2-DIMENSIONAL GEL-ELECTROPHORESIS LIQUID-CHROMATOGRAPHY FOR THE MICROPREPARATIVE ISOLATION OF PROTEINS

被引:27
作者
ROSE, DJ
OPITECK, GJ
机构
[1] Department of Bioanalytical and Structural Chemistry, Glaxo, Inc. Research Institute, North Carolina 27709, 5 Moore Drive, Research Triangle Park
关键词
D O I
10.1021/ac00087a018
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Although comprehensive, column-based two-dimensional separation techniques offer enormous resolving power for a complex mixture, they often lack the ability to isolate the separated species for further analysis (e.g., proteins for Edman sequencing). This paper describes a micropreparative two-dimensional separation system for the isolation of proteins from complex mixtures, such as cell lysates. The system is composed of commercially available equipment: continuous-elution tube gel electrophoresis as the first dimension followed by gradient elution, reversed-phase perfusion liquid chromatography as the second dimension with a two-loop sampling valve as the interface between dimensions. The two-dimensional electrophoresis/liquid chromatography system (2D-EP/LC) shows high resolution of proteins since each dimension has orthogonal separation mechanisms (electrophoresis, size/charge; LC, hydrophobicity). Identification of proteins for further analysis is accomplished by superimposing a grid on the computer-generated 3D image.
引用
收藏
页码:2529 / 2536
页数:8
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[41]   IDENTIFICATION OF MACROPHAGE ACTIVATION-ASSOCIATED PROTEINS BY 2-DIMENSIONAL GEL-ELECTROPHORESIS AND MICROSEQUENCING [J].
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[42]   MAMMALIAN MITOCHONDRIAL RIBOSOMES - CHARACTERIZATION OF RIBOSOMAL-PROTEINS BY 2-DIMENSIONAL GEL-ELECTROPHORESIS [J].
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[43]   2-DIMENSIONAL GEL-ELECTROPHORESIS OF PROTEINS IN HEALTHY ROOTS AND CLUBROOTS OF BRASSICA-OLERACEA [J].
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[44]   VISUALIZATION OF PROTEINS AFTER ISOELECTRIC-FOCUSING DURING 2-DIMENSIONAL GEL-ELECTROPHORESIS [J].
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ANALYTICAL BIOCHEMISTRY, 1979, 98 (01) :81-84
[45]   CHANGES IN SYNTHESIS OF SPECIFIC PROTEINS FOLLOWING AXOTOMY - DETECTION WITH 2-DIMENSIONAL GEL-ELECTROPHORESIS [J].
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STONE, GC .
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[46]   SEPARATION OF MAMMALIAN-CELL SURFACE PROTEINS BY A 2-DIMENSIONAL GEL-ELECTROPHORESIS SYSTEM [J].
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[47]   LINKAGE MAPPING OF 6 POLYMORPHIC LYMPHOCYTE PROTEINS DETECTED BY 2-DIMENSIONAL GEL-ELECTROPHORESIS [J].
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OBRIEN, SJ ;
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[49]   ANALYSIS OF IMMUNE-COMPLEXES BY 2-DIMENSIONAL GEL-ELECTROPHORESIS [J].
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ABRUZZO, JL ;
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CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1985, 34 (02) :165-173
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