Literature DB >> 12460775

Expression of CB2 cannabinoid receptor in Pichia pastoris.

Wenke Feng1, Jian Cai, William M Pierce, Zhao-Hui Song.   

Abstract

To facilitate purification and structural characterization, the CB2 cannabinoid receptor is expressed in methylotrophic yeast Pichia pastoris. The expression plasmids were constructed in which the CB2 gene is under the control of the highly inducible promoter of P. pastoris alcohol oxidase 1 gene. A c-myc epitope and a hexahistidine tag were introduced at the C-terminal of the CB2 to permit easy detection and purification. In membrane preparations of CB2 gene transformed yeast cells, Western blot analysis detected the expression of CB2 proteins. Radioligand binding assays demonstrated that the CB2 receptors expressed in P. pastoris have a pharmacological profile similar to that of the receptors expressed in mammalian systems. Furthermore, the epitope-tagged receptor was purified by metal chelating chromatography and the purified CB2 preparations were subjected to digestion by trypsin. MALDI/TOF mass spectrometry analysis of the peptides extracted from tryptic digestions detected 14 peptide fragments derived from the CB2 receptor. ESI mass spectrometry was used to sequence one of these peptide fragments, thus, further confirming the identity of the purified receptor. In conclusion, these data demonstrated for the first time that epitope-tagged, functional CB2 cannabinoid receptor can be expressed in P. pastoris for purification.

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Year:  2002        PMID: 12460775     DOI: 10.1016/s1046-5928(02)00569-7

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


  9 in total

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Authors:  Alexei A Yeliseev; Karen K Wong; Olivier Soubias; Klaus Gawrisch
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2.  Application of HaloTag technology to expression and purification of cannabinoid receptor CB2.

Authors:  Silvia Locatelli-Hoops; Fangmin C Sheen; Lioudmila Zoubak; Klaus Gawrisch; Alexei A Yeliseev
Journal:  Protein Expr Purif       Date:  2013-03-05       Impact factor: 1.650

3.  Progress toward heterologous expression of active G-protein-coupled receptors in Saccharomyces cerevisiae: Linking cellular stress response with translocation and trafficking.

Authors:  Michelle A O'Malley; J Dominic Mancini; Carissa L Young; Emily C McCusker; David Raden; Anne S Robinson
Journal:  Protein Sci       Date:  2009-11       Impact factor: 6.725

4.  High-level expression in Saccharomyces cerevisiae enables isolation and spectroscopic characterization of functional human adenosine A2a receptor.

Authors:  Michelle A O'Malley; Tzvetana Lazarova; Zachary T Britton; Anne S Robinson
Journal:  J Struct Biol       Date:  2007-05-16       Impact factor: 2.867

5.  Efficient digestion and mass spectral analysis of vesicular glutamate transporter 1: a recombinant membrane protein expressed in yeast.

Authors:  Holly D Cox; Chih-Kai Chao; Sarjubhai A Patel; Charles M Thompson
Journal:  J Proteome Res       Date:  2008-01-08       Impact factor: 4.466

6.  Stabilization of functional recombinant cannabinoid receptor CB(2) in detergent micelles and lipid bilayers.

Authors:  Krishna Vukoti; Tomohiro Kimura; Laura Macke; Klaus Gawrisch; Alexei Yeliseev
Journal:  PLoS One       Date:  2012-10-03       Impact factor: 3.240

Review 7.  Methods for recombinant expression and functional characterization of human cannabinoid receptor CB2.

Authors:  Alexei A Yeliseev
Journal:  Comput Struct Biotechnol J       Date:  2013-09-06       Impact factor: 7.271

8.  Recombinant expression of pleurocidin cDNA using the Pichia pastoris expression system.

Authors:  Olive-Jean Burrowes; Gill Diamond; Tung-Ching Lee
Journal:  J Biomed Biotechnol       Date:  2005

9.  Thermostability of a recombinant G protein-coupled receptor expressed at high level in mammalian cell culture.

Authors:  Alexei Yeliseev; Arjen van den Berg; Lioudmila Zoubak; Kirk Hines; Sam Stepnowski; Kyle Williston; Wanhua Yan; Klaus Gawrisch; Jonathan Zmuda
Journal:  Sci Rep       Date:  2020-10-08       Impact factor: 4.996

  9 in total

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