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Monoclonal antibodies raised against 167-180 aa sequence of human carbonic anhydrase XII inhibit its enzymatic activity
- 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.
- Subjects :
- animal structures
Immunoconjugates
medicine.drug_class
Molecular Sequence Data
Gene Expression
Enzyme-Linked Immunosorbent Assay
Biology
Monoclonal antibody
medicine.disease_cause
Epitope
law.invention
Epitopes
Mice
law
Drug Discovery
medicine
Escherichia coli
Animals
Humans
cardiovascular diseases
Amino Acid Sequence
Carbonic Anhydrase Inhibitors
Peptide sequence
Carbonic Anhydrases
Pharmacology
chemistry.chemical_classification
Oligopeptide
Mice, Inbred BALB C
Hybridomas
Antibodies, Monoclonal
Computational Biology
General Medicine
Molecular biology
Transmembrane protein
Recombinant Proteins
Protein Structure, Tertiary
Enzyme
chemistry
Biochemistry
Hemocyanins
Recombinant DNA
Female
Immunization
Oligopeptides
circulatory and respiratory physiology
Subjects
Details
- ISSN :
- 14756374
- Volume :
- 29
- Issue :
- 6
- Database :
- OpenAIRE
- Journal :
- Journal of enzyme inhibition and medicinal chemistry
- Accession number :
- edsair.doi.dedup.....41d4c30bd175709428f99926ad1e67e7