TY - JOUR
T1 - A comprehensive Candida albicans PeptideAtlas build enables deep proteome coverage
AU - Vialas, Vital
AU - Sun, Zhi
AU - Reales-Calderón, Jose A.
AU - Hernáez, María L.
AU - Casas, Vanessa
AU - Carrascal, Montserrat
AU - Abián, Joaquín
AU - Monteoliva, Lucía
AU - Deutsch, Eric W.
AU - Moritz, Robert L.
AU - Gil, Concha
N1 - Publisher Copyright:
© 2015 Elsevier B.V.
PY - 2016/1/10
Y1 - 2016/1/10
N2 - To provide new and expanded proteome documentation of the opportunistically pathogen Candida albicans, we have developed new protein extraction and analysis routines to provide a new, extended and enhanced version of the C. albicans PeptideAtlas. Two new datasets, resulting from experiments consisting of exhaustive subcellular fractionations and different growing conditions, plus two additional datasets from previous experiments on the surface and the secreted proteomes, have been incorporated to increase the coverage of the proteome. High resolution precursor mass spectrometry (MS) and ion trap tandem MS spectra were analyzed with three different search engines using a database containing allele-specific sequences. This approach, novel for a large-scale C. albicans proteomics project, was combined with the post-processing and filtering implemented in the Trans Proteomic Pipeline consistently used in the PeptideAtlas project and resulted in 49,372 additional peptides (3-fold increase) and 1630 more proteins (1.6-fold increase) identified in the new C. albicans PeptideAtlas with respect to the previous build. A total of 71,310 peptides and 4174 canonical (minimal non-redundant set) proteins (4115 if one protein per pair of alleles is considered) were identified representing 66% of the 6218 proteins in the predicted proteome. This makes the new PeptideAtlas build the most comprehensive C. albicans proteomics resource available and the only large-scale one with detections of individual alleles.
AB - To provide new and expanded proteome documentation of the opportunistically pathogen Candida albicans, we have developed new protein extraction and analysis routines to provide a new, extended and enhanced version of the C. albicans PeptideAtlas. Two new datasets, resulting from experiments consisting of exhaustive subcellular fractionations and different growing conditions, plus two additional datasets from previous experiments on the surface and the secreted proteomes, have been incorporated to increase the coverage of the proteome. High resolution precursor mass spectrometry (MS) and ion trap tandem MS spectra were analyzed with three different search engines using a database containing allele-specific sequences. This approach, novel for a large-scale C. albicans proteomics project, was combined with the post-processing and filtering implemented in the Trans Proteomic Pipeline consistently used in the PeptideAtlas project and resulted in 49,372 additional peptides (3-fold increase) and 1630 more proteins (1.6-fold increase) identified in the new C. albicans PeptideAtlas with respect to the previous build. A total of 71,310 peptides and 4174 canonical (minimal non-redundant set) proteins (4115 if one protein per pair of alleles is considered) were identified representing 66% of the 6218 proteins in the predicted proteome. This makes the new PeptideAtlas build the most comprehensive C. albicans proteomics resource available and the only large-scale one with detections of individual alleles.
KW - Candida albicans
KW - Mass spectrometry
KW - PeptideAtlas
KW - Peptides
KW - Proteome
KW - Proteotypic
UR - http://www.scopus.com/inward/record.url?scp=84948160771&partnerID=8YFLogxK
U2 - 10.1016/j.jprot.2015.10.019
DO - 10.1016/j.jprot.2015.10.019
M3 - Article
C2 - 26493587
AN - SCOPUS:84948160771
SN - 1874-3919
VL - 131
SP - 122
EP - 130
JO - Journal of Proteomics
JF - Journal of Proteomics
ER -