去酰胺
化学
抗体
双特异性抗体
表位
异构化
大小排阻色谱法
压力(语言学)
计算生物学
生物物理学
生物化学
单克隆抗体
酶
生物
免疫学
哲学
催化作用
语言学
作者
Ingrid Grunert,Katrin Heinrich,Juliane Ernst,Michael Hingar,Alexandre Briguet,Michael Leiß,Manfred Wuhrer,Dietmar Reusch,Patrick Bulau
出处
期刊:ACS omega
[American Chemical Society]
日期:2022-01-19
卷期号:7 (4): 3671-3679
被引量:11
标识
DOI:10.1021/acsomega.1c06305
摘要
In recent years, a variety of new antibody formats have been developed. One of these formats allows the binding of one type of antibody to two different epitopes. This can for example be achieved by introduction of the "knob-into-hole" format and a combined CrossMab approach. Due to their complexity, these bispecific antibodies are expected to result in an enhanced variety of different degradation products. Reports on the stability of these molecules are still largely lacking. To address this, a panel of stress conditions, including elevated temperature, pH, oxidizing agents, and forced glycation via glucose incubation, to identify and functionally evaluate critical quality attributes in the complementary-determining and conserved regions of a bispecific antibody was applied in this study. The exertion of various stress conditions combined with an assessment by size exclusion chromatography, ion exchange chromatography, LC-MS/MS peptide mapping, and functional evaluation by cell-based assays was adequate to identify chemical modification sites and assess the stability and integrity, as well as the functionality of a bispecific antibody. Stress conditions induced size variants and post-translational modifications, such as isomerization, deamidation, and oxidation, albeit to a modest extent. Of note, all the observed stress conditions largely maintained functionality. In summary, this study revealed the pronounced stability of IgG1 "knob-into-hole" bispecific CrossMab antibodies compared to already marketed antibody products.
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