Literature DB >> 22187450

Comprehensive analysis of protein modifications by top-down mass spectrometry.

Han Zhang1, Ying Ge.   

Abstract

Mass spectrometry (MS)-based proteomics is playing an increasingly important role in cardiovascular research. Proteomics includes identification and quantification of proteins and the characterization of protein modifications, such as posttranslational modifications and sequence variants. The conventional bottom-up approach, involving proteolytic digestion of proteins into small peptides before MS analysis, is routinely used for protein identification and quantification with high throughput and automation. Nevertheless, it has limitations in the analysis of protein modifications, mainly because of the partial sequence coverage and loss of connections among modifications on disparate portions of a protein. An alternative approach, top-down MS, has emerged as a powerful tool for the analysis of protein modifications. The top-down approach analyzes whole proteins directly, providing a "bird's-eye" view of all existing modifications. Subsequently, each modified protein form can be isolated and fragmented in the mass spectrometer to locate the modification site. The incorporation of the nonergodic dissociation methods, such as electron-capture dissociation (ECD), greatly enhances the top-down capabilities. ECD is especially useful for mapping labile posttranslational modifications that are well preserved during the ECD fragmentation process. Top-down MS with ECD has been successfully applied to cardiovascular research, with the unique advantages in unraveling the molecular complexity, quantifying modified protein forms, complete mapping of modifications with full-sequence coverage, discovering unexpected modifications, identifying and quantifying positional isomers, and determining the order of multiple modifications. Nevertheless, top-down MS still needs to overcome some technical challenges to realize its full potential. Herein, we reviewed the advantages and challenges of the top-down method, with a focus on its application in cardiovascular research.

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Year:  2011        PMID: 22187450      PMCID: PMC3320739          DOI: 10.1161/CIRCGENETICS.110.957829

Source DB:  PubMed          Journal:  Circ Cardiovasc Genet        ISSN: 1942-3268


  88 in total

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Authors:  Fred W McLafferty; Kathrin Breuker; Mi Jin; Xuemei Han; Giuseppe Infusini; Honghai Jiang; Xianglei Kong; Tadhg P Begley
Journal:  FEBS J       Date:  2007-11-16       Impact factor: 5.542

5.  Implementation of electron-transfer dissociation on a hybrid linear ion trap-orbitrap mass spectrometer.

Authors:  Graeme C McAlister; Doug Phanstiel; David M Good; W Travis Berggren; Joshua J Coon
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Review 7.  Proteomics by mass spectrometry: approaches, advances, and applications.

Authors:  John R Yates; Cristian I Ruse; Aleksey Nakorchevsky
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9.  Why does troponin I have so many phosphorylation sites? Fact and fancy.

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10.  Two-dimensional electrophoresis-based characterization of post-translational modifications of mammalian 20S proteasome complexes.

Authors:  Chenggong Zong; Glen W Young; Yueju Wang; Haojie Lu; Ning Deng; Oliver Drews; Peipei Ping
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  63 in total

1.  Phosphorylation, but not alternative splicing or proteolytic degradation, is conserved in human and mouse cardiac troponin T.

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Review 2.  Cardiovascular redox and ox stress proteomics.

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3.  MASH Suite Pro: A Comprehensive Software Tool for Top-Down Proteomics.

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Journal:  Mol Cell Proteomics       Date:  2015-11-23       Impact factor: 5.911

4.  Top-Down Proteomics of Large Proteins up to 223 kDa Enabled by Serial Size Exclusion Chromatography Strategy.

Authors:  Wenxuan Cai; Trisha Tucholski; Bifan Chen; Andrew J Alpert; Sean McIlwain; Takushi Kohmoto; Song Jin; Ying Ge
Journal:  Anal Chem       Date:  2017-05-02       Impact factor: 6.986

5.  Top-down analysis of low mass proteins in exosomes shed by murine myeloid-derived suppressor cells.

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6.  Complete posttranslational modification mapping of pathogenic Neisseria meningitidis pilins requires top-down mass spectrometry.

Authors:  Joseph Gault; Christian Malosse; Silke Machata; Corinne Millien; Isabelle Podglajen; Marie-Cécile Ploy; Catherine E Costello; Guillaume Duménil; Julia Chamot-Rooke
Journal:  Proteomics       Date:  2014-03-12       Impact factor: 3.984

7.  Optimizing High-Resolution Mass Spectrometry for the Identification of Low-Abundance Post-Translational Modifications of Intact Proteins.

Authors:  Lisa E Kilpatrick; Eric L Kilpatrick
Journal:  J Proteome Res       Date:  2017-08-08       Impact factor: 4.466

8.  "De-novo" amino acid sequence elucidation of protein G'e by combined "top-down" and "bottom-up" mass spectrometry.

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9.  Top-down targeted proteomics for deep sequencing of tropomyosin isoforms.

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Journal:  J Proteome Res       Date:  2012-12-20       Impact factor: 4.466

Review 10.  Quantitative analysis of global phosphorylation changes with high-resolution tandem mass spectrometry and stable isotopic labeling.

Authors:  Hye Kyong Kweon; Philip C Andrews
Journal:  Methods       Date:  2013-04-21       Impact factor: 3.608

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