D-amino acid scan of gamma-melanocyte-stimulating hormone: Importance of Trp(8) on human MC3 receptor selectivity

In our search;for potent and receptor-selective agonists and antagonists, w e report here the results of D-amino acid substitution at each position of the short peptide gamma -melanocyte-stimulating hormone (gamma -MSH). The n ative gamma -MSH shows weak binding at all three receptors (i.e., the human MC3, MC4, and MC5) and a selectivity of 1-2 orders of magnitude at the MC3 R over the MC4R and MC5R. Sequential replacement of each residue in the gam ma -MSH sequence with the corresponding D-isomer results in analogues which mostly have weaker binding affinity than the native peptide, except for tw o analogues. For the DTrp(8) analogue, there is an increase in binding affi nity by about 1 order of magnitude (IC50 = 6 nM) at the MC3R compared-with that of the natural molecule and an increase in selectivity for the MC3R by 2 orders of magnitude compared with the activity at the MC IR and MC5R. Th e DPhe(6) analogue is about 10-fold more potent (IC50 = 8.8 nM) at the MC3R compared with the native peptide but lacks subtype selectivity. Measuremen t of the intracellular cAMP accumulation in human MC3R, MC4R, and MC5R reve aled that the native peptide shows potent activity at the MC3R (EC50 = 5.9 nM)and is about 50-100-fold selective at this receptor compared with the MC 4R and MC5R. The DArg(10) (EC50 = 35 nM) and DPhe(11) (EC50 = 11 nM) analog ues are selective for the MC3R by 1 and 2 orders of magnitude compared with the MC4R and MC5R, respectively. The DTrp(8) compound (EC50 = 0.33 nM) sho ws about 300- and 250-fold increase in selectivity at the MC3R compared wit h the MC4R and MC5R, respectively. Finally, the DTyr(1) peptide is selectiv e for the MC3R (EC50 = 12 nM) by 40-200-fold compared with the MC4R and MC5 R. In general, the trend is that D-amino acid substitutions of the aromatic residues 1, 6, 8, and 11 and the basic residue Arg(10), but not Arg(7), re sult in an increase in MC3R selectivity over the MC4R and MC5R and only ago nist activity is observed. Thus, the key residues of gamma -MSH identified in this study include the aromatic residues 1, 6, 8, and 11 and the basic r esidue Arg(10) (but not Arg(7)), as important for MC3 selectivity over the MC4 and MC5 subtypes. Further, the study reveals the extreme importance of DTrp at position 8 in imparting potency and selectivity since this is the m ost selective analogue for the human MC3R reported thus far.