Department of Chemistry, University of Oxford, South Parks Road, Oxford OX1 3QZ, U.K.
Department of Chemistry, University of Otago, Dunedin 9054, New Zealand.
Anal Chem. 2023 May 23;95(20):7906-7913. doi: 10.1021/acs.analchem.3c00357. Epub 2023 May 11.
The analysis of cargo proteins in exosome subpopulations has considerable value in diagnostics but a translatable impact has been limited by lengthy or complex exosome extraction protocols. We describe herein a scalable, fast, and low-cost exosome extraction using an alternating (AC) magnetic field to support the dynamic mixing of antibody-coated magnetic beads (MBs) with serum samples within 3D-printed microfluidic chips. Zwitterionic polymer-coated MBs are, specifically, magnetically agitated and support ultraclean exosome capture efficiencies >70% from <50 μL of neat serum in 30 min. Applied herein to the immunocapture of neuronal exosomes using anti-L1CAM antibodies, prior to the array-based assaying of α-synuclein (α-syn) content by a standard duplex electrochemical sandwich ELISA, sub pg/mL detection was possible with an excellent coefficient of variation and a sample-to-answer time of ∼75 min. The high performance and semiautomation of this approach hold promise in underpinning low-cost Parkinson's disease diagnostics and is of value in exosomal biomarker analyses more generally.
对外泌体亚群中货物蛋白的分析在诊断方面具有相当大的价值,但由于外泌体提取的方案冗长或复杂,其转化应用受到限制。在此,我们描述了一种可扩展、快速且低成本的外泌体提取方法,该方法使用交变(AC)磁场来支持抗体包被的磁珠(MB)与血清样本在 3D 打印微流控芯片内的动态混合。具体而言,两性离子聚合物包被的 MB 可通过磁场搅拌,在 30 分钟内从小于 50μL 的纯血清中,以>70%的超高纯度捕获外泌体。本文将其应用于使用抗 L1CAM 抗体对外泌体进行免疫捕获,然后通过标准的双电化学夹心 ELISA 对 α-突触核蛋白(α-syn)含量进行基于阵列的分析,该方法可以实现 sub pg/mL 的检测,具有出色的变异系数和约 75 分钟的样本分析时间。这种方法的高性能和半自动化有望为低成本帕金森病诊断提供支持,并且在外泌体生物标志物分析中具有价值。