Hu Yuhui, Janitz Michal
The Berlin Institute for Medical Systems Biology, Max Delbrück Center for Molecular Medicine (MDC), Berlin-Buch, Germany.
Methods Mol Biol. 2011;706:53-72. doi: 10.1007/978-1-61737-970-3_5.
Knowledge of protein localization within the cellular environment is critical for understanding the function of the protein and its regulatory networks. Protein localization data, however, have traditionally been accumulated from single or small-scale experiments. Transfected-cell arrays (TCAs) represent a robust alternative for the high-throughput analysis of gene/protein functions in mammalian cells. For protein localization studies, TCAs not only allow for the transfection and expression of over 1,000 genes in a single experiment but also make it feasible for simultaneous co-localization analyses of different subcellular compartments. In this chapter, we have described a protein co-localization protocol using transfected human cell arrays for a large set of cellular compartments, including the nucleus, ER, Golgi apparatus, mitochondrion, lysosome, peroxisome, and the microtubules, intermediate filaments and actin filaments. The application of these "organelle-co-localized cell arrays" facilitates the precise determination of the localizations of numerous recombinant proteins in a single experiment, making it currently the most efficient technique for high-throughput protein co-localization screening.
了解蛋白质在细胞环境中的定位对于理解蛋白质的功能及其调控网络至关重要。然而,传统上蛋白质定位数据是通过单个或小规模实验积累的。转染细胞阵列(TCA)是对哺乳动物细胞中的基因/蛋白质功能进行高通量分析的一种强大替代方法。对于蛋白质定位研究,TCA不仅允许在单个实验中转染和表达1000多个基因,还使得对不同亚细胞区室进行同时共定位分析成为可能。在本章中,我们描述了一种使用转染的人类细胞阵列对大量细胞区室(包括细胞核、内质网、高尔基体、线粒体、溶酶体、过氧化物酶体以及微管、中间丝和肌动蛋白丝)进行蛋白质共定位的方案。这些“细胞器共定位细胞阵列”的应用有助于在单个实验中精确确定众多重组蛋白的定位,使其成为目前高通量蛋白质共定位筛选中最有效的技术。