Detailed Analytical Characterization of a Bispecific IgG1 CrossMab Antibody of the Knob-into-Hole Format Applying Various Stress Conditions Revealed Pronounced Stability

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 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]
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.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
PDF的下载单位、IP信息已删除 (2025-6-4)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
枫叶应助beizi采纳,获得10
刚刚
1秒前
李健应助高会和采纳,获得10
1秒前
kui完成签到,获得积分10
1秒前
llyyz应助小马采纳,获得20
1秒前
小薇发布了新的文献求助10
2秒前
3秒前
sc发布了新的文献求助10
4秒前
小铭完成签到,获得积分10
4秒前
沐风发布了新的文献求助10
4秒前
希望天下0贩的0应助na采纳,获得10
6秒前
清和发布了新的文献求助10
7秒前
orixero应助玩命的谷槐采纳,获得10
8秒前
9秒前
Owen应助满意的妙海采纳,获得10
9秒前
思源应助顺利亦旋采纳,获得10
11秒前
12秒前
王琦发布了新的文献求助10
12秒前
小马完成签到 ,获得积分10
13秒前
13秒前
herococa应助超帅路灯采纳,获得10
14秒前
14秒前
机智薯片完成签到,获得积分10
14秒前
mumu完成签到,获得积分20
14秒前
Ameko809应助什么李采纳,获得10
15秒前
王树茂完成签到,获得积分10
16秒前
所所应助湛湛采纳,获得10
16秒前
16秒前
17秒前
司空豁应助光亮不平采纳,获得10
18秒前
玩命的谷槐完成签到,获得积分10
18秒前
瞬间完成签到 ,获得积分10
19秒前
小蘑菇应助语默采纳,获得10
20秒前
pcb完成签到,获得积分10
20秒前
21秒前
田様应助xiaoxiao123采纳,获得10
21秒前
Yichen完成签到,获得积分10
22秒前
打打应助mariawang采纳,获得10
23秒前
刘桑桑发布了新的文献求助10
23秒前
奋斗忆灵发布了新的文献求助10
24秒前
高分求助中
The Mother of All Tableaux Order, Equivalence, and Geometry in the Large-scale Structure of Optimality Theory 1370
生物降解型栓塞微球市场(按产品类型、应用和最终用户)- 2030 年全球预测 1000
Implantable Technologies 500
Ecological and Human Health Impacts of Contaminated Food and Environments 400
Phylogenetic study of the order Polydesmida (Myriapoda: Diplopoda) 360
International Relations at LSE: A History of 75 Years 308
Conceptual Metaphor Theory in World Language Education 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 计算机科学 内科学 纳米技术 复合材料 化学工程 遗传学 催化作用 物理化学 基因 冶金 量子力学 免疫学
热门帖子
关注 科研通微信公众号,转发送积分 3926588
求助须知:如何正确求助?哪些是违规求助? 3471199
关于积分的说明 10967396
捐赠科研通 3201047
什么是DOI,文献DOI怎么找? 1768557
邀请新用户注册赠送积分活动 857521
科研通“疑难数据库(出版商)”最低求助积分说明 796061