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一种使用光固定微阵列的自动化多重特异性 IgE 检测系统。

An automated multiplex specific IgE assay system using a photoimmobilized microarray.

机构信息

Nano Medical Engineering Laboratory, RIKEN Advanced Science Institute, 2-1 Hirosawa, Wako-shi, Saitama, 351-0198, Japan.

出版信息

J Biotechnol. 2012 Nov 15;161(4):414-21. doi: 10.1016/j.jbiotec.2012.07.196. Epub 2012 Aug 16.

Abstract

An automated microarray diagnostic system for specific IgE using photoimmobilized allergen has been developed. Photoimmobilization is useful for preparing microarrays, where various types of biological components are covalently immobilized on a plate. Because the immobilization is based on a photo-induced radical cross-linking reaction, it does not require specific functional groups on the immobilized components. Here, an aqueous solution of a photoreactive poly(ethylene glycol)-based polymer was spin-coated on a plate, and an aqueous solution of each allergen was microspotted on the coated plate and allowed to dry in air. Finally, the plate was irradiated with an ultraviolet lamp for covalent immobilization. An automated machine using these plates was developed for the assay of antigen-specific IgE. Initially, the patient serum was added to the microarray plate, and after reaction of the microspotted allergen with IgE, the adsorbed IgE was detected by a peroxidase-conjugated anti-IgE-antibody. The chemical luminescence intensity of the substrate decomposed by the peroxidase was automatically detected using a sensitive charge-coupled device camera. All the allergens were immobilized stably using this method, which was used to screen for allergen-specific IgE. The results were comparable with those using conventional specific IgE. Using this system, six different allergen-specific IgE were assayed using 10 μL of serum within a period of 20 min.

摘要

已经开发出一种使用光固定过敏原的特定 IgE 的自动化微阵列诊断系统。光固定对于制备微阵列非常有用,其中各种类型的生物成分通过共价键固定在板上。由于固定基于光诱导的自由基交联反应,因此不需要固定成分上的特定功能基团。在这里,将光反应性基于聚乙二醇的聚合物的水性溶液旋涂在板上,并将每种过敏原的水性溶液微点样在涂覆的板上,并在空气中干燥。最后,用紫外线灯照射以进行共价固定。开发了一种使用这些板的自动化机器来测定抗原特异性 IgE。最初,将患者血清添加到微阵列板中,并且在微点样的过敏原与 IgE 反应之后,通过过氧化物酶缀合的抗 IgE 抗体检测吸附的 IgE。通过灵敏的电荷耦合器件 (CCD) 相机自动检测过氧化物酶分解的底物的化学发光强度。使用这种方法稳定地固定了所有过敏原,并用其来筛选过敏原特异性 IgE。结果与常规特异性 IgE 相当。使用该系统,在 20 分钟的时间内使用 10 μL 血清测定了六种不同的过敏原特异性 IgE。

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