Solution structure of the transmembrane 2 domain of the human melanocortin-4 receptor in sodium dodecyl sulfate (SDS) micelles and the functional implication of the D90N mutant

Abstract The melanocortin receptors (MCRs) are members of the G protein-coupled receptor (GPCR) 1 superfamily with seven transmembrane (TM) domains. Among them, the melanocortin-4 receptor (MC4R) subtype has been highlighted recently by genetic studies in obese humans. In particular, in a patient with severe early-onset obesity, a novel heterozygous mutation in the MC4R gene was found in an exchange of Asp to Asn in the 90th amino acid residue located in the TM 2 domain (MC4R^D90N). Mutations in the MC4R gene are the most frequent monogenic causes of severe obesity and are described as heterozygous with loss of function. We determine solution structures of the TM 2 domain of MC4R (MC4R^TM2) and compared secondary structure of Asp90 mutant (MC4R^TM2-D90N) in a micelle environment by nuclear magnetic resonance (NMR) spectroscopy. NMR structure shows that MC4R^TM2 forms a long α-helix with a kink at Gly98. Interestingly, the structure of MC4R^TM2-D90N is similar to that of MC4R^TM2 based on data from CD and NMR spectrum. However, the thermal stability and homogeneity of MC4R^D90N is quite different from those of MC4R. The structure from molecular modeling suggests that Asp90^2.50 plays a key role in allosteric sodium ion binding. Our data suggest that the sodium ion interaction of Asp90^2.50 in the allosteric pocket of MC4R is essential to its function, explaining the loss of function of the MC4R^D90N mutant.