Difference between revisions of "PMID:15253427"

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'''Zeghouf, M, Li, J, Butland, G, Borkowska, A, Canadien, V, Richards, D, Beattie, B, Emili, A and Greenblatt, JF''' Sequential Peptide Affinity (SPA) system for the identification of mammalian and bacterial protein complexes. ''J. Proteome Res.'' '''3''':463-8
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!align=left align='left' bgcolor='#CCCCFF' |Abstract
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A vector system is described that combines reliable, very low level, regulated protein expression in human cells with two affinity purification tags (Sequential Peptide Affinity, or SPA, system). By avoiding overproduction of the target protein, this system allows for the efficient purification of natural protein complexes and their identification by mass spectrometry. We also present an adaptation of the SPA system for the efficient purification and identification of protein complexes in E. coli and, potentially, other bacteria.
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[http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=pubmed&dopt=Abstract&list_uids=15253427 PubMed]
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!align=left align='left' bgcolor='#CCCCFF' |Keywords
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Cells, Cultured; Electrophoresis, Polyacrylamide Gel; Escherichia coli/genetics; Fluorescent Antibody Technique; Humans; Mass Spectrometry; Multiprotein Complexes/genetics; Multiprotein Complexes/isolation & purification; Multiprotein Complexes/metabolism; Plasmids/genetics; Promoter Regions, Genetic/genetics; Protein Binding/physiology; Recombinant Proteins/genetics; Recombinant Proteins/isolation & purification; Recombinant Proteins/metabolism; Transcription Factors, TFII/genetics; Transcription Factors, TFII/isolation & purification; Transcription Factors, TFII/metabolism
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==Main Points of the Paper ==
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== Materials and Methods Used ==
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==Phenotype Annotations==
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!|Phenotype of!!Taxon Information!!Genotype Information (if known)!!Condition Information!!OMP ID!!OMP Term Name!!ECO ID!!ECO Term Name!!Notes!!Status
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==Notes==
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==References==
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[[Category:Publication]]

Latest revision as of 03:34, 21 September 2018

Citation

Zeghouf, M, Li, J, Butland, G, Borkowska, A, Canadien, V, Richards, D, Beattie, B, Emili, A and Greenblatt, JF Sequential Peptide Affinity (SPA) system for the identification of mammalian and bacterial protein complexes. J. Proteome Res. 3:463-8

Abstract

A vector system is described that combines reliable, very low level, regulated protein expression in human cells with two affinity purification tags (Sequential Peptide Affinity, or SPA, system). By avoiding overproduction of the target protein, this system allows for the efficient purification of natural protein complexes and their identification by mass spectrometry. We also present an adaptation of the SPA system for the efficient purification and identification of protein complexes in E. coli and, potentially, other bacteria.

Links

PubMed

Keywords

Cells, Cultured; Electrophoresis, Polyacrylamide Gel; Escherichia coli/genetics; Fluorescent Antibody Technique; Humans; Mass Spectrometry; Multiprotein Complexes/genetics; Multiprotein Complexes/isolation & purification; Multiprotein Complexes/metabolism; Plasmids/genetics; Promoter Regions, Genetic/genetics; Protein Binding/physiology; Recombinant Proteins/genetics; Recombinant Proteins/isolation & purification; Recombinant Proteins/metabolism; Transcription Factors, TFII/genetics; Transcription Factors, TFII/isolation & purification; Transcription Factors, TFII/metabolism

Main Points of the Paper

Please summarize the main points of the paper.

Materials and Methods Used

Please list the materials and methods used in this paper (strains, plasmids, antibodies, etc).

Phenotype Annotations

See Help:AnnotationTable for details on how to edit this table.
<protect>

Phenotype of Taxon Information Genotype Information (if known) Condition Information OMP ID OMP Term Name ECO ID ECO Term Name Notes Status

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Notes

References

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