Karanikas V, Patton K, Jamieson G, Pietersz G, McKenzie I
Immunology and Vaccine Laboratory, Austin Research Institute, Heidelberg, Vic., Australia.
Tumour Biol. 1998;19 Suppl 1:71-8. doi: 10.1159/000056507.
The binding affinity of a monoclonal antibody to its ligand has been often used as a qualitative and quantitative measure for the specificity of the antibody. The aim of this paper was to assess the affinity of binding to recombinant and synthetic MUC1 peptides of 52 monoclonal antibodies as part of the ISOBM TD-4 Workshop. Affinity of binding was assessed using a surface plasmon resonance biosensor (BIAcore). The monoclonal antibodies exhibited variable affinity to MUC1 peptides, and overall 25/52 antibodies showed significant binding to the test peptides with affinities ranging from 2.4 x 10(6) to 3.1 x 10(8) M-1. Affinities calculated by analysis of kinetic biosensor data agreed well with affinities determined by equilibrium binding analysis of radiolabelled antibodies. The affinity measurements may provide help when determining the use of various monoclonals in tumour biology research.
单克隆抗体与其配体的结合亲和力常被用作衡量抗体特异性的定性和定量指标。作为国际单克隆抗体标准物委员会(ISOBM)TD-4研讨会的一部分,本文旨在评估52种单克隆抗体与重组及合成MUC1肽段的结合亲和力。使用表面等离子体共振生物传感器(BIAcore)评估结合亲和力。单克隆抗体对MUC1肽段表现出不同的亲和力,总体上25/52种抗体与测试肽段有显著结合,亲和力范围为2.4×10⁶至3.1×10⁸ M⁻¹。通过动力学生物传感器数据分析计算出的亲和力与通过放射性标记抗体的平衡结合分析确定的亲和力吻合良好。亲和力测量在确定各种单克隆抗体在肿瘤生物学研究中的用途时可能会有所帮助。