MAbs was demonstrated by a stopped flow CO2 hydration assay. The study provides new data on the surface-exposed linear CA XII epitope that may serve as a target for inhibitory antibodies with a potential immunotherapeutic application.
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Basic local alignment search tool
Stephen F. Altschul, Warren Gish, Webb Miller et al. · Journal of Molecular Biology · 1990 · 94.5K citations
Ahmedin Jemal, Freddie Bray, Jacques Ferlay et al. · CA A Cancer Journal for Clinicians · 2011 · 55K citations · Full text
Continuous cultures of fused cells secreting antibody of predefined specificity
Georges Köhler, César Milstein · Nature · 1975 · 17.2K citations
Pharmacy, Cell Biology, Immunology +11