Literature DB >> 19913576

Accelerated digestion for high-throughput proteomics analysis of whole bacterial proteomes.

Ali R Vaezzadeh1, Jacques M P Deshusses, Patrice Waridel, Patrice François, Catherine G Zimmermann-Ivol, Pierre Lescuyer, Jacques Schrenzel, Denis F Hochstrasser.   

Abstract

In bottom-up proteomics, rapid and efficient protein digestion is crucial for data reliability. However, sample preparation remains one of the rate-limiting steps in proteomics workflows. In this study, we compared the conventional trypsin digestion procedure with two accelerated digestion protocols based on shorter reaction times and microwave-assisted digestion for the preparation of membrane-enriched protein fractions of the human pathogenic bacterium Staphylococcus aureus. Produced peptides were analyzed by Shotgun IPG-IEF, a methodology relying on separation of peptides by IPG-IEF before the conventional LC-MS/MS steps of shotgun proteomics. Data obtained on two LC-MS/MS platforms showed that accelerated digestion protocols, especially the one relying on microwave irradiation, enhanced the cleavage specificity of trypsin and thus improved the digestion efficiency especially for hydrophobic and membrane proteins. The combination of high-throughput proteomics with accelerated and efficient sample preparation should enhance the practicability of proteomics by reducing the time from sample collection to obtaining the results. Copyright 2009 Elsevier B.V. All rights reserved.

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Year:  2009        PMID: 19913576     DOI: 10.1016/j.mimet.2009.10.019

Source DB:  PubMed          Journal:  J Microbiol Methods        ISSN: 0167-7012            Impact factor:   2.363


  8 in total

Review 1.  Glycomics and glycoproteomics of membrane proteins and cell-surface receptors: Present trends and future opportunities.

Authors:  Kevin Brown Chandler; Catherine E Costello
Journal:  Electrophoresis       Date:  2016-03-29       Impact factor: 3.535

2.  The GlycoFilter: a simple and comprehensive sample preparation platform for proteomics, N-glycomics and glycosylation site assignment.

Authors:  Hui Zhou; John W Froehlich; Andrew C Briscoe; Richard S Lee
Journal:  Mol Cell Proteomics       Date:  2013-07-02       Impact factor: 5.911

3.  PNGase F catalyzes de-N-glycosylation in a domestic microwave.

Authors:  Hui Zhou; Andrew C Briscoe; John W Froehlich; Richard S Lee
Journal:  Anal Biochem       Date:  2012-04-16       Impact factor: 3.365

4.  Lectin and Liquid Chromatography-Based Methods for Immunoglobulin (G) Glycosylation Analysis.

Authors:  Tea Petrović; Irena Trbojević-Akmačić
Journal:  Exp Suppl       Date:  2021

5.  Universal Solid-Phase Reversible Sample-Prep for Concurrent Proteome and N-Glycome Characterization.

Authors:  Hui Zhou; Samantha Morley; Stephen Kostel; Michael R Freeman; Vivek Joshi; David Brewster; Richard S Lee
Journal:  J Proteome Res       Date:  2016-02-08       Impact factor: 4.466

6.  Evaluation and optimization of mass spectrometric settings during data-dependent acquisition mode: focus on LTQ-Orbitrap mass analyzers.

Authors:  Anastasia Kalli; Geoffrey T Smith; Michael J Sweredoski; Sonja Hess
Journal:  J Proteome Res       Date:  2013-05-31       Impact factor: 4.466

7.  Ctf3/CENP-I provides a docking site for the desumoylase Ulp2 at the kinetochore.

Authors:  Yun Quan; Stephen M Hinshaw; Pang-Che Wang; Stephen C Harrison; Huilin Zhou
Journal:  J Cell Biol       Date:  2021-06-03       Impact factor: 10.539

8.  Can electromagnetic fields influence the structure and enzymatic digest of proteins? A critical evaluation of microwave-assisted proteomics protocols.

Authors:  Markus Damm; Christoph Nusshold; David Cantillo; Gerald N Rechberger; Karl Gruber; Wolfgang Sattler; C Oliver Kappe
Journal:  J Proteomics       Date:  2012-08-06       Impact factor: 4.044

  8 in total

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