Literature DB >> 26139272

Analysis of Electroblotted Proteins by Mass Spectrometry.

Jose L Luque-Garcia1, Thomas A Neubert.   

Abstract

Identification of proteins by mass spectrometry is crucial for better understanding of many biological, biochemical, and biomedical processes. Here we describe two methods for the identification of electroblotted proteins by on-membrane digestion prior to analysis by mass spectrometry. These on-membrane methods take approximately half the time of in-gel digestion and provide better digestion efficiency, due to the better accessibility of the protease to the proteins adsorbed onto the nitrocellulose, and better protein sequence coverage, especially for membrane proteins where large and hydrophobic peptides are commonly present.

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Year:  2015        PMID: 26139272      PMCID: PMC4501260          DOI: 10.1007/978-1-4939-2718-0_25

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  9 in total

1.  IR-MALDI-mass analysis of electroblotted proteins directly from the membrane: comparison of different membranes, application to on-membrane digestion, and protein identification by database searching.

Authors:  D Schleuder; F Hillenkamp; K Strupat
Journal:  Anal Chem       Date:  1999-08-01       Impact factor: 6.986

2.  Recovery of gel-separated proteins for in-solution digestion and mass spectrometry.

Authors:  A P Jonsson; Y Aissouni; C Palmberg; P Percipalle; E Nordling; B Daneholt; H Jornvall; T Bergman
Journal:  Anal Chem       Date:  2001-11-15       Impact factor: 6.986

3.  Use of nitrocellulose membranes for protein characterization by matrix-assisted laser desorption/ionization mass spectrometry.

Authors:  Jose L Luque-Garcia; Ge Zhou; Tung-Tien Sun; Thomas A Neubert
Journal:  Anal Chem       Date:  2006-07-15       Impact factor: 6.986

4.  Mass spectrometric sequencing of proteins silver-stained polyacrylamide gels.

Authors:  A Shevchenko; M Wilm; O Vorm; M Mann
Journal:  Anal Chem       Date:  1996-03-01       Impact factor: 6.986

5.  Coupling 2D SDS-PAGE with CNBr cleavage and MALDI-TOFMS: a strategy applied to the identification of proteins induced by a hypochlorous acid stress in Escherichia coli.

Authors:  S Dukan; E Turlin; F Biville; G Bolbach; D Touati; J C Tabet; J C Blais
Journal:  Anal Chem       Date:  1998-10-15       Impact factor: 6.986

6.  Characterization of SDS--PAGE-separated proteins by matrix-assisted laser desorption/ionization mass spectrometry.

Authors:  X Liang; J Bai; Y H Liu; D M Lubman
Journal:  Anal Chem       Date:  1996-03-15       Impact factor: 6.986

7.  Colloidal silver staining of electroblotted proteins for high sensitivity peptide mapping by liquid chromatography-electrospray ionization tandem mass spectrometry.

Authors:  I van Oostveen; A Ducret; R Aebersold
Journal:  Anal Biochem       Date:  1997-05-01       Impact factor: 3.365

8.  Proteomic analysis of acrylamide gel separated proteins immobilized on polyvinylidene difluoride membranes following proteolytic digestion in the presence of 80% acetonitrile.

Authors:  Keigo Bunai; Manabu Nozaki; Miyuki Hamano; Shinya Ogane; Taro Inoue; Tadashi Nemoto; Hiroshi Nakanishi; Kunio Yamane
Journal:  Proteomics       Date:  2003-09       Impact factor: 3.984

9.  Efficacy and compatibility with mass spectrometry of methods for elution of proteins from sodium dodecyl sulfate-polyacrylamide gels and polyvinyldifluoride membranes.

Authors:  Charlotte Svaerke Jørgensen; Mitchell Jagd; Birgitte Kjaer Sørensen; Jim McGuire; Vibeke Barkholt; Peter Højrup; Gunnar Houen
Journal:  Anal Biochem       Date:  2004-07-01       Impact factor: 3.365

  9 in total
  1 in total

Review 1.  The biochemical and mass spectrometric profiling of the dystrophin complexome from skeletal muscle.

Authors:  Sandra Murphy; Kay Ohlendieck
Journal:  Comput Struct Biotechnol J       Date:  2015-11-26       Impact factor: 7.271

  1 in total

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