| Literature DB >> 34121411 |
Alfredo Lanzaro1, Aisling Roche2, Nicole Sibanda2, Daniel Corbett2, Peter Davis3, Maryam Shah4, Jai A Pathak5, Shahid Uddin5, Christopher F van der Walle5, Xue-Feng Yuan1, Alain Pluen4, Robin Curtis2.
Abstract
High-concentration (>100 g/L) solutions of monoclonal antibodies (mAbs) are typically characterized by anomalously large solution viscosity and shear thinning behavior for strain rates ≥103 s-1. Here, the link between protein-protein interactions (PPIs) and the rheology of concentrated solutions of COE-03 and COE-19 mAbs is studied by means of static and dynamic light scattering and microfluidic rheometry. By comparing the experimental data with predictions based on the Baxter sticky hard-sphere model, we surprisingly find a connection between the observed shear thinning and the predicted percolation threshold. The longest shear relaxation time of mAbs was much larger than that of model sticky hard spheres within the same region of the phase diagram, which is attributed to the anisotropy of the mAb PPIs. Our results suggest that not only the strength but also the patchiness of short-range attractive PPIs should be explicitly accounted for by theoretical approaches aimed at predicting the shear rate-dependent viscosity of dense mAb solutions.Entities:
Keywords: bioprocessing; monoclonal antibodies; protein−protein interactions; rheology; shear thinning
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Year: 2021 PMID: 34121411 DOI: 10.1021/acs.molpharmaceut.1c00198
Source DB: PubMed Journal: Mol Pharm ISSN: 1543-8384 Impact factor: 4.939