On-chip, cell-based microarray immunofluorescence assay for high-throughput analysis of target proteins

被引:56
作者
Fernandes, Tiago G. [1 ,3 ]
Kwon, Seok-Joon [1 ]
Lee, Moo-Yeal [4 ]
Clark, Douglas S. [5 ]
Cabral, Joaquim M. S. [3 ]
Dordick, Jonathan S. [1 ,2 ]
机构
[1] Rensselaer Polytech Inst, Dept Chem & Biol Engn, Troy, NY 12180 USA
[2] Rensselaer Polytech Inst, Dept Biol, Troy, NY 12180 USA
[3] Inst Super Tecn, Ctr Biol & Chem Engn, IBB, P-1049001 Lisbon, Portugal
[4] Solidus Biosci Inc, Troy, NY 12180 USA
[5] Univ Calif Berkeley, Dept Chem Engn, Berkeley, CA 94720 USA
关键词
D O I
10.1021/ac800848j
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We have developed an immunofluorescence-based assay for high-throughput analysis of target proteins on a three-dimensional cellular microarray platform. This process integrates the use of three-dimensional cellular microarrays, which should better mimic the cellular microenvironment, with sensitive immunofluorescence detection and provides quantitative information on cell function. To demonstrate this assay platform, we examined the accumulation of the a subunit of the hypoxia-inducible factor (HIF-1 alpha) after chemical stimulation of human pancreatic tumor cells encapsulated in 3D alginate spots in volumes as low as 60 nL. We also tested the effect of the known dysregulator of HIF-1 alpha, 2-methoxyestradiol (2ME2), on the levels of HIF-1 alpha using a dual microarray stamping technique. Ibis chip-based in situ Western immunoassay protocol was able to provide quantitative information on cell function, namely, the cellular response to hypoxia mimicking conditions and the reduction of HIF-1 alpha levels after cell treatment with 2ME2. This system is the first to enable high-content screening of cellular protein levels on a 3D human cell microarray platform.
引用
收藏
页码:6633 / 6639
页数:7
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