PeptideAtlasapplication/xmlftp://ftp.peptideatlas.org/pub/PeptideAtlas/Repository/Human/PAe005275/PAe005275_prot_10302_201512311901.propertiesftp://ftp.peptideatlas.org/pub/PeptideAtlas/Repository/Human/PAe005275/PAe005275_Search_Results_10302_201512311901.tar.gzftp://ftp.peptideatlas.org/pub/PeptideAtlas/Repository/Human/PAe005275/PAe005275_mzXML_201512311858.propertiesftp://ftp.peptideatlas.org/pub/PeptideAtlas/Repository/Human/PAe005275/PAe005275_Search_Results_10302_201512311901.propertiesftp://ftp.peptideatlas.org/pub/PeptideAtlas/Repository/Human/PAe005275/PAe005275_READMEftp://ftp.peptideatlas.org/pub/PeptideAtlas/Repository/Human/PAe005275/PAe005275_prot_10302_201512311901.tar.gzftp://ftp.peptideatlas.org/pub/PeptideAtlas/Repository/Human/PAe005275/PAe005275_10302_tandem.paramsftp://ftp.peptideatlas.org/pub/PeptideAtlas/Repository/Human/PAe005275/PAe005275_mzXML_201512311858.tar.gzprimaryOK200Hanfa ZouTPP'https://db.systemsbiology.net/sbeams/cgi/PeptideAtlas/ManageTable.cgi?TABLE_NAME=AT_sample&sample_id=6547'OthersPeptideAtlasProteomicsLTQ Orbitrap XLHomo Sapiens (human)HeLaComplete coverage of all phosphorylation sites in a proteome is the ultimate goal for large-scale phosphoproteome analysis. However, only making use of one protease trypsin for protein digestion cannot cover all phosphorylation sites, because not all tryptic phosphopeptides are detectable in MS. To further increase the phosphoproteomics coverage of HeLa cells, we proposed a tandem digestion approach by using two different proteases. By combining the data set of the first Glu-C digestion and the second trypsin digestion, the tandem digestion approach resulted in the identification of 8062 unique phosphopeptides and 8507 phosphorylation sites in HeLa cells. The conventional trypsin digestion approach resulted in the identification of 3891 unique phosphopeptides and 4647 phosphorylation sites. It was found that the phosphorylation sites identified from the above two approaches were highly complementary. By combining above two data sets, in total we identified 10899 unique phosphopeptides and 11262 phosphorylation sites, corresponding to 3437 unique phosphoproteins with FDR < 1% at peptide level. We also compared the kinase motifs extracted from trypsin, Glu-C, or a second trypsin digestion data sets. It was observed that basophilic motifs were more frequently found in the trypsin and the second trypsin digestion data sets, and the acidic motifs were more frequently found in the Glu-C digestion data set. These results demonstrated that our tandem digestion approach is a good complement to the conventional trypsin digestion approach for improving the phosphoproteomics analysis coverage of HeLa cells.Improve the coverage for the analysis of phosphoproteome of HeLa cells by a tandem digestion approach.Bian Yangyang Y, Ye Mingliang M, Song Chunxia C, Cheng Kai K, Wang Chunli C, Wei Xiaoluan X, Zhu Jun J, Chen Rui R, Wang Fangjun F, Zou Hanfa HfalseHs_Hela_Phospho_GlucHs Hela Cell, Ti4+-IMAC phospho enrichment, Gluc 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