Analysis of protein expression in cell microarrays:: A tool for antibody-based proteomics

被引:56
作者
Andersson, Ann-Catrin
Stromberg, Sara
Backvall, Helena
Kampf, Caroline
Uhlen, Mathias
Wester, Kenneth
Ponten, Fredrik
机构
[1] Univ Uppsala Hosp, Dept Genet & Pathol, Rudbeck Lab, SE-75185 Uppsala, Sweden
[2] Royal Inst Technol, Dept Biotechnol, Stockholm, Sweden
关键词
immunohistochemistry; cell line; tissue microarray; affinity proteomics; antibody-based proteomics;
D O I
10.1369/jhc.6A7001.2006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
Tissue microarray (TMA) technology provides a possibility to explore protein expression patterns in a multitude of normal and disease tissues in a high-throughput setting. Although TMAs have been used for analysis of tissue samples, robust methods for studying in vitro cultured cell lines and cell aspirates in a TMA format have been lacking. We have adopted a technique to homogeneously distribute cells in an agarose gel matrix, creating an artificial tissue. This enables simultaneous profiling of protein expression in suspension- and adherent-grown cell samples assembled in a microarray. In addition, the present study provides an optimized strategy for the basic laboratory steps to efficiently produce TMAs. Presented modifications resulted in an improved quality of specimens and a higher section yield compared with standard TMA production protocols. Sections from the generated cell TMAs were tested for immunohistochemical staining properties using 20 well-characterized antibodies. Comparison of immunoreactivity in cultured dispersed cells and corresponding cells in tissue samples showed congruent results for all tested antibodies. We conclude that a modified TIVIA technique, including cell samples, provides a valuable tool for high-throughput analysis of protein expression, and that this technique can be used for global approaches to explore the human proteome.
引用
收藏
页码:1413 / 1423
页数:11
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