Literature DB >> 3654835

Size-exclusion high-performance liquid chromatography of peptides. Requirement for peptide standards to monitor column performance and non-ideal behaviour.

C T Mant1, J M Parker, R S Hodges.   

Abstract

A series of five synthetic peptide polymers with the sequence Ac-(G-L-G-A-K-G-A-G-V-G)n-amide, where n = 1-5, was employed to assess the resolving power of high-performance size-exclusion columns in peptide separations. The peptide standards showed great versatility in monitoring both ideal (no interactions of solutes with the column material) and non-ideal (hydrophobic and/or ionic interactions of solutes with the column material) size-exclusion behaviour in volatile and non-volatile mobile phases. The effectiveness of adding salts or organic solvents to overcome non-specific interactions of solutes with the column materials was well illustrated by the standards. In addition, the advantageous use of non-ideal size-exclusion behaviour was highlighted. The ability to predict the position and/or elution order of peptides during size-exclusion chromatography (SEC) requires peptides to be separated by a pure size-exclusion process. Although the peptide standards demonstrated similar ideal size-exclusion profiles in non-denaturing medium on all the columns studied, this study suggested that, if the conformational character of a peptide-protein mixture in a particular mobile phase is uncertain and ideal size-exclusion behaviour is required, SEC should be carried out under highly denaturing conditions.

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Year:  1987        PMID: 3654835     DOI: 10.1016/s0021-9673(01)84993-1

Source DB:  PubMed          Journal:  J Chromatogr


  7 in total

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2.  De novo design and structural characterization of an alpha-helical hairpin peptide: a model system for the study of protein folding intermediates.

Authors:  Y Fezoui; D L Weaver; J J Osterhout
Journal:  Proc Natl Acad Sci U S A       Date:  1994-04-26       Impact factor: 11.205

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4.  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

5.  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

6.  HPLC analysis and purification of peptides.

Authors:  Colin T Mant; Yuxin Chen; Zhe Yan; Traian V Popa; James M Kovacs; Janine B Mills; Brian P Tripet; Robert S Hodges
Journal:  Methods Mol Biol       Date:  2007

7.  Size-Exclusion Chromatography for the Analysis of Protein Biotherapeutics and their Aggregates.

Authors:  Paula Hong; Stephan Koza; Edouard S P Bouvier
Journal:  J Liq Chromatogr Relat Technol       Date:  2012-11-30       Impact factor: 1.467

  7 in total

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