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PMID: 11694294 Published · ppublish English Journal Article Review

The FLAG peptide, a versatile fusion tag for the purification of recombinant proteins.

Journal of biochemical and biophysical methods ·Vol. 49 ·No. 1-3 ·2001-10-30 ·Pages 455-65

Einhauer A, Jungbauer A

Abstract

A fusion tag, called FLAG and consisting of eight amino acids (AspTyrLysAspAspAspAspLys) including an enterokinase-cleavage site, was specifically designed for immunoaffinity chromatography. It allows elution under non-denaturing conditions [Bio/Technology, 6 (1988) 1204]. Several antibodies against this peptide have been developed. One antibody, denoted as M1, binds the peptide in the presence of bivalent metal cations, preferably Ca(+). Elution is effected by chelating agents. Another strategy is competitive elution with excess of free FLAG peptide. Antibodies M2 and M5 are applied in this procedure. Examples demonstrating the versatility, practicability and limitations of this technology are given.

MeSH Terms
Antibodies/chemistry,isolation & purification Binding Sites Carrier Proteins/isolation & purification Chromatography, Affinity/methods Enzymes/isolation & purification Epitopes/chemistry Oligopeptides Peptides/chemistry,immunology,isolation & purification Recombinant Fusion Proteins/isolation & purification Recombinant Proteins/isolation & purification
Chemicals
Antibodies Carrier Proteins Enzymes Epitopes Oligopeptides Peptides Recombinant Fusion Proteins Recombinant Proteins FLAG peptide
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Einhauer A
Institute for Applied Microbiology, University of Agriculture and Forestry, Muthgasse 18, 1190 Vienna, Austria. a.einhauer@iam.boku.ac.at
Jungbauer A
Article Info
Journal
Journal of biochemical and biophysical methods
Abbr.
J Biochem Biophys Methods
ISSN
0165-022X
Published
2001-10-30
Pages
455-65
Language
English
Region
Netherlands
NLM ID
7907378
Subset
IM
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