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基于珠上条码抗体微阵列的稀有肿瘤细胞单细胞多重蛋白检测。

Single-Cell, Multiplexed Protein Detection of Rare Tumor Cells Based on a Beads-on-Barcode Antibody Microarray.

机构信息

Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai, People's Republic of China.

Department of Molecular and Medical Pharmacology, David Geffen School of Medicine, University of California, Los Angeles , Los Angeles, California, United States.

出版信息

Anal Chem. 2016 Nov 15;88(22):11077-11083. doi: 10.1021/acs.analchem.6b03086. Epub 2016 Sep 28.

DOI:10.1021/acs.analchem.6b03086
PMID:27644430
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5519775/
Abstract

Circulating tumor cells (CTCs) shed from tumor sites and represent the molecular characteristics of the tumor. Besides genetic and transcriptional characterization, it is important to profile a panel of proteins with single-cell precision for resolving CTCs' phenotype, organ-of-origin, and drug targets. We describe a new technology that enables profiling multiple protein markers of extraordinarily rare tumor cells at the single-cell level. This technology integrates a microchip consisting of 15000 60 pL-sized microwells and a novel beads-on-barcode antibody microarray (BOBarray). The BOBarray allows for multiplexed protein detection by assigning two independent identifiers (bead size and fluorescent color) of the beads to each protein. Four bead sizes (1.75, 3, 4.5, and 6 μm) and three colors (blue, green, and yellow) are utilized to encode up to 12 different proteins. The miniaturized BOBarray can fit an array of 60 pL-sized microwells that isolate single cells for cell lysis and the subsequent detection of protein markers. An enclosed 60 pL-sized microchamber defines a high concentration of proteins released from lysed single cells, leading to single-cell resolution of protein detection. The protein markers assayed in this study include organ-specific markers and drug targets that help to characterize the organ-of-origin and drug targets of isolated rare tumor cells from blood samples. This new approach enables handling a very small number of cells and achieves single-cell, multiplexed protein detection without loss of rare but clinically important tumor cells.

摘要

循环肿瘤细胞(CTCs)从肿瘤部位脱落,代表肿瘤的分子特征。除了遗传和转录特征分析外,对一组具有单细胞精度的蛋白质进行分析以解析 CTCs 的表型、起源器官和药物靶点也很重要。我们描述了一种新技术,可在单细胞水平上对极罕见肿瘤细胞的多个蛋白质标志物进行分析。该技术集成了一个由 15000 个 60pL 大小的微井组成的微芯片和一种新颖的珠上条码抗体微阵列(BOBarray)。BOBarray 通过将两个独立的珠标识符(珠的大小和荧光颜色)分配给每个蛋白质,实现了蛋白质的多重检测。使用四个珠大小(1.75、3、4.5 和 6μm)和三种颜色(蓝色、绿色和黄色)可对多达 12 种不同的蛋白质进行编码。微型 BOBarray 可适应排列有 60pL 大小微井的阵列,用于分离单细胞进行细胞裂解,以及随后检测蛋白质标志物。封闭的 60pL 大小微腔定义了从裂解的单细胞中释放的蛋白质的高浓度,从而实现了蛋白质检测的单细胞分辨率。本研究中检测的蛋白质标志物包括器官特异性标志物和药物靶点,有助于表征从血液样本中分离出的罕见肿瘤细胞的起源器官和药物靶点。这种新方法能够处理非常少量的细胞,并实现单细胞、多重蛋白质检测,而不会丢失罕见但具有临床重要性的肿瘤细胞。

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本文引用的文献

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Protein Counting in Single Cancer Cells.单个癌细胞中的蛋白质计数
单细胞蛋白质分析中收缩微通道与循环神经网络的发展
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