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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1988-08-01
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Series: | Journal of Lipid Research |
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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 |
work_keys_str_mv |
AT hujabs highperformanceliquidchromatographyandtimeofflightsecondaryionmassspectrometryanewdimensioninstructuralanalysisofapolipoproteins AT gassmann highperformanceliquidchromatographyandtimeofflightsecondaryionmassspectrometryanewdimensioninstructuralanalysisofapolipoproteins AT dgreifendorf highperformanceliquidchromatographyandtimeofflightsecondaryionmassspectrometryanewdimensioninstructuralanalysisofapolipoproteins AT abenninghoven highperformanceliquidchromatographyandtimeofflightsecondaryionmassspectrometryanewdimensioninstructuralanalysisofapolipoproteins |
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1721510377039069184 |