PA tag: A versatile protein tagging system using a super high affinity antibody against a dodecapeptide derived from human podoplanin

被引:108
作者
Fujii, Yuki [1 ]
Kaneko, Mika [2 ]
Neyazaki, Makiko [3 ]
Nogi, Terukazu [3 ]
Kato, Yukinari [2 ]
Takagi, Junichi [1 ]
机构
[1] Osaka Univ, Inst Prot Res, Lab Prot Synth & Express, Suita, Osaka 5650871, Japan
[2] Tohoku Univ, Grad Sch Med, Dept Reg Innovat, Aoba Ku, Sendai, Miyagi 9808575, Japan
[3] Yokohama City Univ, Grad Sch Med Life Sci, Yokohama, Kanagawa 2300045, Japan
关键词
Purification method; Immunoaffinity chromatography; Monoclonal antibody; Podoplanin; Peptide tag; Immunodetection; Mammalian cell expression; MONOCLONAL-ANTIBODY; RECOMBINANT PROTEINS; PURIFICATION; IDENTIFICATION; GLYCOSYLATION; PEPTIDE;
D O I
10.1016/j.pep.2014.01.009
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Peptide-based epitope tagging technology is universally used in nearly all kind of research projects that involve biochemical characterization of a target protein, but not many systems are fully compatible with purification purpose. By utilizing an anti-human podoplanin antibody NZ-I, we constructed a novel epitope tag system. NZ-1 possesses exceptionally high affinity toward a dodecapeptide dubbed "PA tag", with a characteristic slow dissociation kinetics. Because of its high affinity, PA-tagged proteins in a dilute sample can be captured by immobilized NZ-1 resin in a near complete fashion and eluted by a solution of free PA peptide. This enabled efficient one-step purification of various proteins including soluble (an ectodomain fragment of neuropilin-1) and membrane (epidermal growth factor receptor) proteins expressed in mammalian cells. Mild regeneration condition of the peptide-bound antibody ensures repeated use of the antibody resin, indicating a cost-efficient nature of the system. Together with its outstanding performance in the immunodetection experiments (i.e., Western blotting and flow cytometry), PA tag/NZ-1 system will offer a great chance to facilitate protein production in many biomedical research projects. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:240 / 247
页数:8
相关论文
共 22 条
[1]  
BRIZZARD BL, 1994, BIOTECHNIQUES, V16, P730
[2]   Advances in gentle immunoaffinity chromatography [J].
Burgess, RR ;
Thompson, NE .
CURRENT OPINION IN BIOTECHNOLOGY, 2002, 13 (04) :304-308
[3]   A NOVEL TUMOR-MARKER RELATED TO THE C-MYC ONCOGENE PRODUCT [J].
CHAN, S ;
GABRA, H ;
HILL, F ;
EVAN, G ;
SIKORA, K .
MOLECULAR AND CELLULAR PROBES, 1987, 1 (01) :73-82
[4]   The FLAG™ peptide, a versatile fusion tag for the purification of recombinant proteins [J].
Einhauer, A ;
Jungbauer, A .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 2001, 49 (1-3) :455-465
[5]   ISOLATION OF MONOCLONAL-ANTIBODIES SPECIFIC FOR HUMAN C-MYC PROTO-ONCOGENE PRODUCT [J].
EVAN, GI ;
LEWIS, GK ;
RAMSAY, G ;
BISHOP, JM .
MOLECULAR AND CELLULAR BIOLOGY, 1985, 5 (12) :3610-3616
[6]   PURIFICATION OF A RAS-RESPONSIVE ADENYLYL CYCLASE COMPLEX FROM SACCHAROMYCES-CEREVISIAE BY USE OF AN EPITOPE ADDITION METHOD [J].
FIELD, J ;
NIKAWA, J ;
BROEK, D ;
MACDONALD, B ;
RODGERS, L ;
WILSON, IA ;
LERNER, RA ;
WIGLER, M .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (05) :2159-2165
[7]   GENETIC APPROACH TO FACILITATE PURIFICATION OF RECOMBINANT PROTEINS WITH A NOVEL METAL CHELATE ADSORBENT [J].
HOCHULI, E ;
BANNWARTH, W ;
DOBELI, H ;
GENTZ, R ;
STUBER, D .
BIO-TECHNOLOGY, 1988, 6 (11) :1321-1325
[8]   A SHORT POLYPEPTIDE MARKER SEQUENCE USEFUL FOR RECOMBINANT PROTEIN IDENTIFICATION AND PURIFICATION [J].
HOPP, TP ;
PRICKETT, KS ;
PRICE, VL ;
LIBBY, RT ;
MARCH, CJ ;
CERRETTI, DP ;
URDAL, DL ;
CONLON, PJ .
BIO-TECHNOLOGY, 1988, 6 (10) :1204-1210
[9]   Functional glycosylation of human podoplanin: Glycan structure of platelet aggregation-inducing factor [J].
Kaneko, Mika Kato ;
Kato, Yukinari ;
Kameyama, Akihiko ;
Ito, Hiromi ;
Kuno, Atsushi ;
Hirabayashi, Jun ;
Kubota, Tomomi ;
Amano, Koh ;
Chiba, Yasunori ;
Hasegawa, Yasushi ;
Sasagawa, Isoji ;
Mishima, Kazuhiko ;
Narimatsu, Hisashi .
FEBS LETTERS, 2007, 581 (02) :331-336
[10]   Establishment of a Multi-Specific Monoclonal Antibody MsMab-1 Recognizing Both IDH1 and IDH2 Mutations [J].
Kaneko, Mika Kato ;
Ogasawara, Satoshi ;
Kato, Yukinari .
TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, 2013, 230 (02) :103-109