Literature DB >> 24480187

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

Yuki Fujii1, Mika Kaneko2, Makiko Neyazaki3, Terukazu Nogi3, Yukinari Kato4, Junichi Takagi5.   

Abstract

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-1, 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.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Immunoaffinity chromatography; Immunodetection; Mammalian cell expression; Monoclonal antibody; Peptide tag; Podoplanin; Purification method

Mesh:

Substances:

Year:  2014        PMID: 24480187     DOI: 10.1016/j.pep.2014.01.009

Source DB:  PubMed          Journal:  Protein Expr Purif        ISSN: 1046-5928            Impact factor:   1.650


  58 in total

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2.  Application of the NZ-1 Fab as a crystallization chaperone for PA tag-inserted target proteins.

Authors:  Risako Tamura; Rika Oi; Satoko Akashi; Mika K Kaneko; Yukinari Kato; Terukazu Nogi
Journal:  Protein Sci       Date:  2019-02-04       Impact factor: 6.725

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Journal:  Endocrinology       Date:  2020-07-01       Impact factor: 4.736

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Authors:  Dawn B Lammert; Frank A Middleton; Jen Pan; Eric C Olson; Brian W Howell
Journal:  J Neurochem       Date:  2017-05-18       Impact factor: 5.372

5.  Redox-assisted regulation of Ca2+ homeostasis in the endoplasmic reticulum by disulfide reductase ERdj5.

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Journal:  Proc Natl Acad Sci U S A       Date:  2016-09-30       Impact factor: 11.205

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Journal:  J Biol Chem       Date:  2020-09-16       Impact factor: 5.157

7.  Structural basis for amyloidogenic peptide recognition by sorLA.

Authors:  Yu Kitago; Masamichi Nagae; Zenzaburo Nakata; Maho Yagi-Utsumi; Shizuka Takagi-Niidome; Emiko Mihara; Terukazu Nogi; Koichi Kato; Junichi Takagi
Journal:  Nat Struct Mol Biol       Date:  2015-02-02       Impact factor: 15.369

8.  Parthenolide Destabilizes Microtubules by Covalently Modifying Tubulin.

Authors:  Takashi Hotta; Sarah E Haynes; Teresa L Blasius; Margo Gebbie; Emily L Eberhardt; David Sept; Michael Cianfrocco; Kristen J Verhey; Alexey I Nesvizhskii; Ryoma Ohi
Journal:  Curr Biol       Date:  2021-01-21       Impact factor: 10.834

9.  Structural insights into integrin α5β1 opening by fibronectin ligand.

Authors:  Stephanie Schumacher; Dirk Dedden; Roberto Vazquez Nunez; Kyoko Matoba; Junichi Takagi; Christian Biertümpfel; Naoko Mizuno
Journal:  Sci Adv       Date:  2021-05-07       Impact factor: 14.136

10.  Lasso-grafting of macrocyclic peptide pharmacophores yields multi-functional proteins.

Authors:  Emiko Mihara; Satoshi Watanabe; Nasir K Bashiruddin; Nozomi Nakamura; Kyoko Matoba; Yumi Sano; Rumit Maini; Yizhen Yin; Katsuya Sakai; Takao Arimori; Kunio Matsumoto; Hiroaki Suga; Junichi Takagi
Journal:  Nat Commun       Date:  2021-03-09       Impact factor: 14.919

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