Structure⁻Activity Relationships of the Tetrapeptide Ac-His-Arg-( p I)DPhe-Tic-NH 2 at the Mouse Melanocortin Receptors: Modification at the ( p I)DPhe Position Leads to mMC3R Versus mMC4R Selective Ligands
The five melanocortin receptors (MC1R-MC5R) are involved in numerous biological pathways, including steroidogenesis, pigmentation, and food intake. In particular, MC3R and MC4R knockout mice suggest that the MC3R and MC4R regulate energy homeostasis in a non-redundant manner. While MC4R-selective ag...
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Veröffentlicht in: | Molecules (Basel, Switzerland) Switzerland), 2019-04, Vol.24 (8) |
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creator | Schlasner, Katherine N Ericson, Mark D Doering, Skye R Freeman, Katie T Weinrich, Mary Haskell-Luevano, Carrie |
description | The five melanocortin receptors (MC1R-MC5R) are involved in numerous biological pathways, including steroidogenesis, pigmentation, and food intake. In particular, MC3R and MC4R knockout mice suggest that the MC3R and MC4R regulate energy homeostasis in a non-redundant manner. While MC4R-selective agonists have been utilized as appetite modulating agents, the lack of MC3R-selective agonists has impeded progress in modulating this receptor in vivo. In this study, the (
I)DPhe position of the tetrapeptide Ac-His-Arg-(
I)DPhe-Tic-NH
(an MC3R agonist/MC4R antagonist ligand) was investigated with a library of 12 compounds. The compounds in this library were found to have higher agonist efficacy and potency at the mouse (m) MC3R compared to the MC4R, indicating that the Arg-DPhe motif preferentially activates the mMC3R over the mMC4R. This observation may be used in the design of new MC3R-selective ligands, leading to novel probe and therapeutic lead compounds that will be useful for treating metabolic disorders. |
doi_str_mv | 10.3390/molecules24081463 |
format | Article |
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I)DPhe-Tic-NH
(an MC3R agonist/MC4R antagonist ligand) was investigated with a library of 12 compounds. The compounds in this library were found to have higher agonist efficacy and potency at the mouse (m) MC3R compared to the MC4R, indicating that the Arg-DPhe motif preferentially activates the mMC3R over the mMC4R. This observation may be used in the design of new MC3R-selective ligands, leading to novel probe and therapeutic lead compounds that will be useful for treating metabolic disorders.</description><identifier>EISSN: 1420-3049</identifier><identifier>DOI: 10.3390/molecules24081463</identifier><identifier>PMID: 31013889</identifier><language>eng</language><publisher>Switzerland</publisher><ispartof>Molecules (Basel, Switzerland), 2019-04, Vol.24 (8)</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-6783-5972 ; 0000-0002-8715-6010</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,861,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31013889$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schlasner, Katherine N</creatorcontrib><creatorcontrib>Ericson, Mark D</creatorcontrib><creatorcontrib>Doering, Skye R</creatorcontrib><creatorcontrib>Freeman, Katie T</creatorcontrib><creatorcontrib>Weinrich, Mary</creatorcontrib><creatorcontrib>Haskell-Luevano, Carrie</creatorcontrib><title>Structure⁻Activity Relationships of the Tetrapeptide Ac-His-Arg-( p I)DPhe-Tic-NH 2 at the Mouse Melanocortin Receptors: Modification at the ( p I)DPhe Position Leads to mMC3R Versus mMC4R Selective Ligands</title><title>Molecules (Basel, Switzerland)</title><addtitle>Molecules</addtitle><description>The five melanocortin receptors (MC1R-MC5R) are involved in numerous biological pathways, including steroidogenesis, pigmentation, and food intake. In particular, MC3R and MC4R knockout mice suggest that the MC3R and MC4R regulate energy homeostasis in a non-redundant manner. While MC4R-selective agonists have been utilized as appetite modulating agents, the lack of MC3R-selective agonists has impeded progress in modulating this receptor in vivo. In this study, the (
I)DPhe position of the tetrapeptide Ac-His-Arg-(
I)DPhe-Tic-NH
(an MC3R agonist/MC4R antagonist ligand) was investigated with a library of 12 compounds. The compounds in this library were found to have higher agonist efficacy and potency at the mouse (m) MC3R compared to the MC4R, indicating that the Arg-DPhe motif preferentially activates the mMC3R over the mMC4R. This observation may be used in the design of new MC3R-selective ligands, leading to novel probe and therapeutic lead compounds that will be useful for treating metabolic disorders.</description><issn>1420-3049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkM1KAzEQx4Mgtn48gBeZox6iyWaV1lupygqtlLZ4LTE7243sbpZMVujR5_IlfAafxFgsHr3MMPzn_5sPxk6luFRqKK5qV6HpKqQkFQOZ3qg91pdpIrgS6bDHDolehUhkKq8PWE9JIdVgMOyzz0XwnQmdx6_3j5EJ9s2GDcyx0sG6hkrbErgCQomwxOB1i22wOcLI8MwSH_k1P4cWHi_uZiXypTX8KYMEdNhapq6jGCOtccb5YJuINhHhPN1GNbeFNdtJO8cfDGaO7FaaoM4JgoN6OlZzeEZPHf0U6RwWGM-OWyNM7Fo3OR2z_UJXhCe_-YidPdwvxxlvu5ca81Xrba39ZrV7gfq34Rsi0G-A</recordid><startdate>20190413</startdate><enddate>20190413</enddate><creator>Schlasner, Katherine N</creator><creator>Ericson, Mark D</creator><creator>Doering, Skye R</creator><creator>Freeman, Katie T</creator><creator>Weinrich, Mary</creator><creator>Haskell-Luevano, Carrie</creator><scope>NPM</scope><orcidid>https://orcid.org/0000-0002-6783-5972</orcidid><orcidid>https://orcid.org/0000-0002-8715-6010</orcidid></search><sort><creationdate>20190413</creationdate><title>Structure⁻Activity Relationships of the Tetrapeptide Ac-His-Arg-( p I)DPhe-Tic-NH 2 at the Mouse Melanocortin Receptors: Modification at the ( p I)DPhe Position Leads to mMC3R Versus mMC4R Selective Ligands</title><author>Schlasner, Katherine N ; Ericson, Mark D ; Doering, Skye R ; Freeman, Katie T ; Weinrich, Mary ; Haskell-Luevano, Carrie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmed_primary_310138893</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schlasner, Katherine N</creatorcontrib><creatorcontrib>Ericson, Mark D</creatorcontrib><creatorcontrib>Doering, Skye R</creatorcontrib><creatorcontrib>Freeman, Katie T</creatorcontrib><creatorcontrib>Weinrich, Mary</creatorcontrib><creatorcontrib>Haskell-Luevano, Carrie</creatorcontrib><collection>PubMed</collection><jtitle>Molecules (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schlasner, Katherine N</au><au>Ericson, Mark D</au><au>Doering, Skye R</au><au>Freeman, Katie T</au><au>Weinrich, Mary</au><au>Haskell-Luevano, Carrie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structure⁻Activity Relationships of the Tetrapeptide Ac-His-Arg-( p I)DPhe-Tic-NH 2 at the Mouse Melanocortin Receptors: Modification at the ( p I)DPhe Position Leads to mMC3R Versus mMC4R Selective Ligands</atitle><jtitle>Molecules (Basel, Switzerland)</jtitle><addtitle>Molecules</addtitle><date>2019-04-13</date><risdate>2019</risdate><volume>24</volume><issue>8</issue><eissn>1420-3049</eissn><abstract>The five melanocortin receptors (MC1R-MC5R) are involved in numerous biological pathways, including steroidogenesis, pigmentation, and food intake. In particular, MC3R and MC4R knockout mice suggest that the MC3R and MC4R regulate energy homeostasis in a non-redundant manner. While MC4R-selective agonists have been utilized as appetite modulating agents, the lack of MC3R-selective agonists has impeded progress in modulating this receptor in vivo. In this study, the (
I)DPhe position of the tetrapeptide Ac-His-Arg-(
I)DPhe-Tic-NH
(an MC3R agonist/MC4R antagonist ligand) was investigated with a library of 12 compounds. The compounds in this library were found to have higher agonist efficacy and potency at the mouse (m) MC3R compared to the MC4R, indicating that the Arg-DPhe motif preferentially activates the mMC3R over the mMC4R. This observation may be used in the design of new MC3R-selective ligands, leading to novel probe and therapeutic lead compounds that will be useful for treating metabolic disorders.</abstract><cop>Switzerland</cop><pmid>31013889</pmid><doi>10.3390/molecules24081463</doi><orcidid>https://orcid.org/0000-0002-6783-5972</orcidid><orcidid>https://orcid.org/0000-0002-8715-6010</orcidid></addata></record> |
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source | DOAJ Directory of Open Access Journals; MDPI - Multidisciplinary Digital Publishing Institute; EZB-FREE-00999 freely available EZB journals; PubMed Central; Free Full-Text Journals in Chemistry |
title | Structure⁻Activity Relationships of the Tetrapeptide Ac-His-Arg-( p I)DPhe-Tic-NH 2 at the Mouse Melanocortin Receptors: Modification at the ( p I)DPhe Position Leads to mMC3R Versus mMC4R Selective Ligands |
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