Expression of the human μ opioid receptor in a stable Sf9 cell line

被引:38
|
作者
Kempf, J
Snook, LA
Vonesch, JL
Dahms, TES
Pattus, F
Massotte, D
机构
[1] Ecole Super Biotechnol Strasbourg, CNRS, UPR 9050, Dept Recepteurs & Prot Membranaires, F-67400 Illkirch Graffenstaden, France
[2] Univ Regina, Dept Chem & Biochem, Regina, SK S4S 0A2, Canada
[3] ULP, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire, F-67404 Illkirch Graffenstaden, France
基金
加拿大自然科学与工程研究理事会;
关键词
human mu opioid receptor; G protein-coupled receptor; insect cell; baculovirus expression system; stable expression; OpIE2; promoter;
D O I
10.1016/S0168-1656(02)00008-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The cDNA that encodes the human mu opioid receptor (hMOR) has been cloned and expressed in Spodoptera frugiperda (Sf9) cells using a nonlytic vector system. The coding sequence fused to the cleavable glycoprotein signal peptide gp 64, and a C-terminal histidine tag was placed under the transcriptional control of the Orgyia pseudotsugata multicapsid nucleopolyhedrosis virus immediate-early 2 (OpIE2) promoter. Transfected cells were selected using Zeocin resistance and the receptor was constitutively expressed at approximately 12 000 receptors per cell. Immunofluorescence images illustrated that more than 75% of the Sf9 cells expressed hMOR at the plasma membrane. This is the first report of the constitutive and heterologous expression of a G protein-coupled receptor in a stably transfected Sf9 cell line, under the control of the OpIE2 promoter. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:181 / 187
页数:7
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