RNA Deep Sequencing as a Tool for Selection of Cell Lines for Systematic Subcellular Localization of All Human Proteins

被引:13
作者
Danielsson, Frida [1 ]
Wiking, Mikaela [1 ]
Mahdessian, Diana [1 ]
Skogs, Marie [1 ]
Blal, Hammou Ait [1 ]
Hjelmare, Martin [1 ]
Stadler, Charlotte [1 ]
Uhlen, Mathias [1 ,2 ]
Lundberg, Emma [1 ]
机构
[1] KTH Royal Inst Technol, Sci Life Lab, SE-17121 Stockholm, Sweden
[2] KTH Royal Inst Technol, Dept Prote, SE-10691 Stockholm, Sweden
关键词
antibody; Human Protein Atlas; Human Proteome Project; RNA sequencing; subcellular localization; PROTEOME; ATLAS; ESTABLISHMENT; TRANSCRIPTOME; GROWTH; TUMORS;
D O I
10.1021/pr3009308
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
One of the major challenges of a chromosome-centric proteome project is to explore in a systematic manner the potential proteins identified from the chromosomal genome sequence, but not yet characterized on a protein level. Here, we describe the use of RNA deep sequencing to screen human cell lines for RNA profiles and to use this information to select cell lines suitable for characterization of the corresponding gene product. In this manner, the subcellular localization of proteins can be analyzed systematically using antibody-based confocal microscopy. We demonstrate the usefulness of selecting cell lines with high expression levels of RNA transcripts to increase the likelihood of high quality immunofluorescence staining and subsequent successful subcellular localization of the corresponding protein. The results show a path to combine transcriptomics with affinity proteomics to characterize the proteins in a gene- or chromosome-centric manner.
引用
收藏
页码:299 / 307
页数:9
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