Literature DB >> 18461566

Mixed-mode hydrophilic interaction/cation-exchange chromatography: separation of complex mixtures of peptides of varying charge and hydrophobicity.

Colin T Mant1, Robert S Hodges.   

Abstract

Mixed-mode hydrophilic interaction/cation-exchange chromatography (HILIC/CEX) was applied to the separation of two mixtures of synthetic peptide standards: (i) a 27-peptide mixture containing three groups of peptides (each group containing nine peptides of the same net charge of +1, +2 or +3), where the hydrophilicity/hydrophobicity of adjacent peptides within the groups varied only subtly (generally by only a single carbon atom); and (ii) peptide pairs with the same composition but different sequences, where the sole difference between the peptides was the position of a single amino acid substitution. HILIC/CEX is essentially CEX chromatography in the presence of high levels of organic modifier (generally ACN). The present study demonstrated the dramatic effect of increasing ACN concentration (optimum levels of 60-80%, depending on the application) on the separation of both mixtures of peptides. The greater the charge on the peptides, the better the separation achievable by HILIC/CEX. In addition, HILIC/CEX separation of both the peptide mixtures used in the present study was shown to be superior to that of the more commonly applied RP-HPLC mode. Our results highlight again the efficacy of HILIC/CEX as a peptide separation mode in its own right as well as an excellent complement to RP-HPLC.

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Year:  2008        PMID: 18461566      PMCID: PMC2756484          DOI: 10.1002/jssc.200700619

Source DB:  PubMed          Journal:  J Sep Sci        ISSN: 1615-9306            Impact factor:   3.645


  29 in total

1.  Monitoring the hydrophilicity/hydrophobicity of amino acid side-chains in the non-polar and polar faces of amphipathic alpha-helices by reversed-phase and hydrophilic interaction/cation-exchange chromatography.

Authors:  R S Hodges; Y Chen; E Kopecky; C T Mant
Journal:  J Chromatogr A       Date:  2004-10-22       Impact factor: 4.759

2.  The microheterogeneity of the mammalian H1(0) histone. Evidence for an age-dependent deamidation.

Authors:  H Lindner; B Sarg; B Hoertnagl; W Helliger
Journal:  J Biol Chem       Date:  1998-05-22       Impact factor: 5.157

3.  Comparison of the binding of alpha-helical and beta-sheet peptides to a hydrophobic surface.

Authors:  D L Steer; P E Thompson; S E Blondelle; R A Houghten; M I Aguilar
Journal:  J Pept Res       Date:  1998-06

Review 4.  Analysis of synthetic peptides by high-performance liquid chromatography.

Authors:  C T Mant; L H Kondejewski; P J Cachia; O D Monera; R S Hodges
Journal:  Methods Enzymol       Date:  1997       Impact factor: 1.600

5.  Application of hydrophilic-interaction liquid chromatography to the separation of phosphorylated H1 histones.

Authors:  H Lindner; B Sarg; W Helliger
Journal:  J Chromatogr A       Date:  1997-10-03       Impact factor: 4.759

6.  Relationship of sidechain hydrophobicity and alpha-helical propensity on the stability of the single-stranded amphipathic alpha-helix.

Authors:  O D Monera; T J Sereda; N E Zhou; C M Kay; R S Hodges
Journal:  J Pept Sci       Date:  1995 Sep-Oct       Impact factor: 1.905

7.  Hydrophilic interaction/cation-exchange chromatography for the purification of synthetic peptides from closely related impurities: serine side-chain acetylated peptides.

Authors:  J R Litowski; P D Semchuk; C T Mant; R S Hodges
Journal:  J Pept Res       Date:  1999-07

8.  Age-dependent deamidation of H1(0) histones in chromatin of mammalian tissues.

Authors:  H Lindner; B Sarg; H Grunicke; W Helliger
Journal:  J Cancer Res Clin Oncol       Date:  1999       Impact factor: 4.553

9.  Use of sodium perchlorate at low pH for peptide separations by reversed-phase liquid chromatography. Influence of perchlorate ion on apparent hydrophilicity of positively charged amino acid side-chains.

Authors:  T J Sereda; C T Mant; R S Hodges
Journal:  J Chromatogr A       Date:  1997-07-25       Impact factor: 4.759

10.  Induction of amphipathic helical peptide structures in RP-HPLC.

Authors:  A W Purcell; M I Aguilar; R E Wettenhall; M T Hearn
Journal:  Pept Res       Date:  1995 May-Jun
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  3 in total

1.  Design of peptide standards with the same composition and minimal sequence variation to monitor performance/selectivity of reversed-phase matrices.

Authors:  Colin T Mant; Robert S Hodges
Journal:  J Chromatogr A       Date:  2012-01-25       Impact factor: 4.759

Review 2.  Mixed-mode hydrophilic interaction/cation-exchange chromatography (HILIC/CEX) of peptides and proteins.

Authors:  Colin T Mant; Robert S Hodges
Journal:  J Sep Sci       Date:  2008-08       Impact factor: 3.645

3.  An improved approach to hydrophilic interaction chromatography of peptides: salt gradients in the presence of high isocratic acetonitrile concentrations.

Authors:  Colin T Mant; Ziqing Jiang; Barry E Boyes; Robert S Hodges
Journal:  J Chromatogr A       Date:  2013-01-01       Impact factor: 4.759

  3 in total

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