Fragmentation characteristics of collision-induced dissociation in MALDI TOF/TOF mass spectrometry

被引:38
作者
Khatun, Jainab
Ramkissoon, Kevin
Giddings, Morgan C. [1 ]
机构
[1] Univ N Carolina, Dept Microbiol & Immunol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Comp Sci, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Joint Dept Biomed Engn, Chapel Hill, NC 27599 USA
[4] N Carolina State Univ, Raleigh, NC 27695 USA
关键词
D O I
10.1021/ac061455v
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The identification of proteins by tandem mass spectrometry relies on knowledge of the products produced by collision-induced dissociation of peptide ions. Most previous work has focused on fragmentation statistics for ion trap systems. We analyzed fragmentation in MALDI TOF/TOF mass spectrometry, collecting statistics using a curated set of 2459 MS/MS spectra and applying bootstrap resampling to assess confidence intervals. We calculated the frequency of 18 product ion types, the correlation between both mass and intensity with ion type, the dependence of amide bond breakage on the residues surrounding the cleavage site, and the dependence of product ion detection on residues not adjacent to the cleavage site. The most frequently observed were internal ions, followed by y ions. A strong correlation between ion type and the mass and intensity of its peak was observed, with b and y ions producing the most intense and highest mass peaks. The amino acids P, W, D, and R had a strong effect on amide bond cleavage when situated next to the breakage site, whereas residues including I, K, and H had a strong effect on product ion observation when located in the peptide but not adjacent to the cleavage site, a novel observation.
引用
收藏
页码:3032 / 3040
页数:9
相关论文
共 34 条
[11]   Open mass spectrometry search algorithm [J].
Geer, LY ;
Markey, SP ;
Kowalak, JA ;
Wagner, L ;
Xu, M ;
Maynard, DM ;
Yang, XY ;
Shi, WY ;
Bryant, SH .
JOURNAL OF PROTEOME RESEARCH, 2004, 3 (05) :958-964
[12]   Automated protein identification by tandem mass spectrometry:: Issues and strategies [J].
Hernandez, P ;
Müller, M ;
Appel, RD .
MASS SPECTROMETRY REVIEWS, 2006, 25 (02) :235-254
[13]   Automated de novo sequencing of proteins by tandem high-resolution mass spectrometry [J].
Horn, DM ;
Zubarev, RA ;
McLafferty, FW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (19) :10313-10317
[14]   Statistical characterization of the charge state and residue dependence of low-energy CID peptide dissociation patterns [J].
Huang, YY ;
Triscari, JM ;
Tseng, GC ;
Pasa-Tolic, L ;
Lipton, MS ;
Smith, RD ;
Wysocki, VH .
ANALYTICAL CHEMISTRY, 2005, 77 (18) :5800-5813
[15]   Mining a tandem mass spectrometry database to determine the trends and global factors influencing peptide fragmentation [J].
Kapp, EA ;
Schütz, F ;
Reid, GE ;
Eddes, JS ;
Moritz, RL ;
O'Hair, RAJ ;
Speed, TP ;
Simpson, RJ .
ANALYTICAL CHEMISTRY, 2003, 75 (22) :6251-6264
[16]   ProSight PTM: an integrated environment for protein identification and characterization by top-down mass spectrometry [J].
LeDuc, RD ;
Taylor, GK ;
Kim, YB ;
Januszyk, TE ;
Bynum, LH ;
Sola, JV ;
Garavelli, JS ;
Kelleher, NL .
NUCLEIC ACIDS RESEARCH, 2004, 32 :W340-W345
[17]   PEAKS:: powerful software for peptide de novo sequencing by tandem mass spectrometry [J].
Ma, B ;
Zhang, KZ ;
Hendrie, C ;
Liang, CZ ;
Li, M ;
Doherty-Kirby, A ;
Lajoie, G .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2003, 17 (20) :2337-2342
[18]   ERROR TOLERANT IDENTIFICATION OF PEPTIDES IN SEQUENCE DATABASES BY PEPTIDE SEQUENCE TAGS [J].
MANN, M ;
WILM, M .
ANALYTICAL CHEMISTRY, 1994, 66 (24) :4390-4399
[19]   PolyPhred: Automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing [J].
Nickerson, DA ;
Tobe, VO ;
Taylor, SL .
NUCLEIC ACIDS RESEARCH, 1997, 25 (14) :2745-2751
[20]  
O'Hair RAJ, 2000, J MASS SPECTROM, V35, P1377, DOI 10.1002/1096-9888(200012)35:12<1377::AID-JMS83>3.0.CO