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Published on: March 25, 2014
Identification of human MHC class I binding peptides using the iTOPIA- epitope discovery system
Markus Wulf1, Petra Hoehn, Peter Trinder
1Thymed GmbH, Mikroforum Ring 2, 55234 Wendelsheim, Germany.
Methods in Molecular Biology (Clifton, N.J.)
|April 21, 2009
Summary
Identifying effective vaccine targets requires precise epitope identification. The iTOPIA assay quickly and easily confirms real-binding to MHC class I molecules, improving epitope screening for cellular immunity.
Area of Science:
- Immunology
- Vaccinology
Background:
- CD8+ T cells are vital for cellular immunity and long-term protection against infectious diseases.
- Identifying relevant antigens and epitopes is crucial for developing effective vaccines.
- Current methods for defining MHC class I-binding epitopes are often time-consuming and require limited biological material.
Purpose of the Study:
- To introduce and validate the iTOPIA assay for determining real-binding to MHC class I molecules.
- To provide a rapid and efficient platform for screening and identifying potential T cell epitopes.
Main Methods:
- The iTOPIA assay was developed to assess the binding of peptides to MHC class I molecules.
- The assay's performance was evaluated for its speed, ease of use, and accuracy in identifying binding epitopes.
Main Results:
- The iTOPIA assay is a quick and easy-to-perform method for determining real-binding to MHC class I.
- It offers an excellent platform for screening and eliminating potential epitopes.
- The assay facilitates the identification of novel epitopes prior to functional assay validation.
Conclusions:
- The iTOPIA assay significantly improves the process of epitope identification for vaccine development.
- It offers a valuable tool for researchers seeking to enhance cellular immunity through targeted epitope selection.

