Hydrogen-deuterium exchange mass spectrometry reveals three unique binding responses of mAbs directed to the catalytic domain of hCAIX. Issue 1 (1st January 2021)

• Record Type: Journal Article
• Authors: Sheff, Joey G.; Kelly, John F.; Robotham, Anna; Sulea, Traian; Malenfant, Félix; L'Abbé, Denis; Duchesne, Mélanie; Pelletier, Alex; Lefebvre, Jean; Acel, Andrea; Parat, Marie; Gosselin, Mylene; Wu, Cunle; Fortin, Yves; Baardsnes, Jason; Van Faassen, Henk; Awrey, Shannon; Chafe, Shawn C.; McDonald, Paul C.; Dedhar, Shoukat; Lenferink, Anne E.G.
• Is Part Of: MAbs. Volume 13:Issue 1(2021)
• Publication Date: 2021-01-01
• Subjects: Carbonic anhydrase -- hydrogen-deuterium exchange -- mass spectrometry -- epitope mapping -- anti-cancer target -- antibody-drug conjugate -- allostery -- antibody -- tumor microenvironment; Monoclonal antibodies -- Therapeutic use -- Periodicals; Monoclonal antibodies -- Periodicals; Antibodies, Monoclonal -- Periodicals; 616.0798
• DOI: 10.1080/19420862.2021.1997072
• Languages: English
• ISSNs: 1942-0862

Abstract

ABSTRACT: Human carbonic anhydrase (hCAIX), an extracellular enzyme that catalyzes the reversible hydration of CO2, is often overexpressed in solid tumors. This enzyme is instrumental in maintaining the survival of cancer cells in a hypoxic and acidic tumor microenvironment. Absent in most normal tissues, hCAIX is a promising therapeutic target for detection and treatment of solid tumors. Screening of a library of anti-hCAIX monoclonal antibodies (mAbs) previously identified three therapeutic candidates (mAb c2C7, m4A2 and m9B6) with distinct biophysical and functional characteristics. Selective binding to the catalytic domain was confirmed by yeast surface display and isothermal calorimetry, and deeper insight into the dynamic binding profiles of these mAbs upon binding were highlighted by bottom-up hydrogen-deuterium exchange mass spectrometry (HDX-MS). Here, a conformational and allosterically silent epitope was identified for the antibody-drug conjugate candidate c2C7. Unique binding profiles are described for both inhibitory antibodies, m4A2 and m9B6. M4A2 reduces the ability of the enzyme to hydrate CO2 by steric gating at the entrance of the catalytic cavity. Conversely, m9B6 disrupts the secondary structure that is necessary for substrate binding and hydration. The synergy of these two inhibitory mechanisms is demonstrated in in vitro activity assays and HDX-MS. Finally, the ability of m4A2 to modulate extracellular pH and intracellular metabolism is reported. By highlighting three unique modes by which hCAIX can be targeted, this study demonstrates both the utility of HDX-MS as an important tool in the characterization of anti-cancer biotherapeutics, and the underlying value of CAIX as a therapeutic target.