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Development of a new parallelized, optical biosensor platform for label-free detection of autoimmunity-related antibodies

机译:新型平行光学生物传感器平台的开发,可无标记地检测自身免疫相关抗体

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摘要

Autoimmune diseases are characterized by the presence of autoantibodies in serum of affected patients. The heterogeneity of autoimmune relevant antigens creates a variety of different antibodies, which requires a simultaneous detection mode. For this reason, we developed a tool for parallelized, label-free, optical detection that accomplishes the characterization of multiple antigen-antibody interactions within a single measurement on a timescale of minutes. Using 11-aminoundecyltrimethoxysilane, we were able to immobilize proteinogenic antigens as well as an amino-functionalized cardiolipin on a glass surface. Assay conditions were optimized for serum measurements with a single spot antigen chip on a single spot 1-λ detection system. Minimized background signal allows a differentiation between patients and healthy controls with a good sensitivity and specificity. Applying polarized imaging reflectometric interference spectroscopy, we evaluated samples from three APS patients and three control subjects for this proof-of-principle and already obtained good results for β2-glycoprotein I and cardiolipin.
机译:自身免疫疾病的特征是在受影响患者的血清中存在自身抗体。自身免疫相关抗原的异质性产生了多种不同的抗体,需要同时进行检测。因此,我们开发了一种用于并行,无标记的光学检测的工具,该工具可在几分钟的时间内完成一次测量中多个抗原-抗体相互作用的表征。使用11-氨基十一烷基三甲氧基硅烷,我们能够将蛋白原性抗原以及氨基官能化的心磷脂固定在玻璃表面上。优化了检测条件,用于在单点1-λ检测系统上使用单点抗原芯片进行血清测量。最小化的背景信号允许以良好的敏感性和特异性区分患者和健康对照。应用偏振成像反射干涉光谱法,我们评估了三名APS患者和三名对照受试者的样品的这一原理证明,并且已经获得了β2-糖蛋白I和心磷脂的良好结果。

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