Matsudaira Takahiro, Tsuzuki Saki, Wada Akira, Suwa Akira, Kohsaka Hitoshi, Tomida Maiko, Ito Yoshihiro
Nano Medical Enginering Laboratory, RIKEN (The Institute of Physical and Chemical Research), Wako, Saitama, Japan.
Biotechnol Prog. 2008 Nov-Dec;24(6):1384-92. doi: 10.1002/btpr.63.
Autoimmune diseases such as rheumatoid arthritis, multiple sclerosis, and autoimmune diabetes are characterized by the production of autoantibodies that serve as useful diagnostic markers, surrogate markers, and prognostic factors. We devised an in vitro system to detect these clinically pivotal autoantibodies using a photoimmobilized autoantigen microarray. Photoimmobilization was useful for preparing the autoantigen microarray, where autoantigens are covalently immobilized on a plate, because it does not require specific functional groups of the autoantigens and any organic material can be immobilized by a radical reaction induced by photoirradiation. Here, we prepared the microarray using a very convenient method. Aqueous solutions of each autoantigen were mixed with a polymer of poly(ethylene glycol) methacrylate and a photoreactive crosslinker, and the mixtures were microspotted on a plate and dried in air. Finally, the plate was irradiated with an ultraviolet lamp to obtain immobilization. In the assay, patient serum was added to the microarray plate. Antigen-specific IgG adsorbed on the microspotted autoantigen was detected by peroxidase-conjugated anti-IgG antibody. The chemical luminescence intensities of the substrate decomposed by the peroxidase were detected with a sensitive CCD camera. All autoantigens were immobilized stably by this method and used to screen antigen-specific IgG. In addition, the plate was covered with a polydimethylsiloxane sheet containing microchannels and automated measurement was carried out.
类风湿性关节炎、多发性硬化症和自身免疫性糖尿病等自身免疫性疾病的特征是产生自身抗体,这些自身抗体可作为有用的诊断标志物、替代标志物和预后因素。我们设计了一种体外系统,使用光固定自身抗原微阵列来检测这些临床上关键的自身抗体。光固定对于制备自身抗原微阵列很有用,在该微阵列中,自身抗原通过共价方式固定在平板上,因为它不需要自身抗原的特定官能团,并且任何有机材料都可以通过光照射诱导的自由基反应进行固定。在这里,我们使用一种非常简便的方法制备了微阵列。将每种自身抗原的水溶液与聚甲基丙烯酸乙二醇酯聚合物和光反应性交联剂混合,然后将混合物微点样到平板上并在空气中干燥。最后,用紫外灯照射平板以实现固定。在检测中,将患者血清加入到微阵列平板中。通过过氧化物酶偶联的抗IgG抗体检测吸附在微点样自身抗原上的抗原特异性IgG。用过氧化物酶分解底物的化学发光强度用灵敏的电荷耦合器件相机进行检测。通过这种方法,所有自身抗原都被稳定固定,并用于筛选抗原特异性IgG。此外,平板上覆盖有包含微通道的聚二甲基硅氧烷片,并进行了自动测量。