Silzel J W, Cercek B, Dodson C, Tsay T, Obremski R J
Beckman Coulter, Inc., Brea, CA 92822-8000, USA.
Clin Chem. 1998 Sep;44(9):2036-43.
Miniaturization of ligand binding assays may reduce costs by decreasing reagent consumption, but it is less apparent that miniaturized assays can simultaneously exceed the sensitivity of macroscopic techniques by analyte "harvesting" to exploit the total analyte mass available in a sample. Capture reagents (avidin or antibodies) immobilized in 200-microm diameter zones are shown to substantially deplete analyte from a liquid sample during a 1-3-h incubation, and the assays that result sense the total analyte mass in a sample rather than its concentration. Detection of as few as 10(5) molecules of analyte per zone is possible by fluorescence imaging in situ on the solid phase using a near-infrared dye label. Single and multianalyte mass-sensing sandwich array assays of the IgG subclasses show the sensitivity and specificity of ELISA methods but use less than 1/100 the capture antibody required by the 96-well plate format.
配体结合分析的小型化可通过减少试剂消耗来降低成本,但小型化分析能通过对分析物的“捕获”同时超过宏观技术的灵敏度,以利用样品中可用的总分析物质量,这一点并不那么明显。固定在直径200微米区域的捕获试剂(抗生物素蛋白或抗体)在1 - 3小时的孵育过程中能从液体样品中大量耗尽分析物,由此产生的分析方法检测的是样品中的总分析物质量而非其浓度。通过使用近红外染料标记在固相上进行原位荧光成像,每个区域检测低至10⁵个分析物分子是可能的。IgG亚类的单分析物和多分析物质量传感夹心阵列分析显示出酶联免疫吸附测定(ELISA)方法的灵敏度和特异性,但所需的捕获抗体不到96孔板形式的1/100。