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Overexpression and functional characterisation of the human melanocortin 4 receptor in Sf9 cells
- Source :
- Protein expression and purification. 37(2)
- Publication Year :
- 2004
-
Abstract
- 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. (Less)
- Subjects :
- Insecta
Time Factors
B-cell receptor
Biology
Ligands
Cell Line
Estrogen-related receptor alpha
Enzyme-linked receptor
Animals
Humans
5-HT5A receptor
Receptor
G protein-coupled receptor
DNA Primers
Microscopy, Confocal
Dose-Response Relationship, Drug
Lasers
Molecular biology
Melanocortin 3 receptor
Recombinant Proteins
Protein Structure, Tertiary
Kinetics
Microscopy, Fluorescence
Guanosine 5'-O-(3-Thiotriphosphate)
Receptor, Melanocortin, Type 4
Baculoviridae
Biotechnology
Melanocortin 1 receptor
Protein Binding
Subjects
Details
- ISSN :
- 10465928
- Volume :
- 37
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Protein expression and purification
- Accession number :
- edsair.doi.dedup.....a229b3ff3976869647463910766ae49e