Shotgun collision-induced dissociation of peptides using a time of flight mass analyzer

被引:145
作者
Purvine, S [1 ]
Eppel, JT [1 ]
Yi, EC [1 ]
Goodlett, DR [1 ]
机构
[1] Inst Syst Biol, Seattle, WA 98105 USA
关键词
in-source collision-induced dissociation; parallel peptide tandem mass spectrometry; peptide mixtures;
D O I
10.1002/pmic.200300362
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Parallel collision-induced dissociation (CID) of peptides rather than serial, as is customary, results in loss of the obvious parent-fragment ion lineage available from CID on a single ion. We report proof-of-principle results suggesting the feasibility of parallel peptide CID, referred to here as shotgun CID, for protein identification when using the measured mass accuracies available from a time of flight mass analyzer and currently available search routines such as SEQUEST Additionally, we report that parent-fragment ion lineage may be reconstructed from information encoded in the chromatographic single ion current traces of peptides.
引用
收藏
页码:847 / 850
页数:4
相关论文
共 16 条
[1]   Mass spectrometry in proteomics [J].
Aebersold, R ;
Goodlett, DR .
CHEMICAL REVIEWS, 2001, 101 (02) :269-295
[2]   AN APPROACH TO CORRELATE TANDEM MASS-SPECTRAL DATA OF PEPTIDES WITH AMINO-ACID-SEQUENCES IN A PROTEIN DATABASE [J].
ENG, JK ;
MCCORMACK, AL ;
YATES, JR .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 1994, 5 (11) :976-989
[3]   Protein identification with a single accurate mass of a cysteine-containing peptide and constrained database searching [J].
Goodlett, DR ;
Bruce, JE ;
Anderson, GA ;
Rist, B ;
Pasa-Tolic, L ;
Fiehn, O ;
Smith, RD ;
Aebersold, R .
ANALYTICAL CHEMISTRY, 2000, 72 (06) :1112-1118
[4]   Differential stable isotope labeling of peptides for quantitation and de novo sequence derivation [J].
Goodlett, DR ;
Keller, A ;
Watts, JD ;
Newitt, R ;
Yi, EC ;
Purvine, S ;
Eng, JK ;
von Haller, P ;
Aebersold, R ;
Kolker, E .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2001, 15 (14) :1214-1221
[5]   Quantitative analysis of complex protein mixtures using isotope-coded affinity tags [J].
Gygi, SP ;
Rist, B ;
Gerber, SA ;
Turecek, F ;
Gelb, MH ;
Aebersold, R .
NATURE BIOTECHNOLOGY, 1999, 17 (10) :994-999
[6]   Ser2194 is a highly conserved major phosphorylation site of the hepatitis C virus nonstructural protein NS5A [J].
Katze, MG ;
Kwieciszewski, B ;
Goodlett, DR ;
Blakely, CM ;
Neddermann, P ;
Tan, SL ;
Aebersold, R .
VIROLOGY, 2000, 278 (02) :501-513
[7]  
Lee N, 1998, J IMMUNOL, V160, P4951
[8]   Direct analysis of protein complexes using mass spectrometry [J].
Link, AJ ;
Eng, J ;
Schieltz, DM ;
Carmack, E ;
Mize, GJ ;
Morris, DR ;
Garvik, BM ;
Yates, JR .
NATURE BIOTECHNOLOGY, 1999, 17 (07) :676-682
[9]   Accurate mass multiplexed tandem mass spectrometry for high-throughput polypeptide identification from mixtures [J].
Masselon, C ;
Anderson, GA ;
Harkewicz, R ;
Bruce, JE ;
Pasa-Tolic, L ;
Smith, RD .
ANALYTICAL CHEMISTRY, 2000, 72 (08) :1918-1924
[10]   Direct analysis and identification of proteins in mixtures by LC/MS/MS and database searching at the low-femtomole level [J].
McCormack, AL ;
Schieltz, DM ;
Goode, B ;
Yang, S ;
Barnes, G ;
Drubin, D ;
Yates, JR .
ANALYTICAL CHEMISTRY, 1997, 69 (04) :767-776