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Membrane preconcentration-capillary electrophoresis tandem mass spectrometry (mPC-CE-MS/MS) in the sequence analysis of biologically derived peptides.
Talanta. 1998 Feb; 45(4):603-12.T

Abstract

We demonstrate the use of membrane preconcentration capillary electrophoresis tandem mass spectrometry (mPC-CE-MS/MS) for sequencing peptides at the sub-100 femtomole level. In particular by loading the mPC-CE cartridge off-line with a pressurized bomb apparatus, 100 mul solutions can be loaded in <5 min. Furthermore, mPC-CE-MS in conjunction with on-line transient isotachophoresis carried out in 25 mum i.d. capillaries results in enhanced resolution and theoretical plate values as compared to convention 50-75 mum i.d. capillaries. We show that this is a powerful new approach in the sequencing of biologically derived compounds from complex mixtures such as MHC class I peptides.

Authors+Show Affiliations

Biomedical Mass Spectrometry Facility and Department of Biochemistry and Molecular Biology, Guggenheim CL C009B, Mayo Clinic/Foundation, Rochester, MN 55905, USA; Department of Pharmacology and Clinical Pharmacology Unit, Guggenheim CL C009B, Mayo Clinic/Foundation, Rochester, MN 55905, USA.No affiliation info available

Pub Type(s)

Journal Article

Language

eng

PubMed ID

18967042

Citation

Naylor, S, and A J. Tomlinson. "Membrane Preconcentration-capillary Electrophoresis Tandem Mass Spectrometry (mPC-CE-MS/MS) in the Sequence Analysis of Biologically Derived Peptides." Talanta, vol. 45, no. 4, 1998, pp. 603-12.
Naylor S, Tomlinson AJ. Membrane preconcentration-capillary electrophoresis tandem mass spectrometry (mPC-CE-MS/MS) in the sequence analysis of biologically derived peptides. Talanta. 1998;45(4):603-12.
Naylor, S., & Tomlinson, A. J. (1998). Membrane preconcentration-capillary electrophoresis tandem mass spectrometry (mPC-CE-MS/MS) in the sequence analysis of biologically derived peptides. Talanta, 45(4), 603-12.
Naylor S, Tomlinson AJ. Membrane Preconcentration-capillary Electrophoresis Tandem Mass Spectrometry (mPC-CE-MS/MS) in the Sequence Analysis of Biologically Derived Peptides. Talanta. 1998;45(4):603-12. PubMed PMID: 18967042.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Membrane preconcentration-capillary electrophoresis tandem mass spectrometry (mPC-CE-MS/MS) in the sequence analysis of biologically derived peptides. AU - Naylor,S, AU - Tomlinson,A J, PY - 1997/02/05/received PY - 1997/06/02/revised PY - 1997/06/04/accepted PY - 2008/10/31/pubmed PY - 2008/10/31/medline PY - 2008/10/31/entrez SP - 603 EP - 12 JF - Talanta JO - Talanta VL - 45 IS - 4 N2 - We demonstrate the use of membrane preconcentration capillary electrophoresis tandem mass spectrometry (mPC-CE-MS/MS) for sequencing peptides at the sub-100 femtomole level. In particular by loading the mPC-CE cartridge off-line with a pressurized bomb apparatus, 100 mul solutions can be loaded in <5 min. Furthermore, mPC-CE-MS in conjunction with on-line transient isotachophoresis carried out in 25 mum i.d. capillaries results in enhanced resolution and theoretical plate values as compared to convention 50-75 mum i.d. capillaries. We show that this is a powerful new approach in the sequencing of biologically derived compounds from complex mixtures such as MHC class I peptides. SN - 0039-9140 UR - https://www.unboundmedicine.com/medline/citation/18967042/Membrane_preconcentration_capillary_electrophoresis_tandem_mass_spectrometry__mPC_CE_MS/MS__in_the_sequence_analysis_of_biologically_derived_peptides_ DB - PRIME DP - Unbound Medicine ER -
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