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

被引：295

作者：

Einhauer, A ^{[1
]}

Jungbauer, A ^{[1
]}

机构：

[1] Univ Agr & Forestry, Inst Appl Microbiol, A-1190 Vienna, Austria

来源：

JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS | 2001年 / 49卷 / 1-3期

关键词：

chromatography; FLAG (TM); recombinant proteins;

D O I：

10.1016/S0165-022X(01)00213-5

中图分类号：

Q5 [生物化学];

学科分类号：

071010 ; 081704 ;

摘要：

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.

引用

页码：455 / 465

页数：11

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