Maltare Astha, Nietz Angela K, Laszczyk Ann M, Dunn Taylor S, Ballestas Mary E, Accavitti-Loper Mary Ann, King Gwendalyn D
1 Department of Neurobiology, University of Alabama at Birmingham , Alabama.
Monoclon Antib Immunodiagn Immunother. 2014 Dec;33(6):420-7. doi: 10.1089/mab.2014.0040.
Although antibodies are commercially available to allow investigation into the biology of the age-regulating protein Klotho, problems with antibody specificity and application functionality are significant barriers to progress. Chief among these limitations is the inability of current tools to allow in vivo validation of binding partners originally identified through transfection of tagged proteins. To overcome this barrier, we generated a series of hybridoma cell lines by immunizing rats with a GST-KL1 fusion protein. Purified antibodies generated from these cell lines differentially detect human or mouse Klotho protein via Western blot, immunocyto/histochemistry, and immunoprecipitation. Specificity of antibody binding to Klotho was confirmed by mass spectrometry following immunoprecipitation. With this confidence in antibody specificity, co-immunoprecipitation was utilized to validate the interaction of Klotho/FGFR and Klotho/wnt7a in mouse kidney lysates.
尽管有商业抗体可用于研究衰老调节蛋白α-klotho的生物学特性,但抗体特异性和应用功能方面的问题是研究进展的重大障碍。这些局限性中最主要的是,目前的工具无法对最初通过转染标记蛋白鉴定出的结合伴侣进行体内验证。为克服这一障碍,我们用GST-KL1融合蛋白免疫大鼠,生成了一系列杂交瘤细胞系。从这些细胞系中纯化得到的抗体,可通过蛋白质免疫印迹法、免疫细胞/组织化学法和免疫沉淀法,差异检测人或小鼠的α-klotho蛋白。免疫沉淀后通过质谱法确认了抗体与α-klotho结合的特异性。基于对抗体特异性的这种信心,我们利用免疫共沉淀法在小鼠肾脏裂解物中验证了α-klotho/FGFR和α-klotho/wnt7a的相互作用。