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Monoclonal antibodies raised against 167-180 aa sequence of human carbonic anhydrase XII inhibit its enzymatic activity

Authors :
Zivile Gudleviciene
Vilma Petrikaite
Visvaldas Kairys
Jurgita Matuliene
Claudiu T. Supuran
Dovile Dekaminaviciute
Milda Zilnyte
Daniela Vullo
Vaida Jogaite
Aurelija Zvirbliene
Source :
Journal of enzyme inhibition and medicinal chemistry. 29(6)
Publication Year :
2014

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.

Details

ISSN :
14756374
Volume :
29
Issue :
6
Database :
OpenAIRE
Journal :
Journal of enzyme inhibition and medicinal chemistry
Accession number :
edsair.doi.dedup.....41d4c30bd175709428f99926ad1e67e7