Literature DB >> 18672890

High-speed and high-resolution UPLC separation at zero degrees Celsius.

Thomas E Wales1, Keith E Fadgen, Geoff C Gerhardt, John R Engen.   

Abstract

The conformational properties of proteins can be probed with hydrogen/deuterium exchange mass spectrometry (HXMS). In order to maintain the deuterium label during LC/MS analyses, chromatographic separation must be done rapidly (usually in under 8-10 min) and at 0 degrees C. Traditional RP-HPLC with approximately 3-mum particles has shown generally poor chromatographic performance under these conditions and thereby has been prohibitive for HXMS analyses of larger proteins and many protein complexes. Ultraperformance liquid chromatography (UPLC) employs particles smaller than 2 mum in diameter to achieve superior resolution, speed, and sensitivity as compared to HPLC. UPLC has previously been shown to be compatible with the fast separation and low temperature requirements of HXMS. Here we present construction and validation of a custom UPLC system for HXMS. The system is based on the Waters nanoACQUITY platform and contains a Peltier-cooled module that houses the injection and switching valves, online pepsin digestion column, and C-18 analytical separation column. Single proteins in excess of 95 kDa and a four-protein mixture in excess of 250 kDa have been used to validate the performance of this new system. Near-baseline resolution was achieved in 6-min separations at 0 degrees C and displayed a median chromatographic peak width of approximately 2.7 s at half-height. Deuterium recovery was similar to that obtained using a conventional HPLC and ice bath. This new system represents a significant advancement in HXMS technology that is expected to make the technique more accessible and mainstream in the near future.

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Year:  2008        PMID: 18672890      PMCID: PMC2562353          DOI: 10.1021/ac8008862

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  10 in total

Review 1.  Protein analysis by hydrogen exchange mass spectrometry.

Authors:  Andrew N Hoofnagle; Katheryn A Resing; Natalie G Ahn
Journal:  Annu Rev Biophys Biomol Struct       Date:  2003-02-18

Review 2.  Methods to study protein dynamics and folding by mass spectrometry.

Authors:  Stephen J Eyles; Igor A Kaltashov
Journal:  Methods       Date:  2004-09       Impact factor: 3.608

3.  Ultra-performance liquid chromatography coupled to quadrupole-orthogonal time-of-flight mass spectrometry.

Authors:  Robert Plumb; Jose Castro-Perez; Jennifer Granger; Iain Beattie; Karine Joncour; Andrew Wright
Journal:  Rapid Commun Mass Spectrom       Date:  2004       Impact factor: 2.419

4.  Extensive deuterium back-exchange in certain immobilized pepsin columns used for H/D exchange mass spectrometry.

Authors:  Yan Wu; Suma Kaveti; John R Engen
Journal:  Anal Chem       Date:  2006-03-01       Impact factor: 6.986

5.  Ultra performance liquid chromatography (UPLC) further improves hydrogen/deuterium exchange mass spectrometry.

Authors:  Yan Wu; John R Engen; William B Hobbins
Journal:  J Am Soc Mass Spectrom       Date:  2006-01-10       Impact factor: 3.109

6.  A two-stage differential hydrogen deuterium exchange method for the rapid characterization of protein/ligand interactions.

Authors:  Michael J Chalmers; Scott A Busby; Bruce D Pascal; Mark R Southern; Patrick R Griffin
Journal:  J Biomol Tech       Date:  2007-09

7.  Probing protein ligand interactions by automated hydrogen/deuterium exchange mass spectrometry.

Authors:  Michael J Chalmers; Scott A Busby; Bruce D Pascal; Yuanjun He; Christopher L Hendrickson; Alan G Marshall; Patrick R Griffin
Journal:  Anal Chem       Date:  2006-02-15       Impact factor: 6.986

Review 8.  Hydrogen exchange mass spectrometry for the analysis of protein dynamics.

Authors:  Thomas E Wales; John R Engen
Journal:  Mass Spectrom Rev       Date:  2006 Jan-Feb       Impact factor: 10.946

9.  Determination of amide hydrogen exchange by mass spectrometry: a new tool for protein structure elucidation.

Authors:  Z Zhang; D L Smith
Journal:  Protein Sci       Date:  1993-04       Impact factor: 6.725

10.  Hydrogen exchange-mass spectrometry: optimization of digestion conditions.

Authors:  Lintao Wang; Hai Pan; David L Smith
Journal:  Mol Cell Proteomics       Date:  2002-02       Impact factor: 5.911

  10 in total
  154 in total

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Journal:  Mol Cell Proteomics       Date:  2010-10-05       Impact factor: 5.911

2.  Mass spectrometry-based carboxyl footprinting of proteins: method evaluation.

Authors:  Hao Zhang; Jianzhong Wen; Richard Y-C Huang; Robert E Blankenship; Michael L Gross
Journal:  Int J Mass Spectrom       Date:  2012-02-15       Impact factor: 1.986

3.  The inner membrane histidine kinase EnvZ senses osmolality via helix-coil transitions in the cytoplasm.

Authors:  Loo Chien Wang; Leslie K Morgan; Pahan Godakumbura; Linda J Kenney; Ganesh S Anand
Journal:  EMBO J       Date:  2012-04-27       Impact factor: 11.598

4.  An efficient and inexpensive refrigerated LC system for H/D exchange mass spectrometry.

Authors:  Theodore R Keppel; Martin E Jacques; Robert W Young; Kenneth L Ratzlaff; David D Weis
Journal:  J Am Soc Mass Spectrom       Date:  2011-05-15       Impact factor: 3.109

5.  Molecular insight into the conformational dynamics of the Elongin BC complex and its interaction with HIV-1 Vif.

Authors:  Sean R Marcsisin; John R Engen
Journal:  J Mol Biol       Date:  2010-08-20       Impact factor: 5.469

6.  Resolving isotopic fine structure to detect and quantify natural abundance- and hydrogen/deuterium exchange-derived isotopomers.

Authors:  Qian Liu; Michael L Easterling; Jeffrey N Agar
Journal:  Anal Chem       Date:  2013-12-20       Impact factor: 6.986

7.  Multiple proteolytic events in caspase-6 self-activation impact conformations of discrete structural regions.

Authors:  Kevin B Dagbay; Jeanne A Hardy
Journal:  Proc Natl Acad Sci U S A       Date:  2017-09-01       Impact factor: 11.205

Review 8.  Hydrogen-exchange mass spectrometry for the study of intrinsic disorder in proteins.

Authors:  Deepa Balasubramaniam; Elizabeth A Komives
Journal:  Biochim Biophys Acta       Date:  2012-10-22

9.  GroEL/ES chaperonin modulates the mechanism and accelerates the rate of TIM-barrel domain folding.

Authors:  Florian Georgescauld; Kristina Popova; Amit J Gupta; Andreas Bracher; John R Engen; Manajit Hayer-Hartl; F Ulrich Hartl
Journal:  Cell       Date:  2014-05-08       Impact factor: 41.582

10.  Characterization of Aggregation Propensity of a Human Fc-Fusion Protein Therapeutic by Hydrogen/Deuterium Exchange Mass Spectrometry.

Authors:  Richard Y-C Huang; Roxana E Iacob; Stanley R Krystek; Mi Jin; Hui Wei; Li Tao; Tapan K Das; Adrienne A Tymiak; John R Engen; Guodong Chen
Journal:  J Am Soc Mass Spectrom       Date:  2016-08-15       Impact factor: 3.109

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