Department of Chemistry, University of Connecticut, Storrs, Connecticut, United States.
Anal Chem. 2012 Jul 17;84(14):6249-55. doi: 10.1021/ac301392g. Epub 2012 Jul 3.
Multiplexed biomarker protein detection holds unrealized promise for clinical cancer diagnostics due to lack of suitable measurement devices and lack of rigorously validated protein panels. Here we report an ultrasensitive electrochemical microfluidic array optimized to measure a four-protein panel of biomarker proteins, and we validate the protein panel for accurate oral cancer diagnostics. Unprecedented ultralow detection into the 5-50 fg·mL(-1) range was achieved for simultaneous measurement of proteins interleukin 6 (IL-6), IL-8, vascular endothelial growth factor (VEGF), and VEGF-C in diluted serum. The immunoarray achieves high sensitivity in 50 min assays by using off-line protein capture by magnetic beads carrying 400,000 enzyme labels and ~100,000 antibodies. After capture of the proteins and washing to inhibit nonspecific binding, the beads are magnetically separated and injected into the array for selective capture by antibodies on eight nanostructured sensors. Good correlations with enzyme-linked immunosorbent assays (ELISA) for protein determinations in conditioned cancer cell media confirmed the accuracy of this approach. Normalized means of the four protein levels in 78 oral cancer patient serum samples and 49 controls gave clinical sensitivity of 89% and specificity of 98% for oral cancer detection, demonstrating high diagnostic utility. The low-cost, easily fabricated immunoarray provides a rapid serum test for diagnosis and personalized therapy of oral cancer. The device is readily adaptable to clinical diagnostics of other cancers.
由于缺乏合适的测量设备和经过严格验证的蛋白质组学,多重生物标志物蛋白检测在临床癌症诊断中尚未得到实现。在这里,我们报告了一种超灵敏的电化学微流控阵列,该阵列经过优化可用于测量四种生物标志物蛋白的蛋白质组学,并且我们验证了该蛋白质组学在口腔癌诊断中的准确性。通过使用带有 40 万个酶标记和约 10 万个抗体的磁性珠离线捕获蛋白质,同时在稀释的血清中测量白细胞介素 6 (IL-6)、IL-8、血管内皮生长因子 (VEGF) 和 VEGF-C,该免疫阵列在 50 分钟的测定中实现了前所未有的超低检测下限至 5-50 fg·mL(-1)。在捕获蛋白质并洗涤以抑制非特异性结合之后,将珠通过磁性分离并注入阵列中,通过八个纳米结构传感器上的抗体进行选择性捕获。在条件培养基中进行蛋白质测定的酶联免疫吸附测定 (ELISA) 与该方法的相关性良好,证实了该方法的准确性。78 例口腔癌患者血清样本和 49 例对照者的四种蛋白质水平的归一化平均值为口腔癌检测提供了 89%的临床灵敏度和 98%的特异性,证明了其具有较高的诊断实用性。该低成本、易于制造的免疫阵列提供了一种用于诊断和个性化治疗口腔癌的快速血清检测方法。该设备易于适应其他癌症的临床诊断。