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Updated: May 3, 2026

A High Throughput MHC II Binding Assay for Quantitative Analysis of Peptide Epitopes
Published on: March 25, 2014
Competitive Epitope Binning Using HT-SPR.
Daniel Bedinger1, Judicael Parisot2, Noah T Ditto2
1Carterra Inc, Salt Lake City, UT, USA. dbedinger@carterra-bio.com.
High-throughput surface plasmon resonance (HT-SPR) enables competitive epitope binning for hundreds of antibodies. This method analyzes antibody binding profiles and clusters those with shared epitopes for deeper understanding.
Area of Science:
- Biochemistry
- Immunology
- Biotechnology
Background:
- Competitive epitope binning is crucial for characterizing monoclonal antibodies.
- High-throughput surface plasmon resonance (HT-SPR) offers a scalable solution for this analysis.
- Understanding antibody-epitope interactions is vital in drug discovery and development.
Purpose of the Study:
- To detail an approach for competitive epitope binning using the Carterra LSA.
- To provide considerations for the design and analysis of HT-SPR based binning assays.
- To demonstrate the utility of HT-SPR for profiling numerous monoclonal antibodies.
Main Methods:
- Monoclonal antibodies are arrayed on a biosensor chip.
- Serial interrogation assesses trimolecular complex formation with antigen and solution-phase antibodies.
- Carterra LSA software facilitates real-time data analysis and epitope clustering.
Main Results:
- Successful implementation of a competitive epitope binning assay using HT-SPR.
- Clustering of monoclonal antibodies based on shared epitope binding profiles.
- Real-time data acquisition enabled detailed analysis of individual antibody binding characteristics.
Conclusions:
- HT-SPR provides an efficient method for competitive epitope binning of hundreds of antibodies.
- The described approach facilitates the understanding of antibody epitope profiles.
- This technique aids in the characterization and selection of monoclonal antibodies.
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