期刊
MOLECULAR PHARMACEUTICS
卷 9, 期 4, 页码 791-802出版社
AMER CHEMICAL SOC
DOI: 10.1021/mp200566k
关键词
electrostatic surface potential; membrane confined electrophoresis; protein charge; viscosity/rheology; second virial coefficient (B-22); interaction parameter (k(D)); static structure factor (S-(q)); hydrodynamic interaction parameter (H-(q)); high concentration monoclonal antibody solution
The present work investigates the influence of electrostatic surface potential distribution of monoclonal antibodies (MAbs) on intermolecular interactions and viscosity. Electrostatic models suggest MAb-1 has a less uniform surface charge distribution than MAb-2. The patches of positive and negative potential on MAb-1 are predicted to favor intermolecular attraction, even in the presence of a small net positive charge. Consistent with this expectation, MAb-1 exhibits a negative second virial coefficient (B-22), an increase in static structure factor,S-(q -> 0), and a decrease in hydrodynamic interaction parameter, H-(q -> 0), with increase in MAb-1 concentration. Conversely, MAb-2 did not show such heterogeneous charge distribution as MAb-1 and hence favors intermolecular repulsion (positive B-22), lower static structure factor, S-(q -> 0), and repulsion induced increase in momentum transfer, H-(q -> 0), to result in lower viscosity of MAb-2. Charge swap mutants of MAb-1, M-5 and M-7, showed a decrease in charge asymmetry and concomitantly a loss in self-associating behavior and lower viscosity than MAb-1. However, replacement of charge residues in the sequence of MAb-2, M-10, did not invoke charge distribution to the same extent as MAb-1 and hence exhibited a similar viscosity and self-association profile as MAb-2.
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