Yeast Expression Proteomics by High-resolution Mass Spectrometry
Overview
Affiliations
Comprehensive analysis of yeast as a model system requires to reliably determine its composition. Systematic approaches to globally determine the abundance of RNAs have existed for more than a decade and measurements of mRNAs are widely used as proxies for detecting changes in protein abundance. In contrast, methodologies to globally quantitate proteins are only recently becoming available. Such experiments are essential as proteins mediate the majority of biological processes and their abundance does not always correlate well with changes in gene expression. Particularly translational and post-translational controls contribute majorly to regulation of protein abundance, for example in heat shock stress response. The development of new sample preparation methods, high-resolution mass spectrometry and novel bioinfomatic tools close this gap and allow the global quantitation of the yeast proteome under different conditions. Here, we provide background information on proteomics by mass-spectrometry and describe the practice of a comprehensive yeast proteome analysis.
Proteomics insights into DNA damage response and translating this knowledge to clinical strategies.
von Stechow L, Olsen J Proteomics. 2016; 17(3-4).
PMID: 27682984 PMC: 5333460. DOI: 10.1002/pmic.201600018.
Quantitation of Vacuolar Sugar Transporter Abundance Changes Using QconCAT Synthtetic Peptides.
Pertl-Obermeyer H, Trentmann O, Duscha K, Neuhaus H, Schulze W Front Plant Sci. 2016; 7:411.
PMID: 27148277 PMC: 4828444. DOI: 10.3389/fpls.2016.00411.
Adhikari J, Fitzgerald M J Am Soc Mass Spectrom. 2014; 25(12):2073-83.
PMID: 25315461 DOI: 10.1007/s13361-014-0992-y.
The emergence of proteome-wide technologies: systematic analysis of proteins comes of age.
Breker M, Schuldiner M Nat Rev Mol Cell Biol. 2014; 15(7):453-64.
PMID: 24938631 DOI: 10.1038/nrm3821.
A novel single-cell screening platform reveals proteome plasticity during yeast stress responses.
Breker M, Gymrek M, Schuldiner M J Cell Biol. 2013; 200(6):839-50.
PMID: 23509072 PMC: 3601363. DOI: 10.1083/jcb.201301120.