The melanocortin receptors (MCRs) are G-Protein Coupled Receptors (GPCRs) that modulate and control many critical physiological processes in animals including pigmentation, response to stress, feeding behavior, energy balance, sexual function and behavior, inflammatory response, cardiovascular function, immune response, pain and others. They also are involved in many of our most common degenerative diseases including adrenal dysfunction, obesity, anorexia, pigmentary disorders, sexual dysfunction, prolonged and neuropathic pain, inflammatory disorders, cardiovascular disease and others. Yet there are few compounds that have been developed and are pharmaceuticals in use for treatment of these diseases which are our most common and difficult to treat diseases. This grant is dedicated to developing more potent, receptor selective, and specific and most efficacious ligands for the melancortin 1(MCI), melanocortin 3 (MC3), melanocortin 4 (MC4), and melanocortin 5 (MC5) receptors. These novel ligands, which are biological stable and available for in vivo applications, will be useful for studying the pharmacology, physiology and medical applications of melanotropin ligands.
The specific aims we will pursue include: 1) development and use of novel protein/peptide topologies and scaffolds, in conjunction with novel constrained amino acids, to design and synthesize novel orthosteric, allosteric, and biased melanotropin peptides and peptide mimetics with enhanced stability, bioavailability, selectivity and potency for the melanocortin receptors; 2a) to examine binding affinities, cyclic AMP production, efficacies, Ca+2 assays and assays for ?- arrestin. The novel ligands for the hMC1R, hMC3R, hMC4R and hMC5R receptors will be examined with special attention to the development of biased ligands; and 2b) use of novel selective ligands, especially those with biased activity, to explore novel physiological functions that can lead to novel drugs with our collaborators.

Public Health Relevance

The melanotropin peptides and melanocortin receptors are primordial peptides and G-protein coupled receptors that affect many critical biological functions and which are involved in many critical aspects of human health and disease including pigmentary disorders, obesity, prolonged and neuropathic pain, diabetes, cancer, sexual response and motivation, inflammatory response, and many others. We are world leaders in developing selective agonists and antagonists for melanocortin receptors and we will utilize our knowledge and expertise to develop new ligands for these receptors that are more biologically specific and bioavailable so that potential drugs will emerge from these investigations.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM108040-02S1
Application #
9027124
Study Section
Program Officer
Dunsmore, Sarah
Project Start
2014-01-15
Project End
2017-11-30
Budget Start
2014-12-01
Budget End
2015-11-30
Support Year
2
Fiscal Year
2015
Total Cost
$62,185
Indirect Cost
Name
University of Arizona
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
806345617
City
Tucson
State
AZ
Country
United States
Zip Code
85721
Mowlazadeh Haghighi, Saghar; Zhou, Yang; Dai, Jixun et al. (2018) Replacement of Arg with Nle and modified D-Phe in the core sequence of MSHs, Ac-His-D-Phe-Arg-Trp-NH2, leads to hMC1R selectivity and pigmentation. Eur J Med Chem 151:815-823
Durek, Thomas; Cromm, Philipp M; White, Andrew M et al. (2018) Development of Novel Melanocortin Receptor Agonists Based on the Cyclic Peptide Framework of Sunflower Trypsin Inhibitor-1. J Med Chem 61:3674-3684
Merlino, Francesco; Zhou, Yang; Cai, Minying et al. (2018) Development of Macrocyclic Peptidomimetics Containing Constrained ?,?-Dialkylated Amino Acids with Potent and Selective Activity at Human Melanocortin Receptors. J Med Chem 61:4263-4269
Zhou, Yang; Mowlazadeh Haghighi, Saghar; Zoi, Ioanna et al. (2017) Design of MC1R Selective ?-MSH Analogues with Canonical Amino Acids Leads to Potency and Pigmentation. J Med Chem 60:9320-9329
Zhou, Yang; Cai, Minying (2017) Novel approaches to the design of bioavailable melanotropins. Expert Opin Drug Discov 12:1023-1030
Rinne, Petteri; Rami, Martina; Nuutinen, Salla et al. (2017) Melanocortin 1 Receptor Signaling Regulates Cholesterol Transport in Macrophages. Circulation 136:83-97
Cai, Minying; Marelli, Udaya Kiran; Mertz, Blake et al. (2017) Structural Insights into Selective Ligand-Receptor Interactions Leading to Receptor Inactivation Utilizing Selective Melanocortin 3 Receptor Antagonists. Biochemistry 56:4201-4209
Liu, Zhonglin; Gray, Brian D; Barber, Christy et al. (2016) Characterization of TCP-1 probes for molecular imaging of colon cancer. J Control Release 239:223-30
Cai, Minying; Hruby, Victor J (2016) Design of cyclized selective melanotropins. Biopolymers 106:876-883
Hruby, Victor J (2016) Design of cyclic peptides with biological activities from biologically active peptides: the case of peptide modulators of melanocortin receptors. Biopolymers 106:884-888

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