Journal
ANTIBODIES
Volume 10, Issue 1, Pages -Publisher
MDPI
DOI: 10.3390/antib10010011
Keywords
HDX-MS; hydrogen-deuterium exchange; mass spectrometry; proteolysis-resistant protein; ANXA1; annexin-A1; conformational epitope mapping
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Funding
- State Ministry of Baden-Wuerttemberg for Economic Affairs, Labour and Housing Construction
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This study identified the interaction site between an ANXA1-specific antibody and ANXA1 using HDX-MS, revealing the binding region within domain III of ANXA1. The antibody-binding region corresponds to the hydrophobic binding pocket of the N-terminal domain in the absence of calcium. This demonstrates the potential of HDX-MS in studying binding regions and defining action profiles of antibodies for therapy.
Annexin-A1 (ANXA1) belongs to a class of highly homologous Ca2+-dependent phospholipidbinding proteins. Its structure consists of a core region composed of four homologous repeats arranged in a compact, hydrolysis-resistant structure and an N-terminal region with a Ca2+-dependent conformation. ANXA1 is involved in several processes, including cell proliferation, apoptosis, metastasis, and the inflammatory response. Therefore, the development of antibodies blocking selected regions on ANXA1 holds great potential for the development of novel therapeutics treating inflammatory and cancer diseases. Here, we report the interaction site between an ANXA1-specific antibody known to inhibit T cell activation without adverse cytotoxic effects and ANXA1 using amide hydrogen-deuterium exchange mass spectrometry (HDX-MS). For the epitope determination, we applied two bottom-up HDX-MS approaches with pepsin digestion in solution and immobilized on beads. Both strategies revealed the interaction region within domain III of ANXA1 in Ca2+-bound conformation. The antibody-binding region correlates with the hydrophobic binding pocket of the N-terminal domain formed in the absence of calcium. This study demonstrates that even cryptic and flexible binding regions can be studied by HDX-MS, allowing a fast and efficient determination of the binding sites of antibodies which will help to define a mode of action profile for their use in therapy.
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