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首页> 外文期刊>Analytical and bioanalytical chemistry >A new fluorescence sensor developed with polydopamine nanospheres for the detection of anti-PLA2R antibody biomarkers of idiopathic membranous nephropathy
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A new fluorescence sensor developed with polydopamine nanospheres for the detection of anti-PLA2R antibody biomarkers of idiopathic membranous nephropathy

机译:用多碳胺纳米球开发的新荧光传感器,用于检测特发性膜肾病的抗PLA2R抗体生物标志物

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Anti-PLA2R antibody is only expressed in podocytes from patients with idiopathic membranous nephropathy (IMN). The detection of anti-PLA2R antibody in serum is therefore able to obtain essential information for rapid diagnosis and evaluation of the disease activity of IMN. In the present study, a polydopamine nanosphere-based fluorescent sensor was constructed for direct detection of anti-PLA2R antibodies in human serum. In this sensing system, the double-stranded DNA was phosphorylated under the action of anti-PLA2R antibody and the single-stranded DNA was cut by exonuclease. The single-stranded DNA was then adsorbed on polydopamine microspheres. The fluorescent groups labeled on the DNA were quenched, and the concentration of anti-PLA2R antibody was detected quantitatively by measuring the fluorescence signal changes before and after the reaction. The experimental results show that the method has a good linear detection range between 0.05 and 10 mu g/mL for anti-PLA2R antibody and the detection limit is 0.02 mu g/mL.
机译:抗PLA2R抗体仅以来自特发性膜肾病(IMN)的患者的诱导患者表示。因此,血清中抗PLA2R抗体的检测能够获得快速诊断和评估IMN的疾病活性的基本信息。在本研究中,构建了一种聚二氨基氨基纳米环基荧光传感器,用于直接检测人血清中的抗PLA2R抗体。在该感测系统中,在抗PLA2R抗体的作用下双链DNA磷酸化,通过外切核酸酶切割单链DNA。然后将单链DNA吸附在聚二胺微球上。淬灭在DNA上标记的荧光基团,通过测量反应前后的荧光信号变化来定量检测抗PLA2R抗体的浓度。实验结果表明,该方法具有0.05至10μg/ ml的良好的抗PLA2R抗体的线性检测范围,检测极限为0.02μg/ ml。

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