Enzymatic recycling of ascorbic acid from dehydroascorbic acid by glutathione-like peptides in the extracellular loops of aminergic G-protein coupled receptors
The intracellular recycling of ascorbic acid from dehydroascorbic acid by the glutathione–glutathione reductase system has been well‐characterized. We propose that extracellular recycling of ascorbic acid is performed in a similar manner by cysteine‐rich, glutathione‐like regions of the first and se...
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description | The intracellular recycling of ascorbic acid from dehydroascorbic acid by the glutathione–glutathione reductase system has been well‐characterized. We propose that extracellular recycling of ascorbic acid is performed in a similar manner by cysteine‐rich, glutathione‐like regions of the first and second extracellular loops of some aminergic receptors including adrenergic, histaminergic, and dopaminergic receptors. Previous research in our laboratory demonstrated that ascorbic acid binds to these receptors at a site on their first or second extracellular loops, significantly enhancing ligand activity, and apparently recycling hundreds of times their own concentration of ascorbate in an enzymatic fashion. In this study, we have synthesized 25 peptides from the first and second extracellular loops of aminergic and insulin receptors and compared them directly to glutathione for their ability to prevent the oxidation of ascorbate and to regenerate ascorbate from dehydroascorbic acid. Peptide sequences that mimic glutathione in containing a cysteine and a glutamic acid‐like amino acid also mimic glutathione activity in effects and in kinetics. Some (but not all) peptide sequences that contain one or more methionines instead of cysteine can significantly retard the oxidation of ascorbic acid but do not recycle it from dehydroascorbate into ascorbate. Peptides lacking both cysteines and methionines uniformly failed to alter significantly ascorbate or dehydroascorbate oxidation or reduction. We believe that this is the first proof that receptors may carry out both ligand binding and enzymatic activity extracellularly. Our results suggest the existence of a previously unknown extracellular system for recycling ascorbate. Copyright © 2016 John Wiley & Sons, Ltd.
Ascorbic acid (vitamin C) binds to aminergic receptors enhancing their activity. Twenty‐five peptides from the extracellular loops of aminergic receptors were synthesized and compared directly with glutathione for their ability to prevent the oxidation of ascorbate and to regenerate ascorbate from dehydroascorbic acid. Extracellular recycling of ascorbate is comparable with the intracellular glutathione system and carried out by some cysteine‐rich, glutathione‐like regions of the first and second extracellular loops of adrenergic, histaminergic, and dopaminergic, but not insulin, receptors. |
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Ascorbic acid (vitamin C) binds to aminergic receptors enhancing their activity. Twenty‐five peptides from the extracellular loops of aminergic receptors were synthesized and compared directly with glutathione for their ability to prevent the oxidation of ascorbate and to regenerate ascorbate from dehydroascorbic acid. Extracellular recycling of ascorbate is comparable with the intracellular glutathione system and carried out by some cysteine‐rich, glutathione‐like regions of the first and second extracellular loops of adrenergic, histaminergic, and dopaminergic, but not insulin, receptors.</description><identifier>ISSN: 0952-3499</identifier><identifier>EISSN: 1099-1352</identifier><identifier>DOI: 10.1002/jmr.2530</identifier><identifier>PMID: 26749062</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>adrenergic receptor ; antioxidant ; ascorbate recycling ; Ascorbic acid ; Ascorbic Acid - metabolism ; Binding Sites ; Cysteine ; Cysteine - chemistry ; dehydroascorbate ; Dehydroascorbic Acid - metabolism ; dopamine receptor ; extracellular ; Glutathione ; Glutathione - chemistry ; Glutathione - metabolism ; histamine receptor ; Insulin ; Kinetics ; Methionine - chemistry ; Models, Molecular ; Oxidation ; Oxidation-Reduction ; Peptides ; Peptides - chemical synthesis ; Peptides - chemistry ; Peptides - metabolism ; Protein Structure, Secondary ; reactive oxygen species ; Receptors ; Receptors, G-Protein-Coupled - chemistry ; Receptors, G-Protein-Coupled - metabolism ; Recycling</subject><ispartof>Journal of molecular recognition, 2016-07, Vol.29 (7), p.296-302</ispartof><rights>Copyright © 2016 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5230-609c7d8b619c1a0697c5e69df7c1afe761d5ea938c8698e357f59a02346041823</citedby><cites>FETCH-LOGICAL-c5230-609c7d8b619c1a0697c5e69df7c1afe761d5ea938c8698e357f59a02346041823</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjmr.2530$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjmr.2530$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26749062$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Root-Bernstein, Robert</creatorcontrib><creatorcontrib>Fewins, Jenna</creatorcontrib><creatorcontrib>Rhinesmith, Tyler</creatorcontrib><creatorcontrib>Koch, Ariana</creatorcontrib><creatorcontrib>Dillon, Patrick F.</creatorcontrib><title>Enzymatic recycling of ascorbic acid from dehydroascorbic acid by glutathione-like peptides in the extracellular loops of aminergic G-protein coupled receptors</title><title>Journal of molecular recognition</title><addtitle>J. Mol. Recognit</addtitle><description>The intracellular recycling of ascorbic acid from dehydroascorbic acid by the glutathione–glutathione reductase system has been well‐characterized. We propose that extracellular recycling of ascorbic acid is performed in a similar manner by cysteine‐rich, glutathione‐like regions of the first and second extracellular loops of some aminergic receptors including adrenergic, histaminergic, and dopaminergic receptors. Previous research in our laboratory demonstrated that ascorbic acid binds to these receptors at a site on their first or second extracellular loops, significantly enhancing ligand activity, and apparently recycling hundreds of times their own concentration of ascorbate in an enzymatic fashion. In this study, we have synthesized 25 peptides from the first and second extracellular loops of aminergic and insulin receptors and compared them directly to glutathione for their ability to prevent the oxidation of ascorbate and to regenerate ascorbate from dehydroascorbic acid. Peptide sequences that mimic glutathione in containing a cysteine and a glutamic acid‐like amino acid also mimic glutathione activity in effects and in kinetics. Some (but not all) peptide sequences that contain one or more methionines instead of cysteine can significantly retard the oxidation of ascorbic acid but do not recycle it from dehydroascorbate into ascorbate. Peptides lacking both cysteines and methionines uniformly failed to alter significantly ascorbate or dehydroascorbate oxidation or reduction. We believe that this is the first proof that receptors may carry out both ligand binding and enzymatic activity extracellularly. Our results suggest the existence of a previously unknown extracellular system for recycling ascorbate. Copyright © 2016 John Wiley & Sons, Ltd.
Ascorbic acid (vitamin C) binds to aminergic receptors enhancing their activity. Twenty‐five peptides from the extracellular loops of aminergic receptors were synthesized and compared directly with glutathione for their ability to prevent the oxidation of ascorbate and to regenerate ascorbate from dehydroascorbic acid. Extracellular recycling of ascorbate is comparable with the intracellular glutathione system and carried out by some cysteine‐rich, glutathione‐like regions of the first and second extracellular loops of adrenergic, histaminergic, and dopaminergic, but not insulin, receptors.</description><subject>adrenergic receptor</subject><subject>antioxidant</subject><subject>ascorbate recycling</subject><subject>Ascorbic acid</subject><subject>Ascorbic Acid - metabolism</subject><subject>Binding Sites</subject><subject>Cysteine</subject><subject>Cysteine - chemistry</subject><subject>dehydroascorbate</subject><subject>Dehydroascorbic Acid - metabolism</subject><subject>dopamine receptor</subject><subject>extracellular</subject><subject>Glutathione</subject><subject>Glutathione - chemistry</subject><subject>Glutathione - metabolism</subject><subject>histamine receptor</subject><subject>Insulin</subject><subject>Kinetics</subject><subject>Methionine - chemistry</subject><subject>Models, Molecular</subject><subject>Oxidation</subject><subject>Oxidation-Reduction</subject><subject>Peptides</subject><subject>Peptides - chemical synthesis</subject><subject>Peptides - chemistry</subject><subject>Peptides - metabolism</subject><subject>Protein Structure, Secondary</subject><subject>reactive oxygen species</subject><subject>Receptors</subject><subject>Receptors, G-Protein-Coupled - chemistry</subject><subject>Receptors, G-Protein-Coupled - metabolism</subject><subject>Recycling</subject><issn>0952-3499</issn><issn>1099-1352</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkt1qFDEYhgdR7LYKXoEEPPFkajKZ_B1KaVelKki14EnIZr7ZzTYzGZMZ7PRmvFWzdq0oiB6F5Ht48oa8RfGE4GOCcfVi28XjilF8r1gQrFRJKKvuFwusWFXSWqmD4jClLcZ5xvDD4qDiolaYV4vi22l_M3dmdBZFsLP1rl-j0CKTbIirfGqsa1AbQ4ca2MxNDL9PVjNa-2k048aFHkrvrgANMIyugYRcj8YNILgeo7Hg_eRNRD6EIf24onM9xHU2LcshhhEybsM0eGh2WbIkxPSoeNAan-Dxfj0qPp6dXpy8Ks_fL1-fvDwvLasoLjlWVjRyxYmyxGCuhGXAVdOKvG1BcNIwMIpKK7mSQJlomTK4ojXHNZEVPSqe33pzki8TpFF3Lu0ymx7ClHRmWC0lFvI_UCy5rAVX_0aFYpJTquqMPvsD3YYp9vnNO6rGnNSc_BLaGFKK0Oohus7EWROsd1XQuQp6V4WMPt0Lp1UHzR348-8zUN4CX52H-a8i_ebth71wz7s0wvUdb-KV5oIKpi_fLbX6TD5xdnmhz-h3aIfNZA</recordid><startdate>201607</startdate><enddate>201607</enddate><creator>Root-Bernstein, Robert</creator><creator>Fewins, Jenna</creator><creator>Rhinesmith, Tyler</creator><creator>Koch, Ariana</creator><creator>Dillon, Patrick F.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QF</scope><scope>7QO</scope><scope>7QP</scope><scope>7QQ</scope><scope>7SE</scope><scope>7SR</scope><scope>7TA</scope><scope>7TK</scope><scope>7TM</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>H8G</scope><scope>JG9</scope><scope>P64</scope><scope>7X8</scope><scope>7U5</scope><scope>L7M</scope></search><sort><creationdate>201607</creationdate><title>Enzymatic recycling of ascorbic acid from dehydroascorbic acid by glutathione-like peptides in the extracellular loops of aminergic G-protein coupled receptors</title><author>Root-Bernstein, Robert ; Fewins, Jenna ; Rhinesmith, Tyler ; Koch, Ariana ; Dillon, Patrick F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5230-609c7d8b619c1a0697c5e69df7c1afe761d5ea938c8698e357f59a02346041823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>adrenergic receptor</topic><topic>antioxidant</topic><topic>ascorbate recycling</topic><topic>Ascorbic acid</topic><topic>Ascorbic Acid - metabolism</topic><topic>Binding Sites</topic><topic>Cysteine</topic><topic>Cysteine - chemistry</topic><topic>dehydroascorbate</topic><topic>Dehydroascorbic Acid - metabolism</topic><topic>dopamine receptor</topic><topic>extracellular</topic><topic>Glutathione</topic><topic>Glutathione - chemistry</topic><topic>Glutathione - metabolism</topic><topic>histamine receptor</topic><topic>Insulin</topic><topic>Kinetics</topic><topic>Methionine - chemistry</topic><topic>Models, Molecular</topic><topic>Oxidation</topic><topic>Oxidation-Reduction</topic><topic>Peptides</topic><topic>Peptides - chemical synthesis</topic><topic>Peptides - chemistry</topic><topic>Peptides - metabolism</topic><topic>Protein Structure, Secondary</topic><topic>reactive oxygen species</topic><topic>Receptors</topic><topic>Receptors, G-Protein-Coupled - chemistry</topic><topic>Receptors, G-Protein-Coupled - metabolism</topic><topic>Recycling</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Root-Bernstein, Robert</creatorcontrib><creatorcontrib>Fewins, Jenna</creatorcontrib><creatorcontrib>Rhinesmith, Tyler</creatorcontrib><creatorcontrib>Koch, Ariana</creatorcontrib><creatorcontrib>Dillon, Patrick F.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Aluminium Industry Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Ceramic Abstracts</collection><collection>Corrosion Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Materials Business File</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Copper Technical Reference Library</collection><collection>Materials Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of molecular recognition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Root-Bernstein, Robert</au><au>Fewins, Jenna</au><au>Rhinesmith, Tyler</au><au>Koch, Ariana</au><au>Dillon, Patrick F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enzymatic recycling of ascorbic acid from dehydroascorbic acid by glutathione-like peptides in the extracellular loops of aminergic G-protein coupled receptors</atitle><jtitle>Journal of molecular recognition</jtitle><addtitle>J. Mol. Recognit</addtitle><date>2016-07</date><risdate>2016</risdate><volume>29</volume><issue>7</issue><spage>296</spage><epage>302</epage><pages>296-302</pages><issn>0952-3499</issn><eissn>1099-1352</eissn><abstract>The intracellular recycling of ascorbic acid from dehydroascorbic acid by the glutathione–glutathione reductase system has been well‐characterized. We propose that extracellular recycling of ascorbic acid is performed in a similar manner by cysteine‐rich, glutathione‐like regions of the first and second extracellular loops of some aminergic receptors including adrenergic, histaminergic, and dopaminergic receptors. Previous research in our laboratory demonstrated that ascorbic acid binds to these receptors at a site on their first or second extracellular loops, significantly enhancing ligand activity, and apparently recycling hundreds of times their own concentration of ascorbate in an enzymatic fashion. In this study, we have synthesized 25 peptides from the first and second extracellular loops of aminergic and insulin receptors and compared them directly to glutathione for their ability to prevent the oxidation of ascorbate and to regenerate ascorbate from dehydroascorbic acid. Peptide sequences that mimic glutathione in containing a cysteine and a glutamic acid‐like amino acid also mimic glutathione activity in effects and in kinetics. Some (but not all) peptide sequences that contain one or more methionines instead of cysteine can significantly retard the oxidation of ascorbic acid but do not recycle it from dehydroascorbate into ascorbate. Peptides lacking both cysteines and methionines uniformly failed to alter significantly ascorbate or dehydroascorbate oxidation or reduction. We believe that this is the first proof that receptors may carry out both ligand binding and enzymatic activity extracellularly. Our results suggest the existence of a previously unknown extracellular system for recycling ascorbate. Copyright © 2016 John Wiley & Sons, Ltd.
Ascorbic acid (vitamin C) binds to aminergic receptors enhancing their activity. Twenty‐five peptides from the extracellular loops of aminergic receptors were synthesized and compared directly with glutathione for their ability to prevent the oxidation of ascorbate and to regenerate ascorbate from dehydroascorbic acid. Extracellular recycling of ascorbate is comparable with the intracellular glutathione system and carried out by some cysteine‐rich, glutathione‐like regions of the first and second extracellular loops of adrenergic, histaminergic, and dopaminergic, but not insulin, receptors.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>26749062</pmid><doi>10.1002/jmr.2530</doi><tpages>7</tpages></addata></record> |
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subjects | adrenergic receptor antioxidant ascorbate recycling Ascorbic acid Ascorbic Acid - metabolism Binding Sites Cysteine Cysteine - chemistry dehydroascorbate Dehydroascorbic Acid - metabolism dopamine receptor extracellular Glutathione Glutathione - chemistry Glutathione - metabolism histamine receptor Insulin Kinetics Methionine - chemistry Models, Molecular Oxidation Oxidation-Reduction Peptides Peptides - chemical synthesis Peptides - chemistry Peptides - metabolism Protein Structure, Secondary reactive oxygen species Receptors Receptors, G-Protein-Coupled - chemistry Receptors, G-Protein-Coupled - metabolism Recycling |
title | Enzymatic recycling of ascorbic acid from dehydroascorbic acid by glutathione-like peptides in the extracellular loops of aminergic G-protein coupled receptors |
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