发布: 2013年12月20日第3卷第24期 DOI: 10.21769/BioProtoc.1006 浏览次数: 13148
评审: Anonymous reviewer(s)
相关实验方案
Cell-Sonar:通过特定蛋白标志物表达变化追踪目标蛋白的简便低成本方法
Sabrina Brockmöller [...] Simone Rothmiller
2025年02月05日 770 阅读
Abstract
Molecular interaction between monoclonal antibodies (MAbs) and their recognized antigen is a fundamental event leading to the neutralization activity. Estimation of their binding affinity gives beneficial information to characterize the MAbs and to develop more effective MAbs. Surface plasmon resonance (SPR) analysis is a powerful tool to analyze the molecular interaction, enabling rapid and repetitive estimation with relatively small amount of sample. Here we describe a general protocol about SPR analysis on the interaction between viral antigen and human MAb (HuMAb) IgG. Anti-human Fcγ is first covalently crosslinked on the sensor chip by amine coupling, and then HuMAb of interest is immobilized via anti-Fcγ MAb IgG interaction as ligand. Antigen injected on the sensor chip causes the SPR change in time course as the result of association and dissociation. By analyzing the kinetics, association rate, dissociation rate, and dissociation constant are obtained.
Keywords: Molecular interaction (分子相互作用)Materials and Reagents
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文章信息
版权信息
© 2013 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Readers should cite both the Bio-protocol article and the original research article where this protocol was used:
分类
免疫学 > 抗体分析 > 抗体-抗原相互作用
生物化学 > 蛋白质 > 相互作用
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