Human Tissue Profiling with Multidimensional Protein Identification Technology
- 7 July 2005
- journal article
- Published by American Chemical Society (ACS) in Journal of Proteome Research
- Vol. 4 (5) , 1757-1767
- https://doi.org/10.1021/pr0500354
Abstract
Profiling of tissues and cell types through systematic characterization of expressed genes or proteins shows promise as a basic research tool, and has potential applications in disease diagnosis and classification. We used multidimensional protein identification protein identification technology (MudPIT) to analyze proteomes for enriched nuclear extracts of eight human tissues: brain, heart, liver, lung, muscle, pancreas, spleen, and testis. We show that the method is approximately 80% reproducible. We address issues of relative abundance, tissue-specificity, and selectivity, and the significance of proteins whose expression does not correlate with that of the corresponding mRNA. Surprisingly, most proteins are detected in a single tissue. These proteins tend to fulfill specialist (and potentially tissue-specific) functions compared to proteins expressed in two or more tissues. Keywords: proteomics • mass spectrometry • bioinformatics • tissue specificityKeywords
This publication has 34 references indexed in Scilit:
- The Human Proteome Organization Plasma Proteome Project pilot phase: Reference specimens, technology platform comparisons, and standardized data submissions and analysesProteomics, 2004
- Chromatin remodeling by ATP‐dependent molecular machinesBioEssays, 2003
- Genomic Imprinting: Intricacies of Epigenetic Regulation in ClustersAnnual Review of Cell and Developmental Biology, 2003
- Diversified transcription initiation complexes expand promoter selectivity and tissue-specific gene expressionGenes & Development, 2003
- Global functional profiling of gene expression☆☆This work was funded in part by a Sun Microsystems grant awarded to S.D., NIH Grant HD36512 to S.A.K., a Wayne State University SOM Dean’s Post-Doctoral Fellowship, and an NICHD Contraception and Infertility Loan to G.C.O. Support from the WSU MCBI mode is gratefully appreciated.Genomics, 2003
- Analyzing yeast protein–protein interaction data obtained from different sourcesNature Biotechnology, 2002
- Analysis of the Plasmodium falciparum proteome by high-accuracy mass spectrometryNature, 2002
- A proteomic view of the Plasmodium falciparum life cycleNature, 2002
- Analysis of mRNA expression and protein abundance data: an approach for the comparison of the enrichment of features in the cellular population of proteins and transcriptsBioinformatics, 2002
- Expression monitoring by hybridization to high-density oligonucleotide arraysNature Biotechnology, 1996