Mass spectrometric characterization of proteins from the SARS virus - A preliminary report

被引:142
|
作者
Krokhin, O
Li, Y
Andonov, A
Feldmann, H
Flick, R
Jones, S
Stroeher, U
Bastien, N
Dasuri, KVN
Cheng, KD
Simonsen, JN
Perreault, H
Wilkins, J
Ens, W
Plummer, F [1 ]
Standing, KG
机构
[1] Univ Manitoba, Dept Phys, Winnipeg, MB R3T 2N2, Canada
[2] Univ Manitoba, Dept Astron, Winnipeg, MB R3T 2N2, Canada
[3] Manitoba Ctr Proteom, Winnipeg, MB R3E 3P4, Canada
[4] Natl Microbiol Lab, Winnipeg, MB R3E 3R2, Canada
[5] Univ Manitoba, Dept Med Microbiol, Winnipeg, MB R3E OW3, Canada
[6] Univ Manitoba, Dept Chem, Winnipeg, MB R3T 2N2, Canada
关键词
D O I
10.1074/mcp.M300048-MCP200
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
new coronavirus has been implicated as the causative agent of severe acute respiratory syndrome (SARS). We have used convalescent sera from several SARS patients to detect proteins in the culture supernatants from cells exposed to lavage another SARS patient. The most prominent protein in the supernatant was identified by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) as a similar to46-kDa species. This was found to be a novel nucleocapsid protein that matched almost exactly one predicted by an open reading frame in the recently published nucleotide sequence of the same virus isolate (>96% coverage). A second viral protein corresponding to the predicted similar to139-kDa spike glycoprotein has also been examined by MALDI-TOF MS (42% coverage). After peptide N-glycosidase F digestion, 12 glycosylation sites in this protein were confirmed. The sugars attached to four of the sites were also identified. These results suggest that the nucleocapsid protein is a major immunogen that may be useful for early diagnostics, and that the spike glycoprotein may present a particularly attractive target for prophylactic intervention in combating SARS.
引用
收藏
页码:346 / 356
页数:11
相关论文
共 50 条
  • [1] Tandem mass spectrometric characterization of modified peptides and proteins
    Bolgar, MS
    Gaskell, SJ
    BIOCHEMICAL SOCIETY TRANSACTIONS, 1995, 23 (04) : 907 - 910
  • [2] Mass spectrometric characterization of proteins transferred from polyacrylamide gels to membrane filters
    Ino, Yoko
    Hirano, Hisashi
    FEBS JOURNAL, 2011, 278 (20) : 3807 - 3814
  • [3] Mass Spectrometric Characterization of Disulfide Bridges in Snake Venom Proteins
    Goyder, Miriam S.
    Pfeifer, Marc E.
    Kalman, Franka
    CHIMIA, 2014, 68 (03) : 184 - 184
  • [4] TANDEM MASS-SPECTROMETRIC CHARACTERIZATION OF MODIFIED PEPTIDES AND PROTEINS
    GASKELL, SJ
    JOURNAL OF PROTEIN CHEMISTRY, 1994, 13 (05): : 494 - 496
  • [5] EVALUATION OF MASS-SPECTROMETRIC TECHNIQUES FOR CHARACTERIZATION OF ENGINEERED PROTEINS
    ROEPSTORFF, P
    SCHRAM, KH
    ANDERSEN, JS
    RAFN, K
    BALDURSSON, T
    KROLL, J
    POULSEN, K
    KNUDSEN, J
    KRISTIANSEN, K
    MOLECULAR BIOTECHNOLOGY, 1995, 4 (01) : 1 - 12
  • [6] In-gel digestion for mass spectrometric characterization of proteins and proteomes
    Andrej Shevchenko
    Henrik Tomas
    Jan Havli
    Jesper V Olsen
    Matthias Mann
    Nature Protocols, 2006, 1 : 2856 - 2860
  • [7] Mass spectrometric characterization of microalgal proteins and secondary metabolites.
    Jones, AD
    Hironaka, JL
    Henley, WJ
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2000, 219 : U229 - U230
  • [8] In-gel digestion for mass spectrometric characterization of proteins and proteomes
    Shevchenko, Andrej
    Tomas, Henrik
    Havlis, Jan
    Olsen, Jesper V.
    Mann, Matthias
    NATURE PROTOCOLS, 2006, 1 (06) : 2856 - 2860
  • [9] AUTOMATIC MASS-SPECTROMETRIC ANALYSIS - PRELIMINARY REPORT ON DEVELOPMENT OF A NOVEL MASS-SPECTROMETRIC SYSTEM FOR BIOMEDICAL APPLICATIONS
    DREYER, WJ
    KUPPERMANN, A
    BOETTGER, HG
    GIFFIN, CE
    NORRIS, DD
    GROTCH, SL
    THEARD, LP
    CLINICAL CHEMISTRY, 1974, 20 (08) : 998 - 1002
  • [10] Mass spectrometric analysis of proteins
    Wilm, M
    ADVANCES IN PROTEIN CHEMISTRY, VOL 54: ANALYSIS OF AMINO ACID SEQUENCES, 2000, 54 : 1 - 30