Research Center for Analytical Instrumentation, Institute of Cyber Systems and Control, State Key Laboratory of Industrial Control Technology, Zhejiang University, Hangzhou, 310027, Zhejiang, PR China; College of Life Sciences, Zhejiang University, Hangzhou, 310058, Zhejiang, PR China.
Research Center for Analytical Instrumentation, Institute of Cyber Systems and Control, State Key Laboratory of Industrial Control Technology, Zhejiang University, Hangzhou, 310027, Zhejiang, PR China.
Anal Chim Acta. 2019 Oct 17;1076:118-124. doi: 10.1016/j.aca.2019.05.034. Epub 2019 May 17.
The quantification of low concentration proteins can facilitate the discovery of some significant biomarkers, and provide us a more profound understanding of cell heterogeneity when applied to single cell analysis. However, most state-of- art single cell protein detection platforms are bulky, expensive and complicated. Here we report a simple and low cost microfluidic dPCR (digital polymerase chain reaction) chip-based proximity ligation assay (PLA) for the quantification of low concentration proteins. First, standard hCSTB (human cystatin B) protein was used to optimize the related experimental conditions. Comparing to ordinary PLA tests, the results showed that our method achieved femtomolar limit of detection (LOD) with a linear dynamic range over three to four orders of magnitude. Then human CD147 protein, a reported biomarker for hepatoma carcinoma, was detected in single HepG2 and L02 cells. The results showed that there were wide disparities in single cell CD147 abundance for both of the two cell lines. And the average CD147 protein content in single HepG2 cells displayed 2-fold increase in comparison to that in single L02 cells. Comparing to the research findings obtained at bulk level, our method can provide more useful information for diagnosis and targeted therapy of tumors.
定量检测低浓度蛋白质可以促进一些重要生物标志物的发现,并在单细胞分析中为我们提供更深入的细胞异质性理解。然而,大多数最先进的单细胞蛋白质检测平台体积庞大、昂贵且复杂。在这里,我们报告了一种简单且低成本的微流控数字 PCR(dPCR)芯片基于邻近连接分析(PLA)的方法,用于定量检测低浓度蛋白质。首先,使用标准 hCSTB(人胱抑素 B)蛋白优化了相关实验条件。与普通 PLA 测试相比,结果表明我们的方法实现了飞摩尔级别的检测限(LOD),线性动态范围超过三个数量级。然后,我们在单个 HepG2 和 L02 细胞中检测了人 CD147 蛋白,这是肝癌的一种报道生物标志物。结果表明,两种细胞系中单细胞 CD147 的丰度差异很大。与单细胞 L02 细胞相比,单细胞 HepG2 细胞中的平均 CD147 蛋白含量增加了 2 倍。与在 bulk 水平获得的研究结果相比,我们的方法可以为肿瘤的诊断和靶向治疗提供更有用的信息。