Deep proteome and transcriptome mapping of a human cancer cell line

被引:772
作者
Nagaraj, Nagarjuna [1 ]
Wisniewski, Jacek R. [1 ]
Geiger, Tamar [1 ]
Cox, Juergen [1 ]
Kircher, Martin [2 ]
Kelso, Janet [2 ]
Paeaebo, Svante [2 ]
Mann, Matthias [1 ]
机构
[1] Max Planck Inst Biochem, Dept Prote & Signal Transduct, D-82152 Martinsried, Germany
[2] Max Planck Inst Evolutionary Anthropol, Dept Evolutionary Genet, Leipzig, Germany
关键词
mass spectrometry; proteomics; RNA-Seq; systems biology; transcriptomics; RNA-SEQ; HIGH-RESOLUTION; QUANTIFICATION; REVEALS; FRACTIONATION; DEPTH; TOOL;
D O I
10.1038/msb.2011.81
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
While the number and identity of proteins expressed in a single human cell type is currently unknown, this fundamental question can be addressed by advanced mass spectrometry (MS)-based proteomics. Online liquid chromatography coupled to high-resolution MS and MS/MS yielded 166 420 peptides with unique amino-acid sequence from HeLa cells. These peptides identified 10 255 different human proteins encoded by 9207 human genes, providing a lower limit on the proteome in this cancer cell line. Deep transcriptome sequencing revealed transcripts for nearly all detected proteins. We calculate copy numbers for the expressed proteins and show that the abundances of >90% of them are within a factor 60 of the median protein expression level. Comparisons of the proteome and the transcriptome, and analysis of protein complex databases and GO categories, suggest that we achieved deep coverage of the functional transcriptome and the proteome of a single cell type. Molecular Systems Biology 7: 548; published online 8 November 2011; doi:10.1038/msb.2011.81
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页数:8
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