Reinecke M, Scheper T
Institut für Technische Chemie, Universität Hannover, Germany.
J Biotechnol. 1997 Dec 17;59(1-2):145-53. doi: 10.1016/s0168-1656(97)00177-6.
An automated immunoassay, with one affinity component immobilized on a solid surface, has been developed to monitor the production of different immunoglobulins during mammalian cell cultivation processes. The whole analysis device is based on the principle of flow injection analysis (FIA) and a cartridge with the immobilized affinity component is implemented into the FIA system. This cartridge is filled with a carrier material to which protein G is covalently bound. After sample injection, binding of the IgG on the protein G within the cartridge takes place while after a washing step, the IgGs are eluted by a pH shift, and the IgG concentration is monitored via fluorescence. In the automated immunoassay, undiluted cell free samples from the reactor or from down-stream processing can be analyzed directly. Due to the separation the IgG can be detected without interference from other sample components by protein fluorescence. The results are obtained with analysis times below 6 min. Sample volumes of less than 100 microliters may be used. The assay is sensitive to concentrations from 5 up to 500 micrograms ml-1. Using this FIA-System, immunoglobulins G, produced in different media, were successfully monitored. The results of the assay were validated by ELISA.
一种自动免疫分析方法已被开发出来,该方法将一种亲和成分固定在固体表面,用于监测哺乳动物细胞培养过程中不同免疫球蛋白的产生。整个分析装置基于流动注射分析(FIA)原理,一个装有固定化亲和成分的试剂盒被应用于FIA系统。该试剂盒填充有一种与蛋白G共价结合的载体材料。进样后,样品中的IgG与试剂盒内的蛋白G结合,经过洗涤步骤后,通过改变pH值洗脱IgG,并通过荧光监测IgG浓度。在自动免疫分析中,可直接分析来自反应器或下游处理的未稀释无细胞样品。由于这种分离方式,通过蛋白质荧光检测IgG时不会受到其他样品成分的干扰。分析时间不到6分钟即可获得结果。可使用体积小于100微升的样品。该检测方法对浓度为5至500微克/毫升的物质敏感。使用这种FIA系统,成功监测了在不同培养基中产生的免疫球蛋白G。该检测方法的结果通过酶联免疫吸附测定(ELISA)得到了验证。