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1.
Mol Cell Proteomics ; 12(6): 1741-51, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23462206

ABSTRACT

We report a high quality and system-wide proteome catalogue covering 71% (3,542 proteins) of the predicted genes of fission yeast, Schizosaccharomyces pombe, presenting the largest protein dataset to date for this important model organism. We obtained this high proteome and peptide (11.4 peptides/protein) coverage by a combination of extensive sample fractionation, high resolution Orbitrap mass spectrometry, and combined database searching using the iProphet software as part of the Trans-Proteomics Pipeline. All raw and processed data are made accessible in the S. pombe PeptideAtlas. The identified proteins showed no biases in functional properties and allowed global estimation of protein abundances. The high coverage of the PeptideAtlas allowed correlation with transcriptomic data in a system-wide manner indicating that post-transcriptional processes control the levels of at least half of all identified proteins. Interestingly, the correlation was not equally tight for all functional categories ranging from r(s) >0.80 for proteins involved in translation to r(s) <0.45 for signal transduction proteins. Moreover, many proteins involved in DNA damage repair could not be detected in the PeptideAtlas despite their high mRNA levels, strengthening the translation-on-demand hypothesis for members of this protein class. In summary, the extensive and publicly available S. pombe PeptideAtlas together with the generated proteotypic peptide spectral library will be a useful resource for future targeted, in-depth, and quantitative proteomic studies on this microorganism.


Subject(s)
Gene Expression Regulation, Fungal , Peptides/isolation & purification , Protein Processing, Post-Translational , Proteome/metabolism , RNA, Messenger/metabolism , Schizosaccharomyces pombe Proteins/metabolism , Schizosaccharomyces/metabolism , Databases, Protein , Mass Spectrometry , Multigene Family , Peptide Mapping , Proteome/chemistry , Proteome/genetics , RNA, Messenger/genetics , Schizosaccharomyces/chemistry , Schizosaccharomyces/genetics , Schizosaccharomyces pombe Proteins/chemistry , Schizosaccharomyces pombe Proteins/genetics , Signal Transduction
2.
Proteomics ; 6(10): 3176-88, 2006 May.
Article in English | MEDLINE | ID: mdl-16622891

ABSTRACT

In the present study, profiles of protein expression were examined during early development of zebrafish, an increasingly popular experimental model in vertebrate development and human diseases. By 2-DE, an initial increase in protein spots from 6 h post-fertilization (hpf) to 8-10 hpf was observed. There was no dramatic change in protein profiles up to 18 hpf, but significant changes occurred in subsequent stages. Interestingly, 49% of the proteins detected at 6 hpf remained detectable by 1 week of age. To map the protein expression patterns in 2-D gels, MALDI-TOF/TOF MS was employed to identify selected protein spots from early embryos. 108 protein spots were found to match known proteins and they were derived from 55 distinct genes. Interestingly, 11 (20%) of them produced multiple protein isoforms or distinct cleavage products. Although deyolked embryos were used in the analysis, a large number of vitellogenin derivatives remained prominently present in the embryos. Other than these, most of the identified proteins are cytosolic, cytoskeletal and nuclear proteins, which are involved in diversified functions such as metabolism, cytoskeleton, translation, protein degradation, etc. Some of the proteins with interesting temporal expression profiles during development are further discussed.


Subject(s)
Zebrafish Proteins/biosynthesis , Zebrafish/metabolism , Animals , Electrophoresis, Gel, Two-Dimensional , Embryo, Nonmammalian/metabolism , Gastrula/metabolism , Heat-Shock Proteins/biosynthesis , Keratins/biosynthesis , Larva , Protein Isoforms/biosynthesis , Proteomics , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization , Vitellogenins/biosynthesis , Zebrafish/embryology , Zebrafish/growth & development
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