Literature DB >> 27860397

Comparison of sample preparation techniques for large-scale proteomics.

Miljan Kuljanin1, Dylan Z Dieters-Castator2, David A Hess3, Lynne-Marie Postovit2,4, Gilles A Lajoie1.   

Abstract

Numerous workflows exist for large-scale bottom-up proteomics, many of which achieve exceptional proteome depth. Herein, we evaluated the performance of several commonly used sample preparation techniques for proteomic characterization of HeLa lysates [unfractionated in-solution digests, SDS-PAGE coupled with in-gel digestion, gel-eluted liquid fraction entrapment electrophoresis (GELFrEE) technology, SCX StageTips and high-/low-pH reversed phase fractionation (HpH)]. HpH fractionation was found to be superior in terms of proteome depth (>8400 proteins detected) and fractionation efficiency compared to other techniques. SCX StageTip fractionation required minimal sample handling and was also a substantial improvement over SDS-PAGE separation and GELFrEE technology. Sequence coverage of the HeLa proteome increased to 38% when combining all workflows, however, total proteins detected improved only slightly to 8710. In summary, HpH fractionation and SCX StageTips are robust techniques and highly suited for complex proteome analysis.
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Bottom-up proteomics; Gel-eluted liquid fractionation entrapment electrophoresis (GELFrEE); High pH; SCX StageTip; SDS-PAGE; Technology

Mesh:

Substances:

Year:  2017        PMID: 27860397     DOI: 10.1002/pmic.201600337

Source DB:  PubMed          Journal:  Proteomics        ISSN: 1615-9853            Impact factor:   3.984


  7 in total

1.  Parsing disease-relevant protein modifications from epiphenomena: perspective on the structural basis of SOD1-mediated ALS.

Authors:  N D Schmitt; J N Agar
Journal:  J Mass Spectrom       Date:  2017-07       Impact factor: 1.982

2.  Reversible Click Chemistry Tag for Universal Proteome Sample Preparation for Top-Down and Bottom-Up Analysis.

Authors:  Stephanie Biedka; Brigitte F Schmidt; Nolan M Frey; Sarah M Boothman; Jonathan S Minden; Amber Lee Wilson
Journal:  J Proteome Res       Date:  2021-09-15       Impact factor: 5.370

3.  Proteomic analysis of ubiquitination substrates reveals a CTLH E3 ligase complex-dependent regulation of glycolysis.

Authors:  Matthew E R Maitland; Miljan Kuljanin; Xu Wang; Gilles A Lajoie; Caroline Schild-Poulter
Journal:  FASEB J       Date:  2021-09       Impact factor: 5.834

Review 4.  Characterizing Endogenous Protein Complexes with Biological Mass Spectrometry.

Authors:  Rivkah Rogawski; Michal Sharon
Journal:  Chem Rev       Date:  2021-08-18       Impact factor: 72.087

5.  Ultrafast and Reproducible Proteomics from Small Amounts of Heart Tissue Enabled by Azo and timsTOF Pro.

Authors:  Timothy J Aballo; David S Roberts; Jake A Melby; Kevin M Buck; Kyle A Brown; Ying Ge
Journal:  J Proteome Res       Date:  2021-07-08       Impact factor: 4.466

Review 6.  A Comprehensive Guide for Performing Sample Preparation and Top-Down Protein Analysis.

Authors:  Matthew P Padula; Iain J Berry; Matthew B O Rourke; Benjamin B A Raymond; Jerran Santos; Steven P Djordjevic
Journal:  Proteomes       Date:  2017-04-07

7.  The mammalian CTLH complex is an E3 ubiquitin ligase that targets its subunit muskelin for degradation.

Authors:  Matthew E R Maitland; Gabriel Onea; Christopher A Chiasson; Xu Wang; Jun Ma; Sarah E Moor; Kathryn R Barber; Gilles A Lajoie; Gary S Shaw; Caroline Schild-Poulter
Journal:  Sci Rep       Date:  2019-07-08       Impact factor: 4.379

  7 in total

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