Measurement intensification for antibody formulations: combined measurement of protein size, interactions, and viscosity by differential dynamic microscopy
Gupit, C. I.; Shandilya, A.; Uruena, J. M.; Morales-Cummings, N.; Gupta, R.; Valentine, M. T.; Helgeson, M. E.
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High-throughput screening and optimization of high-value protein formulations requires intensified measurements to extract a wide range of properties using a small number of measurement techniques, small sample volumes, and short measurement times. We demonstrate how differential dynamic microscopy (DDM) can fill this need by measuring a broad range of key biophysical properties relevant to protein formulations from a single workflow on microliter-scale samples using label-free video optical microscopy. We show that the use of phase contrast imaging dramatically enhances measurement resolution for protein solutions at dilute and semidilute concentrations, enabling measurement of colloidal properties such as protein-protein interactions, protein size, aggregation, and solution viscosity from a single set of measurements. DDM measurements on a representative human immunoglobulin (IgG) system yield estimates for the hydrodynamic radius (Rh), second osmotic virial coefficient (B2), and hydrodynamic interaction (kd) that are consistent with independently measured values, validating the ability of DDM to extract these parameters from a single set of measurements. Observed trends in B2 with pH and ionic strength are consistent with the antibodys charge and screened electrostatics, demonstrating the ability of DDM to provide insight on protein-protein interactions. To show the utility of DDM as a "multitool" for quantifying multiple formulation properties from a single measurement, we use the results to test a predictive colloidal model for the solution viscosity, which is in fair agreement with measurements obtained using DDM-based microrheology. Combined with low sample requirements and short measurement times, DDM thus offers a high-throughput and efficient route to accelerate protein biophysics and formulation development. SIGNIFICANCE STATEMENTThe formulation of stable, high-concentration antibodies and other protein solutions requires extensive biophysical measurements that are often material- and time-intensive. We demonstrate that differential dynamic microscopy (DDM) provides a powerful alternative by providing rapid access to a broad range of industrially relevant colloidal properties from a single measurement on microliter-scale samples using conventional video optical microscopy. This capability makes DDM an attractive, low-resource approach for routine biomolecular formulation screening and optimization.
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