High performance liquid chromatography and time-of-flight secondary ion mass spectrometry: a new dimension in structural analysis of apolipoproteins.

We report the isolation and characterization of an apolipoprotein A-I mutant using a new technique for structural analysis of apolipoproteins based upon the combined techniques of protein isolation by isoelectric focusing in immobilized pH-gradients, reversed-phase HPLC of tryptic peptides, and subs...

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Main Authors: H U Jabs, G Assmann, D Greifendorf, A Benninghoven
Format: Article
Language:English
Published: Elsevier 1988-08-01
Series:Journal of Lipid Research
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520388064
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spelling doaj-d5edea531e0b46d697f0c7692651730c2021-04-25T04:21:10ZengElsevierJournal of Lipid Research0022-22751988-08-01276613621High performance liquid chromatography and time-of-flight secondary ion mass spectrometry: a new dimension in structural analysis of apolipoproteins.H U JabsG AssmannD GreifendorfA BenninghovenWe report the isolation and characterization of an apolipoprotein A-I mutant using a new technique for structural analysis of apolipoproteins based upon the combined techniques of protein isolation by isoelectric focusing in immobilized pH-gradients, reversed-phase HPLC of tryptic peptides, and subsequent molecular weight analysis of isolated peptides by time-of-flight secondary ion mass spectrometry (TOF-SIMS). The particular advantages of the TOF-SIMS procedure in the characterization of proteolytic peptides are the detection limits in the picomole range, the accuracy of molecular weight determination (up to 3000 +/- 1 D), the speed of analysis, and the wide range of applications for involatile biomolecules. The described procedure for the analysis of apolipoproteins requires only 2 ml of serum as starting material. This method can be used to monitor for genetic polymorphisms and posttranslational modifications on a microscale basis. Applying these techniques, we characterized a new apolipoprotein A-I mutant with an amino acid exchange arginine177 by histidine.http://www.sciencedirect.com/science/article/pii/S0022227520388064
collection DOAJ
language English
format Article
sources DOAJ
author H U Jabs
G Assmann
D Greifendorf
A Benninghoven
spellingShingle H U Jabs
G Assmann
D Greifendorf
A Benninghoven
High performance liquid chromatography and time-of-flight secondary ion mass spectrometry: a new dimension in structural analysis of apolipoproteins.
Journal of Lipid Research
author_facet H U Jabs
G Assmann
D Greifendorf
A Benninghoven
author_sort H U Jabs
title High performance liquid chromatography and time-of-flight secondary ion mass spectrometry: a new dimension in structural analysis of apolipoproteins.
title_short High performance liquid chromatography and time-of-flight secondary ion mass spectrometry: a new dimension in structural analysis of apolipoproteins.
title_full High performance liquid chromatography and time-of-flight secondary ion mass spectrometry: a new dimension in structural analysis of apolipoproteins.
title_fullStr High performance liquid chromatography and time-of-flight secondary ion mass spectrometry: a new dimension in structural analysis of apolipoproteins.
title_full_unstemmed High performance liquid chromatography and time-of-flight secondary ion mass spectrometry: a new dimension in structural analysis of apolipoproteins.
title_sort high performance liquid chromatography and time-of-flight secondary ion mass spectrometry: a new dimension in structural analysis of apolipoproteins.
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 1988-08-01
description We report the isolation and characterization of an apolipoprotein A-I mutant using a new technique for structural analysis of apolipoproteins based upon the combined techniques of protein isolation by isoelectric focusing in immobilized pH-gradients, reversed-phase HPLC of tryptic peptides, and subsequent molecular weight analysis of isolated peptides by time-of-flight secondary ion mass spectrometry (TOF-SIMS). The particular advantages of the TOF-SIMS procedure in the characterization of proteolytic peptides are the detection limits in the picomole range, the accuracy of molecular weight determination (up to 3000 +/- 1 D), the speed of analysis, and the wide range of applications for involatile biomolecules. The described procedure for the analysis of apolipoproteins requires only 2 ml of serum as starting material. This method can be used to monitor for genetic polymorphisms and posttranslational modifications on a microscale basis. Applying these techniques, we characterized a new apolipoprotein A-I mutant with an amino acid exchange arginine177 by histidine.
url http://www.sciencedirect.com/science/article/pii/S0022227520388064
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AT dgreifendorf highperformanceliquidchromatographyandtimeofflightsecondaryionmassspectrometryanewdimensioninstructuralanalysisofapolipoproteins
AT abenninghoven highperformanceliquidchromatographyandtimeofflightsecondaryionmassspectrometryanewdimensioninstructuralanalysisofapolipoproteins
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