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基于膜的分析中酶激活的1,2-二氧杂环丁烷化学发光的增强。

Enhancement of enzyme-activated 1,2-dioxetane chemiluminescence in membrane-based assays.

作者信息

Kobos R K, Blue B A, Robertson C W, Kielhorn L A

机构信息

Corporate New Business Development Division, DuPont Company, Incorporated, Wilmington, Delaware 19880.

出版信息

Anal Biochem. 1995 Jan 1;224(1):128-33. doi: 10.1006/abio.1995.1017.

Abstract

Processes for enhancing the chemiluminescent signal generated by enzyme-activated 1,2-dioxetanes have been developed for membrane-based assays in which detection is done using a charge-coupled device (CCD) camera or X-ray film. The enhancement is demonstrated using slot-blots of biotinylated lambda DNA in conjunction with an avidin-alkaline phosphatase conjugate. For detection with a CCD camera, the nylon membrane is dried after processing and incubation in dioxetane substrate solution and heated to temperatures of 50 to 80 degrees C during detection. Up to a 100-fold signal increase is obtained using this enhancement process compared to the conventional detection procedure, in which the blot is kept saturated with substrate solution in a sealed plastic bag during detection. For detection with X-ray film, a fivefold increase in signal intensity is realized by drying the membrane before exposure to the film. These enhancement processes greatly reduce the time required for detection in membrane-based assays.

摘要

已开发出增强酶激活的1,2 - 二氧杂环丁烷产生的化学发光信号的方法,用于基于膜的检测,其中使用电荷耦合器件(CCD)相机或X射线胶片进行检测。使用生物素化的λDNA的狭缝印迹结合抗生物素蛋白 - 碱性磷酸酶缀合物来证明这种增强效果。对于用CCD相机进行检测,尼龙膜在二氧杂环丁烷底物溶液中处理和孵育后干燥,并在检测期间加热至50至80摄氏度。与传统检测程序相比,使用这种增强方法可使信号增加高达100倍,在传统检测程序中,印迹在检测期间在密封塑料袋中保持被底物溶液饱和。对于用X射线胶片进行检测,通过在膜暴露于胶片之前干燥膜,可使信号强度提高五倍。这些增强方法大大减少了基于膜的检测所需的时间。

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