Capillary electrochromatography/nanoelectrospray mass spectrometry for attomole characterization of peptides

The successful coupling of capillary electrochromatography (CEC) to an ion trap mass spectrometer via a nanoelectrospray interface (nESI) is described. Using a conductively coated tip butted to the end of a CEC column, it was possible to obtain a stable spray without any sheath liquid being employed...

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Veröffentlicht in:Rapid communications in mass spectrometry 2000-01, Vol.14 (16), p.1448-1454
Hauptverfasser: Guc̆ek, Marjan, Gaspari, Marco, Walhagen, Karin, Vreeken, Rob J., Verheij, Elwin R., van der Greef, Jan
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container_end_page 1454
container_issue 16
container_start_page 1448
container_title Rapid communications in mass spectrometry
container_volume 14
creator Guc̆ek, Marjan
Gaspari, Marco
Walhagen, Karin
Vreeken, Rob J.
Verheij, Elwin R.
van der Greef, Jan
description The successful coupling of capillary electrochromatography (CEC) to an ion trap mass spectrometer via a nanoelectrospray interface (nESI) is described. Using a conductively coated tip butted to the end of a CEC column, it was possible to obtain a stable spray without any sheath liquid being employed. Selected small peptides were separated with CEC columns (100 µm i.d./25 cm long) packed with 3 µm Hypersil C8 or C18 bonded silica particles with an eluent composed of ammonium acetate/acetonitrile. Peptide mixtures of desmopressin, peptide A, oxytocin, carbetocin and [Met5]‐enkephalin were detected in the mid‐attomole range, which is the lowest amount analyzed using CEC combined with MS detection. It was also observed that sensitivity can be compromised at higher separation voltages. We demonstrate that CEC/nESI‐MS, at the current stage of development, represents one of the most sensitive systems for peptide analysis.Copyright © 2000 John Wiley & Sons, Ltd.
doi_str_mv 10.1002/1097-0231(20000830)14:16<1448::AID-RCM44>3.0.CO;2-9
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Mass Spectrom</addtitle><description>The successful coupling of capillary electrochromatography (CEC) to an ion trap mass spectrometer via a nanoelectrospray interface (nESI) is described. Using a conductively coated tip butted to the end of a CEC column, it was possible to obtain a stable spray without any sheath liquid being employed. Selected small peptides were separated with CEC columns (100 µm i.d./25 cm long) packed with 3 µm Hypersil C8 or C18 bonded silica particles with an eluent composed of ammonium acetate/acetonitrile. Peptide mixtures of desmopressin, peptide A, oxytocin, carbetocin and [Met5]‐enkephalin were detected in the mid‐attomole range, which is the lowest amount analyzed using CEC combined with MS detection. It was also observed that sensitivity can be compromised at higher separation voltages. 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subjects Amino Acid Sequence
Chromatography - methods
Deamino Arginine Vasopressin - chemistry
Deamino Arginine Vasopressin - isolation & purification
Enkephalin, Methionine - chemistry
Enkephalin, Methionine - isolation & purification
Mass Spectrometry - methods
Oncogene Protein pp60(v-src) - chemistry
Oncogene Protein pp60(v-src) - isolation & purification
Oxytocin - analogs & derivatives
Oxytocin - chemistry
Oxytocin - isolation & purification
Peptide Fragments - chemistry
Peptide Fragments - isolation & purification
Peptides - isolation & purification
Quality Control
Sensitivity and Specificity
title Capillary electrochromatography/nanoelectrospray mass spectrometry for attomole characterization of peptides
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