Willumsen B, Christian G D, Ruzicka J
Department of Chemistry, University of Washington, Seattle 98195, USA.
Anal Chem. 1997 Sep 1;69(17):3482-9. doi: 10.1021/ac970268h.
An automated system for performing rapid immunoassay, kinetic measurements, and affinity ranking of biomolecular interactions using fluorescence-labeled ligands is described. Its distinctive feature is the automated renewal of solid phase for each measurement, which avoids the need for regeneration of the sensing surface. This system--flow injection renewable surface immunoassay (FIRSI)--is used for the first time here for determination of rate constants for an antibody/antigen interaction and for affinity ranking of several related antigens against one antibody. The performance of the system is compared with a commercial BIAcore system that uses surface plasmon resonance for monitoring biomolecular interactions. While the values of association and dissociation rate constants for human serum albumin (HSA) with monoclonal anti-HSA antibody obtained by these techniques were comparable, it is shown that the FIRSI techniques requires simpler instrumentation, handles a broader size range of analytes, and does not suffer from disturbances caused by changes in the refractive index.
本文描述了一种利用荧光标记配体进行生物分子相互作用的快速免疫测定、动力学测量和亲和力排序的自动化系统。其独特之处在于每次测量时固相的自动更新,这避免了传感表面再生的需要。该系统——流动注射可再生表面免疫测定(FIRSI)——在此首次用于测定抗体/抗原相互作用的速率常数以及几种相关抗原与一种抗体的亲和力排序。将该系统的性能与使用表面等离子体共振监测生物分子相互作用的商业BIAcore系统进行了比较。虽然通过这些技术获得的人血清白蛋白(HSA)与单克隆抗HSA抗体的结合和解离速率常数的值相当,但结果表明,FIRSI技术所需的仪器更简单,能处理更广泛尺寸范围的分析物,且不受折射率变化引起的干扰。