Special Feature

User Panel

My Panel

My Panel

Bookmark Science Articles

Recent News
Bookmark / Share This Science Site

Protein identification via ion-trap collision-induced dissociation and examination of low-mass product ions.

Protein identification via ion-trap collision-induced dissociation and examination of low-mass product ions. Research Abstract Details 

Research Abstract Table of Contents

Jump to the:

  • Abstract Text of This Paper
  • Journal Published
  • MeSH Keywords of This Abstract
  • Chemicals and Substances Used in this Paper
  • Grants and Granting Agency of this Research
  • Database Accession Numbers Used in this Paper
  • Related Papers
  • Related Research Tags
  • Rate this Research Paper
  • Protein identification via ion-trap collision-induced dissociation and examination of low-mass product ions. Abstract Text:

    jeremiah j bowersJeremiah J Bowers,jian liuJian Liu,harsha p gunawardenaHarsha P Gunawardena,scott a mcluckeyScott A McLuckey,

    A whole-protein tandem mass spectrometry approach for protein identification based on precursor ion charge state concentration via ion/ion reactions, ion-trap collisional activation, ion/ion proton-transfer reactions involving the product ions, and mass analysis over a narrow m/z range (up to m/z 2000) is described and evaluated. The experiments were carried out with a commercially available electrospray ion-trap instrument that has been modified to allow for ion/ion reactions. Reaction conditions and the approach to searching protein databases were developed with the assumption that the resolving power of the mass analyzer is insufficient to distinguish charge states on the basis of the isotope spacings. Ions derived from several charge states of cytochrome c, myoglobin, ribonuclease A, and ubiquitin were used to evaluate the approach for protein identification and to develop a two-step procedure to database searching to optimize specificity. The approach developed with the model proteins was then applied to whole cell lysate fractions of Saccharomyces cerevisiae. The results are illustrated with examples of assignments made for three a priori unknown proteins, each selected randomly from a lysate fraction. Two of the three proteins were assigned to species present in the database, whereas one did not match well any database entry. The combination of the mass measurement and the product ion masses suggested the possibility for the oxidation of two methionine residues of a protein in the database. The examples show that this limited whole-protein characterization approach can provide insights that might otherwise be lacking with approaches based on complete enzymatic digestion. Copyright (c) 2007 John Wiley & Sons, Ltd.

    Protein identification via ion-trap collision-induced dissociation and examination of low-mass product ions. Publishing Authors By Initials

    jj bowersJJ Bowers,j liuJ Liu,hp gunawardenaHP Gunawardena,sa mcluckeySA McLuckey,

    For similar abstracts research abstracts see: abstracts research

    PUBMED ID PMID:

    MEDLINE DATE:

    Protein identification via ion-trap collision-induced dissociation and examination of low-mass product ions. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Journal of mass spectrometry : JMS

    VOLUME: 43

    Page Numbers: 23-34

    Journal Abbreviation:

    ISSN: 1076-5174

    DAY: 23

    MONTH: Jan

    YEAR: 2008

    Protein identification via ion-trap collision-induced dissociation and examination of low-mass product ions. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9504818

    Protein identification via ion-trap collision-induced dissociation and examination of low-mass product ions. Keywords Mesh Terms:

    KEYWORDS:

    MESH TERMS:

    Chemical & Substance for Abstract: Protein identification via ion-trap collision-induced dissociation and examination of low-mass product ions. Information

    Substance Name:

    Registry Number:

    Grant and Affiliation Information for Protein identification via ion-trap collision-induced dissociation and examination of low-mass product ions.

    AFFILIATION: Department of Chemistry, Purdue University, 560 Oval Drive, West Lafayette, IN 47907-2084, USA.

    Country: England

    England Research PublicationEngland Research Publication

    AGENCY:

    GRANT:

    ACRONYM:

    MEDLINETA: J Mass Spectrom

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

    Protein identification via ion-trap collision-induced dissociation and examination of low-mass product ions Related Publications

     

    Molecular Station USER Menu

    Welcome to Molecular Station!

    You have to register before you can post on our forums or use our advanced features. Register Now! Its Free and Fast!

    Already registered? Login now below.

    User Name:

    Password:

    Already registered and Forgot your password? Click below to recover it.

    Recover Lost Password

    Join now - it's fast and free!

    Molecular Station is THE largest network of researchers, scientists and science lovers anywhere!

    Research Terms of Usage and Disclaimer
    Home
    Features

    Protocols

    DNA Forum

    Science Forum

    DNA Forum
    Biology Forum

    Science News


    [CaRP] XML error: Invalid document end at line 2

    For more click here:Science News