利用液滴微流控技术同时检测单个细胞外囊泡水平的膜蛋白和 mRNA,用于癌症诊断。

Huixian Lin, Bo Li, Jingyun Guo, Xueying Mai, Haiyang Yu, Weilun Pan, Bodeng Wu, Wei Liu, Mingzhen Zhong, Tong Liao, Ye Zhang, Bo Situ, Xiaohui Yan, Yifan Liu, Chunchen Liu, Lei Zheng
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引用次数: 0

摘要

简介同时检测单个细胞外囊泡 (EV) 中的蛋白质和 mRNA 可对特定 EVs 亚群进行全面分析,从而大大推动癌症诊断。然而,开发一种灵敏且易于使用的方法来同时检测单个细胞外囊泡中的多维生物标记物仍具有挑战性:为了促进对 EV 中多维生物标志物的分析并推动其临床应用,我们提出了一种多功能液滴数字系统,可在单个 EV 水平同时检测膜蛋白和 mRNA,并具有高灵敏度和特异性:方法:首先制备抗体-DNA共轭物,用于EVs蛋白生物标志物的识别和信号转换。方法:首先制备了用于 EV 蛋白生物标志物识别和信号转化的抗体-DNA 结合物,然后将其与组装好的三重液滴数字 PCR 系统相结合,开发了一种多功能液滴数字分析检测方法,用于在单个 EV 水平上同时检测膜蛋白和 mRNA:结果:我们的新型液滴数字系统具有很高的灵敏度和特异性。结果:我们的新型液滴数字系统显示出较高的灵敏度和特异性,此外,其临床应用在乳腺癌队列中也得到了验证。正如预期的那样,通过联合检测 EVs 蛋白质和 mRNA 标记物,该检测方法在区分乳腺癌与健康人和良性对照组方面的表现优于任何单一种类标记物的检测,尤其是对于早期乳腺癌患者(AUC=0.9229):因此,本研究提出了一种很有前景的策略,即通过在单个 EV 水平联合检测蛋白质和 mRNA,准确识别和分析特定 EV 亚群,为未来的临床应用提供了巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Simultaneous detection of membrane protein and mRNA at single extracellular vesicle level by droplet microfluidics for cancer diagnosis.

Introduction: Simultaneous detection of proteins and mRNA within a single extracellular vesicle (EV) enables comprehensive analysis of specific EVs subpopulations, significantly advancing cancer diagnostics. However, developing a sensitive and user-friendly approach for simultaneously detecting multidimensional biomarkers in single EV is still challenging.

Objectives: To facilitate the analysis of multidimensional biomarkers in EVs and boost its clinical application, we present a versatile droplet digital system facilitating the concurrent detection of membrane proteins and mRNA at the single EV level with high sensitivity and specificity.

Methods: The antibody-DNA conjugates were firstly prepared for EVs protein biomarkers recognition and signal transformation. Coupling with the assembled triplex droplet digital PCR system, a versatile droplet digital analysis assay for simultaneous detection of membrane protein and mRNA at a single EV level was developed.

Results: Our new droplet digital system displayed high sensitivity and specificity. Additionally, its clinical application was validated in a breast cancer cohort. As expected, this assay has demonstrated superior performance in distinguishing breast cancer from healthy individuals and benign controls through combined detection of EVs protein and mRNA markers compared to any single kind marker detections, especially for patients with breast cancer at early stage (AUC=0.9229).

Conclusion: Consequently, this study proposes a promising strategy for accurately identifying and analyzing specific EV subgroups through the co-detection of proteins and mRNA at the single EV level, holding significant potential for future clinical applications.

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