Rosenzweig Z, Yeung E S
Ames Laboratory-USDOE, Iowa State University 50011.
Anal Chem. 1994 May 15;66(10):1771-6. doi: 10.1021/ac00082a028.
A particle-counting immunoassay system for ultrasensitive analysis of proteins in a capillary environment has been developed. The assay is based on the agglutination of antibody-coated particles in the presence of an antigen (usually a protein). The particles were electrophoretically migrated in a 20-microns-i.d. capillary past a detection window where a laser beam irradiates continuously. The light scattering events generated by the agglutinated particles were counted while those produced by unreacted particles were electronically rejected. Glucose-6-phosphate dehydrogenase (G6PDH) was chosen as a test compound for the off-column as well as for the on-column versions of this method. A limit of detection of 620 molecules of G6PDH (1 zmol) was found in the on-column assay. The standard deviation between runs was approximately 6%, which is comparable to that of standard immunoassay methods. The application to the determination of G6PDH levels in individual human erythrocytes is presented. A 14-fold cell-to-cell variation was found which can be explained by the age distribution in the red blood cells.
已开发出一种用于在毛细管环境中对蛋白质进行超灵敏分析的粒子计数免疫分析系统。该分析基于在抗原(通常是蛋白质)存在下抗体包被粒子的凝集。粒子在内径为20微米的毛细管中进行电泳迁移,经过一个检测窗口,激光束在该窗口持续照射。对凝集粒子产生的光散射事件进行计数,同时通过电子方式排除未反应粒子产生的光散射事件。葡萄糖-6-磷酸脱氢酶(G6PDH)被选作该方法柱外和柱上版本的测试化合物。在柱上分析中发现G6PDH的检测限为620个分子(1 zmol)。各次运行之间的标准偏差约为6%,这与标准免疫分析方法相当。介绍了该方法在测定个体人类红细胞中G6PDH水平方面的应用。发现细胞间存在14倍的差异,这可以通过红细胞的年龄分布来解释。