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Detection of multiple proteins on one spot by laser ablation inductively coupled plasma mass spectrometry and application to immuno-microarray with element-tagged antibodies

机译:激光消融电感耦合等离子体质谱法在一处检测多种蛋白质,并将其应用于带有元素标签抗体的免疫微阵列

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摘要

Inductively coupled plasma mass spectrometry (ICPMS) has been successfully used for the detection of element-tagged biomolecules with the advantage of multielement capability. However, this technique cannot be used for microarray detection due to the necessity to dissolve the elemental tags before introducing them to the plasma source. Here, we report the detection of multiple proteins on each spot of the immuno-microarray by laser ablation ICPMS. alpha-Fetoprotein IgG (AFP), carcinoembryonic antigen (CEA), and human IgG, as model proteins, have been detected on the basis of sandwich-type immunoreactions on a microarray with Sm3+-labeled AFP antibody, Eu3+-labeled CEA antibody, and Au-labeled goat-anti-human IgG (GAH) as labeled antibodies. The detection limits were 0.20, 0.14, and 0.012 ng mL(-1) (3 sigma) with the RSD of 5.7%, 2.6%, and 2.3% at the concentration of 1.0 ng mL(-1) for AFP, CEA, and human IgG, respectively. The present detection method permits detecting multiple analytes from each spot of microarray with a spatial resolution at micrometer range, which can alleviate the stress to fabricate high-density arrays. Furthermore, the substrate materials and immobilized proteins do not interfere with the detection. The present technique provides a new strategy for readout of microarray.
机译:感应耦合等离子体质谱(ICPMS)已被成功用于元素标记生物分子的检测,并具有多元素分析的优势。但是,由于在将元素标签引入血浆源之前必须先溶解元素标签,因此该技术无法用于微阵列检测。在这里,我们报告通过激光消融ICPMS在免疫微阵列的每个斑点上检测到多种蛋白质。基于Sm3 +标记的AFP抗体,Eu3 +标记的CEA抗体和Sm3 +标记的微阵列上的三明治型免疫反应,已检测到甲胎蛋白IgG(AFP),癌胚抗原(CEA)和人IgG作为模型蛋白。 Au标记的山羊抗人IgG(GAH)作为标记的抗体。 AFP,CEA和AFP的检测限分别为0.20、0.14和0.012 ng mL(-1)(3 sigma),相对标准偏差为5.7%,2.6%和2.3%。人IgG。本发明的检测方法允许以微米范围的空间分辨率从微阵列的每个点检测多种分析物,这可以减轻制造高密度阵列的压力。此外,底物材料和固定的蛋白质不会干扰检测。本技术提供了读出微阵列的新策略。

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