Whole proteome analysis of post-translational modifications: Applications of mass-spectrometry for proteogenomic annotation

被引:158
作者
Gupta, Nitin [1 ]
Tanner, Stephen
Jaitly, Navdeep
Adkins, Joshua N.
Lipton, Mary
Edwards, Robert
Romine, Margaret
Osterman, Andrei
Bafna, Vineet
Smith, Richard D.
Pevzner, Pavel A.
机构
[1] Univ Calif San Diego, Bioinformat Program, La Jolla, CA 92039 USA
[2] Pacific NW Natl Lab, Div Biol Sci, Richland, WA 99352 USA
[3] Burnham Inst Med Res, La Jolla, CA 92037 USA
[4] Fellowship Interpretat Genomes, Burr Ridge, IL 60527 USA
[5] San Diego State Univ, San Diego, CA 92182 USA
[6] Univ Calif San Diego, Dept Comp Sci & Engn, La Jolla, CA 92093 USA
关键词
D O I
10.1101/gr.6427907
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
While bacterial genome annotations have significantly improved in recent years, techniques for bacterial proteome annotation (including post-translational chemical modifications, signal peptides, proteolytic events, etc.) are still in their infancy. At the same time, the number of sequenced bacterial genomes is rising sharply, far outpacing our ability to validate the predicted genes, let alone annotate bacterial proteomes. In this study, we use tandem mass spectrometry (MS/MS) to annotate the proteome of Shewanella oneidensis MR-1, an important microbe for bioremediation. In particular, we provide the first comprehensive map of post-translational modifications in a bacterial genome, including a large number of chemical modifications, signal peptide cleavages, and cleavages of N-terminal methionine residues. We also detect multiple genes that were missed or assigned incorrect start positions by gene prediction programs, and suggest corrections to improve the gene annotation. This study demonstrates that complementing every genome sequencing project by an MS/MS project would significantly improve both genome and proteome annotations for a reasonable cost.
引用
收藏
页码:1362 / 1377
页数:16
相关论文
共 91 条
[1]   Mass spectrometry-based proteomics [J].
Aebersold, R ;
Mann, M .
NATURE, 2003, 422 (6928) :198-207
[2]   A proteomic view on genome-based signal peptide predictions [J].
Antelmann, H ;
Tjalsma, H ;
Voigt, B ;
Ohlmeier, S ;
Bron, S ;
van Dijl, JM ;
Hecker, M .
GENOME RESEARCH, 2001, 11 (09) :1484-1502
[3]   Observation of Escherichia coli ribosomal proteins and their posttranslational modifications by mass spectrometry [J].
Arnold, RJ ;
Reilly, JP .
ANALYTICAL BIOCHEMISTRY, 1999, 269 (01) :105-112
[4]   Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants:: the Keio collection [J].
Baba, Tomoya ;
Ara, Takeshi ;
Hasegawa, Miki ;
Takai, Yuki ;
Okumura, Yoshiko ;
Baba, Miki ;
Datsenko, Kirill A. ;
Tomita, Masaru ;
Wanner, Barry L. ;
Mori, Hirotada .
MOLECULAR SYSTEMS BIOLOGY, 2006, 2 (1) :2006.0008
[5]   RECODE 2003 [J].
Baranov, PV ;
Gurvich, OL ;
Hammer, AW ;
Gesteland, RF ;
Atkins, JF .
NUCLEIC ACIDS RESEARCH, 2003, 31 (01) :87-89
[6]   Recoding: translational bifurcations in gene expression [J].
Baranov, PV ;
Gesteland, RF ;
Atkins, JF .
GENE, 2002, 286 (02) :187-201
[7]   PROCESSING OF THE INITIATION METHIONINE FROM PROTEINS - PROPERTIES OF THE ESCHERICHIA-COLI METHIONINE AMINOPEPTIDASE AND ITS GENE STRUCTURE [J].
BENBASSAT, A ;
BAUER, K ;
CHANG, SY ;
MYAMBO, K ;
BOOSMAN, A ;
CHANG, S .
JOURNAL OF BACTERIOLOGY, 1987, 169 (02) :751-757
[8]   Improved prediction of signal peptides: SignalP 3.0 [J].
Bendtsen, JD ;
Nielsen, H ;
von Heijne, G ;
Brunak, S .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 340 (04) :783-795
[9]   GenBank [J].
Benson, Dennis A. ;
Karsch-Mizrachi, Ilene ;
Lipman, David J. ;
Ostell, James ;
Wheeler, David L. .
NUCLEIC ACIDS RESEARCH, 2006, 34 :D16-D20
[10]   GeneMark: web software for gene finding in prokaryotes, eukaryotes and viruses [J].
Besemer, J ;
Borodovsky, M .
NUCLEIC ACIDS RESEARCH, 2005, 33 :W451-W454