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Gewählte Publikation:

Einhauer, A; Jungbauer, A; .
(2001): The FLAG peptide, a versatile fusion tag for the purification of recombinant proteins.
J Biochem Biophys Methods. 2001; 49(1-3):455-465

Abstract:
A fusion tag, called FLAG (TM) 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 (TM) peptide. Antibodies M2 and M5 are applied in this procedure. Examples demonstrating the versatility, practicability and limitations of this technology are given. (C) 2001 Elsevier Science BN. All rights reserved.
Autor*innen der BOKU Wien:
Jungbauer Alois
BOKU Gendermonitor:

Find related publications in this database (using NML MeSH Indexing)
Antibodies/chemistry;Antibodies/isolation & purification;Binding Sites;Carrier Proteins/isolation & purification;Chromatography, Affinity/methods;Enzymes/isolation & purification;Epitopes/chemistry;Oligopeptides;Peptides/chemistry*;Peptides/immunology;Peptides/isolation & purification;Recombinant Fusion Proteins/isolation & purification;Recombinant Proteins/isolation & purification*;

Find related publications in this database (Keywords)
chromatography
FLAG (TM)
recombinant proteins


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