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Purification of Recombinant Proteins from Cultured Mammalian Cells by HaloTag Technology.

Authors :
Ohana RF
Hurst R
Source :
Current protocols in molecular biology [Curr Protoc Mol Biol] 2015 Apr 01; Vol. 110, pp. 10.31.1-10.31.15. Date of Electronic Publication: 2015 Apr 01.
Publication Year :
2015

Abstract

Cultured mammalian cells provide an environment ideal for producing functional recombinant mammalian proteins. However, low expression levels of recombinant proteins present a challenge for their detection and purification. This unit will focus on HaloTag, a protein fusion tag designed to bind selectively and covalently to a chloroalkane ligand that may be attached to a variety of functional groups, allowing both protein detection and immobilization. Detection of HaloTag-fusion protein is achieved through binding to a fluorescent chloroalkane ligand, enabling rapid optimization of expression levels. HaloTag-based purification uses covalent capture of the HaloTag fusion onto HaloLink resin coupled with proteolytic cleavage to release the protein of interest from the resin. Covalent binding provides efficient protein capture regardless of expression level and eliminates protein loss during washes of the resin and as a result, offers significant improvements in protein recovery and purity over traditional non-covalent approaches.<br /> (Copyright © 2015 John Wiley & Sons, Inc.)

Details

Language :
English
ISSN :
1934-3647
Volume :
110
Database :
MEDLINE
Journal :
Current protocols in molecular biology
Publication Type :
Academic Journal
Accession number :
25827085
Full Text :
https://doi.org/10.1002/0471142727.mb1031s110