TY - JOUR
T1 - Interlaboratory study characterizing a yeast performance standard for benchmarking LC-MS platform performance
AU - Paulovich, Amanda G.
AU - Billheimer, Dean
AU - Ham, Amy Joan L.
AU - Vega-Montoto, Lorenzo
AU - Rudnick, Paul A.
AU - Tabb, David L.
AU - Wang, Pei
AU - Blackman, Ronald K.
AU - Bunk, David M.
AU - Cardasis, Helene L.
AU - Clauser, Karl R.
AU - Kinsinger, Christopher R.
AU - Schilling, Birgit
AU - Tegeler, Tony J.
AU - Variyath, Asokan Mulayath
AU - Wang, Mu
AU - Whiteaker, Jeffrey R.
AU - Zimmerman, Lisa J.
AU - Fenyo, David
AU - Carr, Steven A.
AU - Fisher, Susan J.
AU - Gibson, Bradford W.
AU - Mesri, Mehdi
AU - Neubert, Thomas A.
AU - Regnier, Fred E.
AU - Rodriguez, Henry
AU - Spiegelman, Cliff
AU - Stein, Stephen E.
AU - Tempst, Paul
AU - Liebler, Daniel C.
PY - 2010/2
Y1 - 2010/2
N2 - Optimal performance of LC-MS/MS platforms is critical to generating high quality proteomics data. Although individual laboratories have developed quality control samples, there is no widely available performance standard of biological complexity (and associated reference data sets) for benchmarking of platform performance for analysis of complex biological proteomes across different laboratories in the community. Individual preparations of the yeast Saccharomyces cerevisiae proteome have been used extensively by laboratories in the proteomics community to characterize LC-MS platform performance. The yeast proteome is uniquely attractive as a performance standard because it is the most extensively characterized complex biological proteome and the only one associated with several large scale studies estimating the abundance of all detectable proteins. In this study, we describe a standard operating protocol for large scale production of the yeast performance standard and offer aliquots to the community through the National Institute of Standards and Technology where the yeast proteome is under development as a certified reference material to meet the long term needs of the community. Using a series of metrics that characterize LC-MS performance, we provide a reference data set demonstrating typical performance of commonly used ion trap instrument platforms in expert laboratories; the results provide a basis for laboratories to benchmark their own performance, to improve upon current methods, and to evaluate new technologies. Additionally, we demonstrate how the yeast reference, spiked with human proteins, can be used to benchmark the power of proteomics platforms for detection of differentially expressed proteins at different levels of concentration in a complex matrix, thereby providing a metric to evaluate and minimize preanalytical and analytical variation in comparative proteomics experiments.
AB - Optimal performance of LC-MS/MS platforms is critical to generating high quality proteomics data. Although individual laboratories have developed quality control samples, there is no widely available performance standard of biological complexity (and associated reference data sets) for benchmarking of platform performance for analysis of complex biological proteomes across different laboratories in the community. Individual preparations of the yeast Saccharomyces cerevisiae proteome have been used extensively by laboratories in the proteomics community to characterize LC-MS platform performance. The yeast proteome is uniquely attractive as a performance standard because it is the most extensively characterized complex biological proteome and the only one associated with several large scale studies estimating the abundance of all detectable proteins. In this study, we describe a standard operating protocol for large scale production of the yeast performance standard and offer aliquots to the community through the National Institute of Standards and Technology where the yeast proteome is under development as a certified reference material to meet the long term needs of the community. Using a series of metrics that characterize LC-MS performance, we provide a reference data set demonstrating typical performance of commonly used ion trap instrument platforms in expert laboratories; the results provide a basis for laboratories to benchmark their own performance, to improve upon current methods, and to evaluate new technologies. Additionally, we demonstrate how the yeast reference, spiked with human proteins, can be used to benchmark the power of proteomics platforms for detection of differentially expressed proteins at different levels of concentration in a complex matrix, thereby providing a metric to evaluate and minimize preanalytical and analytical variation in comparative proteomics experiments.
UR - http://www.scopus.com/inward/record.url?scp=76649122499&partnerID=8YFLogxK
U2 - 10.1074/mcp.M900222-MCP200
DO - 10.1074/mcp.M900222-MCP200
M3 - Article
C2 - 19858499
AN - SCOPUS:76649122499
SN - 1535-9476
VL - 9
SP - 242
EP - 254
JO - Molecular and Cellular Proteomics
JF - Molecular and Cellular Proteomics
IS - 2
ER -