Sun Haixiang, Ge Baosheng, Liu Shengnan, Chen Huanlin
College of Chemistry and Chemical Engineering, China University of Petroleum, Dongying, Shandong, PR China.
J Sep Sci. 2008 Apr;31(6-7):1201-6. doi: 10.1002/jssc.200700508.
In this study, recombinant allophycocyanin (rAPC) with a purity of 98% was transferred from a gel to a nitrocellulose (NC) membrane to develop a simple and efficient immuno-affinity membrane. Atomic force microscopy (AFM) was used to investigate the surface topography of the affinity membrane and its characterization indicated that rAPC easily forms trimers or hexamers on the membrane surface on use of the given transfer method. The hydrodynamic radius (R(h)) of the rAPC aggregation was equal to 103 nm or 365 nm according to dynamic light scattering (DLS), which was in agreement with the result obtained by AFM. Based on the specific immunological reaction of antigen and antibody, anti-APC antibodies were purified from rabbit polyclonal serum in a single step. The amount of absorbed antibody was 5.79 mg/g membrane according to analysis by ELISA methods. The purity of antibodies was up to 98% according to SDS-PAGE. The adsorption-desorption cycle of rAPC was repeated six times using the same immuno-affinity membrane, and there was no significant loss in adsorption capacity. The method provides a novel and efficient immunological affinity membrane for the purification of antibodies.
在本研究中,将纯度为98%的重组别藻蓝蛋白(rAPC)从凝胶转移至硝酸纤维素(NC)膜上,以制备一种简单高效的免疫亲和膜。采用原子力显微镜(AFM)研究亲和膜的表面形貌,其表征表明,使用给定的转移方法时,rAPC在膜表面容易形成三聚体或六聚体。根据动态光散射(DLS),rAPC聚集体的流体动力学半径(R(h))等于103 nm或365 nm,这与AFM获得的结果一致。基于抗原与抗体的特异性免疫反应,一步从兔多克隆血清中纯化抗APC抗体。根据ELISA方法分析,抗体吸附量为5.79 mg/g膜。根据SDS-PAGE,抗体纯度高达98%。使用同一免疫亲和膜重复rAPC的吸附-解吸循环6次,吸附容量无显著损失。该方法为抗体纯化提供了一种新型高效的免疫亲和膜。