Microfluidic Analyzer Enabling Quantitative Measurements of Specific Intracellular Proteins at the Single-Cell Level

被引:2
|
作者
Liu, Lixing [1 ,2 ]
Fan, Beiyuan [1 ,2 ]
Wang, Diancan [3 ]
Li, Xiufeng [1 ,2 ]
Song, Yeqing [3 ]
Zhang, Ting [1 ,2 ]
Chen, Deyong [1 ,2 ]
Wang, Yixiang [3 ]
Wang, Junbo [1 ,2 ]
Chen, Jian [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Elect, State Key Lab Transducer Technol, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100190, Peoples R China
[3] Peking Univ, Sch Stomatol, Beijing 10081, Peoples R China
来源
MICROMACHINES | 2018年 / 9卷 / 11期
基金
中国国家自然科学基金;
关键词
instrumentation; microfluidic flow cytometry; intracellular proteins; absolute quantification; FLOW-CYTOMETRY; HETEROGENEITY;
D O I
10.3390/mi9110588
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This paper presents a microfluidic instrument capable of quantifying single-cell specific intracellular proteins, which are composed of three functioning modules and two software platforms. Under the control of a LabVIEW platform, a pressure module flushed cells stained with fluorescent antibodies through a microfluidic module with fluorescent intensities quantified by a fluorescent module and translated into the numbers of specific intracellular proteins at the single-cell level using a MATLAB platform. Detection ranges and resolutions of the analyzer were characterized as 896.78-6.78 x 10(5) and 334.60 nM for Alexa 488, 314.60-2.11 x 10(5) and 153.98 nM for FITC, and 77.03-5.24 x 10(4) and 37.17 nM for FITC-labelled anti-beta-actin antibodies. As a demonstration, the numbers of single-cell beta-actins of two paired oral tumor cell types and two oral patient samples were quantified as: 1.12 +/- 0.77 x 10(6)/cell (salivary adenoid cystic carcinoma parental cell line (SACC-83), n(cell) = 13,689) vs. 0.90 +/- 0.58 x 10(5)/cell (salivary adenoid cystic carcinoma lung metastasis cell line (SACC-LM), n(cell) = 15,341); 0.89 +/- 0.69 x 10(6)/cell (oral carcinoma cell line (CAL 27), n(cell) = 7357) vs. 0.93 +/- 0.69 x 10(6)/cell (oral carcinoma lymphatic metastasis cell line (CAL 27-LN2), n(cell) = 6276); and 0.86 +/- 0.52 x 10(6)/cell (patient I) vs. 0.85 +/- 0.58 x 10(6)/cell (patient II). These results (1) validated the developed analyzer with a throughput of 10 cells/s and a processing capability of similar to 10,000 cells for each cell type, and (2) revealed that as an internal control in cell analysis, the expressions of beta-actins remained stable in oral tumors with different malignant levels.
引用
收藏
页数:9
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