Overexpression and functional characterisation of the human melanocortin 4 receptor in Sf9 cells

被引:9
作者
Dolby, V
Collen, A
Lundqvist, A
Cronet, P [1 ]
机构
[1] AstraZeneca R&D, Mol Sci, S-43183 Molndal, Sweden
[2] Lund Univ, Ctr Chem & Chem Engn, Dept Biochem, S-22100 Lund, Sweden
关键词
melanocortin receptor 4; GPCR; overproduction; insect cells; functional characterisation; membrane protein;
D O I
10.1016/j.pep.2004.06.018
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The human melanocortin 4 receptor (MC4r) was successfully expressed in Sf9 cells using the baculovirus infection system. N- and C-terminally His-tagged receptors generated B-max values of 14 and 23 pmol receptor/mg membrane protein, respectively. The highest expression level obtained with the C-terminally His-tagged MC4r corresponded to 0.25 mg active receptor/litre culture volume. Addition of a viral signal peptide at the N-terminus of the His-tagged MC4r did not improve the expression level. Confocal laser microscopy studies revealed that both the N- and C-terminally tagged MC4r did not accumulate intracellularly and were mainly located in the plasma membrane. The recombinant receptors showed similar affinity for the agonist NDP-MSH (K-d = 11 nM) as to MC4r expressed in mammalian cells. Functional coupling of the highest expressed C-terminal tagged receptor to endogenous Galpha protein was demonstrated through 6TPgammaS binding upon agonist stimulation of the receptor. K-i values for the ligands MTII, HS014, alpha-, beta-, and gamma-MSH are comparable to the values obtained for MC4r expressed in mammalian cells. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:455 / 461
页数:7
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