Rapid loading of large sample volumes, analyte cleanup, and modified moving boundary transient isotachophoresis conditions for membrane preconcentration-capillary electrophoresis in small diameter capillaries

被引:46
作者
Tomlinson, AJ
Benson, LM
Jameson, S
Naylor, S
机构
[1] MAYO CLIN,BMSF,DEPT BIOCHEM & MOL BIOL,ROCHESTER,MN 55905
[2] UNIV MINNESOTA,DEPT LAB MED & PATHOL,MINNEAPOLIS,MN 55455
[3] MAYO CLIN,DEPT PHARMACOL,ROCHESTER,MN
[4] MAYO CLIN,CLIN PHARMACOL UNIT,ROCHESTER,MN
关键词
preconcentration; rapid loading; capillary electrophoresis; mass spectrometry; major histocompatibility complex class I peptides;
D O I
10.1002/elps.1150171203
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Using a removable membrane preconcentration (mPC) cartridge, large sample volumes can be loaded prior to final assembly of the mPC capillary electrophoresis (CE) capillary. For narrow-bore (less than or equal to 25 mu m ID) uncoated mPC-CE capillaries, applied to peptide analysis, efficient moving boundary transient isotachphoresis (tITP) conditions at the onset of electrophoresis are described. The enhancement of mPC-CE-mass spectrometry (MS) technology afforded by rapid sample loading and modified moving boundary tITP conditions are demonstrated by analysis of major histocompatibility complex (MHC) class I peptides that were derived from a K-b precipitation of mouse EL-4 cells. Furthermore, we demonstrate the structural characterization of these immunologically significant molecules by mPC-CE-tandem mass spectrometry (mPC-CE-MS/MS).
引用
收藏
页码:1801 / 1807
页数:7
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