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21 February 2008 Fluorescence correlation spectroscopy to study antibody binding and stoichiometry of complexes
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Abstract
FCS (fluorescence correlation spectroscopy) was used to study the association at the single molecule level of tumor necrosis factor alpha (TNF-α) and two of its protein antagonists Humira(TM) (adalimumab), a fully humanized monoclonal antibody, and Enbrel(TM) (etanercept), a soluble form of the TNF receptor. Single molecule approaches potentially have the advantage not only of enhanced sensitivity, but also of observing at equilibrium the details that would otherwise be lost in classical ensemble experiments where heterogeneity is averaged. We prepared fluorescent conjugates of the protein drugs and their biological target, the trimeric soluble form of TNF-α. The bivalency of adalimumab and the trimeric nature of TNF-α potentially allow several forms of associative complexes that may differ in stoichiometry. Detailed knowledge of this reaction may be relevant to understanding adalimumab's pharmacological properties. Our FCS data showed that a single trimeric TNF-α can bind up to three adalimumab molecules. Under some conditions even larger complexes are formed, apparently the result of cross-linking of TNF-α trimers by adalimumab. In addition, distinct differences between Humira and Enbrel were observed in their association with TNF-α.
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Kerry M. Swift and Edmund D. Matayoshi "Fluorescence correlation spectroscopy to study antibody binding and stoichiometry of complexes", Proc. SPIE 6862, Single Molecule Spectroscopy and Imaging, 686208 (21 February 2008); https://doi.org/10.1117/12.767807
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