Robb J S, Roy D J, Ghazal P, Allan J, Petrik J
Alba Bioscience, University of Edinburgh, Edinburgh, UK.
Transfus Med. 2006 Apr;16(2):119-29. doi: 10.1111/j.1365-3148.2005.00628.x.
Microarray technology provides an opportunity to monitor multiple parameters simultaneously. High-throughput applications such as blood donation screening could greatly benefit from performing various tests on a single testing platform. Blood grouping represents one part of the donation testing complementing the screening for blood-borne pathogens. Blood group serology traditionally exploited agglutination as the detection method. In this investigation, we have adapted blood grouping reactions to a solid-phase microarray substrate in a non-agglutination reaction format as an initial step in the development of a combined microarray testing platform. We have investigated immobilization of proprietary antibodies on multiple surfaces and monitored their performance under various reaction conditions. For the first time, highly specific blood grouping has been achieved on a planar microarray using directly labelled erythrocytes or a secondary labelled reagent using fluorescent signal end point readout. We have also complemented microarray data with a label-free, surface plasmon resonance-based Biacore platform data and used the real time quantitative measurement to rank anti-A antibodies according to the strength of reaction with the immobilized synthetic blood group antigen A.
微阵列技术提供了同时监测多个参数的机会。诸如献血筛查等高通量应用可以从在单个检测平台上进行各种检测中大大受益。血型鉴定是献血检测的一部分,可补充对血源性病原体的筛查。传统上,血型血清学利用凝集作为检测方法。在本研究中,我们已将血型反应调整为以非凝集反应形式在固相微阵列基质上进行,作为开发联合微阵列检测平台的第一步。我们研究了专有抗体在多个表面上的固定,并监测了它们在各种反应条件下的性能。首次在平面微阵列上使用直接标记的红细胞或使用荧光信号终点读数的二级标记试剂实现了高度特异性的血型鉴定。我们还用基于表面等离子体共振的无标记Biacore平台数据补充了微阵列数据,并使用实时定量测量根据与固定化合成血型抗原A的反应强度对抗A抗体进行排名。