Literature DB >> 34099181

Production and purification of TRPV2 and TRPV5 for structural and functional studies.

Edwin C Fluck1, Ruth A Pumroy2, Vera Y Moiseenkova-Bell3.   

Abstract

The transient receptor potential (TRP) vanilloid 2 (TRPV2) and TRP vanilloid 5 (TRPV5) cation channels play an important role in various physiological and pathophysiological processes. The heterologous expression and purification of these channels is critical for functional and structural characterization of these important proteins. Full-length rat TRPV2 and rabbit TRPV5 can both be expressed in Saccharomyces cerevisiae and affinity purified using the 1D4 epitope and antibody to yield pure, functional channels. Further, these channels can be reconstituted into lipid nanodiscs for a more functionally relevant environment. Presented here are protocols for the expression of full-length rat TRPV2 and rabbit TRPV5 in Saccharomyces cerevisiae, their affinity purification, and their reconstitution into nanodiscs for structural and functional studies.
Copyright © 2021 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  1D4 antibody; Affinity protein purification; Nanodiscs; Saccharomyces cerevisiae protein expression; TRPV2; TRPV5; Transient receptor potential channel

Year:  2021        PMID: 34099181     DOI: 10.1016/bs.mie.2021.02.007

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  1 in total

1.  Structural basis of TRPV5 regulation by physiological and pathophysiological modulators.

Authors:  Edwin C Fluck; Aysenur Torun Yazici; Tibor Rohacs; Vera Y Moiseenkova-Bell
Journal:  Cell Rep       Date:  2022-04-26       Impact factor: 9.995

  1 in total

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