Literature DB >> 27644430

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

Liu Yang, Zhihua Wang, Yuliang Deng, Yan Li1, Wei Wei2, Qihui Shi.   

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.

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Year:  2016        PMID: 27644430      PMCID: PMC5519775          DOI: 10.1021/acs.analchem.6b03086

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  28 in total

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2.  Ex vivo expansion of circulating lung tumor cells based on one-step microfluidics-based immunomagnetic isolation.

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3.  Chemical methods for the simultaneous quantitation of metabolites and proteins from single cells.

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4.  Multidimensional analysis of the frequencies and rates of cytokine secretion from single cells by quantitative microengraving.

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Journal:  Lab Chip       Date:  2010-04-08       Impact factor: 6.799

5.  Reproducible copy number variation patterns among single circulating tumor cells of lung cancer patients.

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  13 in total

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3.  Injection Molded Microfluidics for Establishing High-Density Single Cell Arrays in an Open Hydrogel Format.

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Review 4.  Deep Profiling of Cellular Heterogeneity by Emerging Single-Cell Proteomic Technologies.

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Review 5.  Single cell proteomics in biomedicine: High-dimensional data acquisition, visualization, and analysis.

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Journal:  Proteomics       Date:  2017-02       Impact factor: 3.984

Review 6.  The future of microfluidics in immune checkpoint blockade.

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7.  Microparticle Delivery of Protein Markers for Single-Cell Western Blotting from Microwells.

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8.  Perspective of Molecular Diagnosis in Healthcare: From Barcode to Pattern Recognition.

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Review 9.  Defining Cell Identity with Single-Cell Omics.

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Journal:  Proteomics       Date:  2018-05-28       Impact factor: 3.984

10.  Highly Multiplexed Single-Cell Protein Profiling with Large-Scale Convertible DNA-Antibody Barcoded Arrays.

Authors:  Peng Zhao; Sirsendu Bhowmick; Jianchao Yu; Jun Wang
Journal:  Adv Sci (Weinh)       Date:  2018-08-02       Impact factor: 16.806

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