protein aggregation;
stainless steel;
monoclonal antibody;
kinetics;
mechanism;
adsorption;
INTERLEUKIN-1 RECEPTOR ANTAGONIST;
METHIONINE OXIDATION;
PROTEIN OXIDATION;
STABILITY;
CHALLENGES;
RESIDUES;
D O I:
10.1002/bit.22525
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 [微生物学];
090105 [作物生产系统与生态工程];
摘要:
Stainless steel is a ubiquitous surface in therapeutic protein production equipment and is also present as the needle in pre-filled syringe biopharmaceutical products. Stainless steel microparticles can cause the aggregation of a monoclonal antibody (mAb). The initial rate of mAb aggregation was second order in steel surface area and zero order in mAb concentration, generally consistent with a bimolecular surface aggregation being the rate-limiting step. Polysorbate 20 (PS20) suppressed the aggregation yet was unable to desorb the firmly bound first layer of protein that adsorbs to the stainless steel surface. Also, there was no exchange of mAb from the first adsorbed layer to the bulk phase, suggesting that the aggregation process actually Occurs on subsequent adsorption layers. No oxidized Met residues were detected in the mass spectrum of a digest of a highly aggregated mAb, although there was a fourfold increase in carbonyl groups due to protein oxidation. Biotechnol. Bioeng. 2010;105: 121-129. (C) 2009 Wiley Periodicals, Inc.