Membrane-associated human tyrosinase is an enzymatically active monomeric glycoprotein
Human tyrosinase (hTyr) is a Type 1 membrane bound glycoenzyme that catalyzes the initial and rate-limiting steps of melanin production in the melanosome. Mutations in the Tyr gene are linked to oculocutaneous albinism type 1 (OCA1), an autosomal recessive disorder. Currently, the application of enz...
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description | Human tyrosinase (hTyr) is a Type 1 membrane bound glycoenzyme that catalyzes the initial and rate-limiting steps of melanin production in the melanosome. Mutations in the Tyr gene are linked to oculocutaneous albinism type 1 (OCA1), an autosomal recessive disorder. Currently, the application of enzyme replacement therapy for a treatment of OCA1 is hampered by the absence of pure hTyr. Here, full-length hTyr (residues 1-529) was overexpressed in Trichoplusia ni larvae infected with a baculovirus, solubilized with detergent and purified using chromatography. Michaelis-Menten kinetics, enzymatic specific activity, and analytical ultracentrifugation were used to compare the hTyr in detergent with the soluble recombinant intra-melanosomal domain, hTyrCtr (residues 19-469). Active hTyr is monomeric in detergent micelles suggesting no stable interactions between protein molecules. Both, hTyr and hTyrCtr, exhibited similar enzymatic activity and ligand affinity in L-DOPA and L-Tyrosine reactions. In addition, expression in larvae is a scalable process that will allow high yield protein production. Thus, larval production of enzymatically active human tyrosinase potentially could be a useful tool in developing a cure for OCA1. |
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Mutations in the Tyr gene are linked to oculocutaneous albinism type 1 (OCA1), an autosomal recessive disorder. Currently, the application of enzyme replacement therapy for a treatment of OCA1 is hampered by the absence of pure hTyr. Here, full-length hTyr (residues 1-529) was overexpressed in Trichoplusia ni larvae infected with a baculovirus, solubilized with detergent and purified using chromatography. Michaelis-Menten kinetics, enzymatic specific activity, and analytical ultracentrifugation were used to compare the hTyr in detergent with the soluble recombinant intra-melanosomal domain, hTyrCtr (residues 19-469). Active hTyr is monomeric in detergent micelles suggesting no stable interactions between protein molecules. Both, hTyr and hTyrCtr, exhibited similar enzymatic activity and ligand affinity in L-DOPA and L-Tyrosine reactions. In addition, expression in larvae is a scalable process that will allow high yield protein production. Thus, larval production of enzymatically active human tyrosinase potentially could be a useful tool in developing a cure for OCA1.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0198247</identifier><identifier>PMID: 29870551</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Albinism ; Albinism, Oculocutaneous - enzymology ; Albinism, Oculocutaneous - genetics ; Albinism, Oculocutaneous - therapy ; Analysis ; Baculovirus ; Biochemistry ; Biology and Life Sciences ; Care and treatment ; Chromatography ; Dihydroxyphenylalanine ; Disease ; Dopa ; Enzymatic activity ; Enzyme Replacement Therapy ; Enzymes ; Genetic aspects ; Glycoprotein ; Glycoproteins ; Hereditary diseases ; Humans ; Kinetics ; Larvae ; Levodopa ; Medicine and Health Sciences ; Melanin ; Molecular chains ; Molecular weight ; Monophenol Monooxygenase - chemistry ; Monophenol Monooxygenase - genetics ; Monophenol Monooxygenase - therapeutic use ; Mutation ; Oculocutaneous albinism ; Physical Sciences ; Polypeptides ; Protein Domains ; Proteins ; Reaction kinetics ; Recombinant ; Recombinant Proteins - chemistry ; Recombinant Proteins - genetics ; Recombinant Proteins - therapeutic use ; Research and Analysis Methods ; Residues ; Sedimentation & deposition ; Trichoplusia ni ; TYR gene ; Tyrosinase ; Tyrosine ; Ultracentrifugation</subject><ispartof>PloS one, 2018-06, Vol.13 (6), p.e0198247-e0198247</ispartof><rights>COPYRIGHT 2018 Public Library of Science</rights><rights>This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. 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Mutations in the Tyr gene are linked to oculocutaneous albinism type 1 (OCA1), an autosomal recessive disorder. Currently, the application of enzyme replacement therapy for a treatment of OCA1 is hampered by the absence of pure hTyr. Here, full-length hTyr (residues 1-529) was overexpressed in Trichoplusia ni larvae infected with a baculovirus, solubilized with detergent and purified using chromatography. Michaelis-Menten kinetics, enzymatic specific activity, and analytical ultracentrifugation were used to compare the hTyr in detergent with the soluble recombinant intra-melanosomal domain, hTyrCtr (residues 19-469). Active hTyr is monomeric in detergent micelles suggesting no stable interactions between protein molecules. Both, hTyr and hTyrCtr, exhibited similar enzymatic activity and ligand affinity in L-DOPA and L-Tyrosine reactions. In addition, expression in larvae is a scalable process that will allow high yield protein production. Thus, larval production of enzymatically active human tyrosinase potentially could be a useful tool in developing a cure for OCA1.</description><subject>Albinism</subject><subject>Albinism, Oculocutaneous - enzymology</subject><subject>Albinism, Oculocutaneous - genetics</subject><subject>Albinism, Oculocutaneous - therapy</subject><subject>Analysis</subject><subject>Baculovirus</subject><subject>Biochemistry</subject><subject>Biology and Life Sciences</subject><subject>Care and treatment</subject><subject>Chromatography</subject><subject>Dihydroxyphenylalanine</subject><subject>Disease</subject><subject>Dopa</subject><subject>Enzymatic activity</subject><subject>Enzyme Replacement Therapy</subject><subject>Enzymes</subject><subject>Genetic aspects</subject><subject>Glycoprotein</subject><subject>Glycoproteins</subject><subject>Hereditary diseases</subject><subject>Humans</subject><subject>Kinetics</subject><subject>Larvae</subject><subject>Levodopa</subject><subject>Medicine and Health Sciences</subject><subject>Melanin</subject><subject>Molecular chains</subject><subject>Molecular weight</subject><subject>Monophenol Monooxygenase - chemistry</subject><subject>Monophenol Monooxygenase - genetics</subject><subject>Monophenol Monooxygenase - therapeutic use</subject><subject>Mutation</subject><subject>Oculocutaneous albinism</subject><subject>Physical Sciences</subject><subject>Polypeptides</subject><subject>Protein Domains</subject><subject>Proteins</subject><subject>Reaction kinetics</subject><subject>Recombinant</subject><subject>Recombinant Proteins - chemistry</subject><subject>Recombinant Proteins - genetics</subject><subject>Recombinant Proteins - therapeutic use</subject><subject>Research and Analysis Methods</subject><subject>Residues</subject><subject>Sedimentation & deposition</subject><subject>Trichoplusia ni</subject><subject>TYR gene</subject><subject>Tyrosinase</subject><subject>Tyrosine</subject><subject>Ultracentrifugation</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><sourceid>DOA</sourceid><recordid>eNqNkl1rFDEUhgdRbK3-A9EBQfRi1ySTr7kRSvFjoVLwo7chk0l2UzLJNskU119vtrstO9ILycWEM8_7JufkraqXEMxhw-CHqzBGL918HbyeA9hyhNmj6hi2DZpRBJrHB_uj6llKVwCQhlP6tDpCLWeAEHhcXX7TQxel1zOZUlBWZt3Xq3GQvs6bGJL1MunaproUtP-zGWS2Sjq3qaXK9kbXQ_Bh0NGqeuk2KqxjyNr659UTI13SL_bfk-rX508_z77Ozi--LM5Oz2eKtijPTG8MQIbTpscdNwRI0iGikAQGYIKMbJmSAECjWaMQwJwQQg0lDBpMOWbNSfV657t2IYn9SJJAgBQ95C0txGJH9EFeiXW0g4wbEaQVt4UQl0LG0pPTgjJE246WufQIaw056KjGhBEqOW8hKF4f96eN3aB7pX2O0k1Mp3-8XYlluBGk5bxB28u82xvEcD3qlMVgk9LOlQcI4-29IWCYoW1nb_5BH-5uTy1lacB6E8q5amsqTgmGmFHCm0LNH6DK6vVgVcmPsaU-EbyfCAqT9e-8lGNKYvHj-_-zF5dT9u0Bu9LS5VUKbsw2-DQF8Q5UJYMpanM_ZAjENv530xDb-It9_Ivs1eED3Yvu8t78BYTC_04</recordid><startdate>20180605</startdate><enddate>20180605</enddate><creator>Kus, Nicole J</creator><creator>Dolinska, Monika B</creator><creator>Young, 2nd, Kenneth L</creator><creator>Dimitriadis, Emilios K</creator><creator>Wingfield, Paul T</creator><creator>Sergeev, Yuri V</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-7204-6572</orcidid></search><sort><creationdate>20180605</creationdate><title>Membrane-associated human tyrosinase is an enzymatically active monomeric glycoprotein</title><author>Kus, Nicole J ; Dolinska, Monika B ; Young, 2nd, Kenneth L ; Dimitriadis, Emilios K ; Wingfield, Paul T ; Sergeev, Yuri V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-fdff02f863d4b8f50a5b25c2a0f0452fa97ca001fe73c20485556f6571f468473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Albinism</topic><topic>Albinism, Oculocutaneous - enzymology</topic><topic>Albinism, Oculocutaneous - genetics</topic><topic>Albinism, Oculocutaneous - therapy</topic><topic>Analysis</topic><topic>Baculovirus</topic><topic>Biochemistry</topic><topic>Biology and Life Sciences</topic><topic>Care and treatment</topic><topic>Chromatography</topic><topic>Dihydroxyphenylalanine</topic><topic>Disease</topic><topic>Dopa</topic><topic>Enzymatic activity</topic><topic>Enzyme Replacement Therapy</topic><topic>Enzymes</topic><topic>Genetic aspects</topic><topic>Glycoprotein</topic><topic>Glycoproteins</topic><topic>Hereditary diseases</topic><topic>Humans</topic><topic>Kinetics</topic><topic>Larvae</topic><topic>Levodopa</topic><topic>Medicine and Health Sciences</topic><topic>Melanin</topic><topic>Molecular chains</topic><topic>Molecular weight</topic><topic>Monophenol Monooxygenase - chemistry</topic><topic>Monophenol Monooxygenase - genetics</topic><topic>Monophenol Monooxygenase - therapeutic use</topic><topic>Mutation</topic><topic>Oculocutaneous albinism</topic><topic>Physical Sciences</topic><topic>Polypeptides</topic><topic>Protein Domains</topic><topic>Proteins</topic><topic>Reaction kinetics</topic><topic>Recombinant</topic><topic>Recombinant Proteins - chemistry</topic><topic>Recombinant Proteins - genetics</topic><topic>Recombinant Proteins - therapeutic use</topic><topic>Research and Analysis Methods</topic><topic>Residues</topic><topic>Sedimentation & deposition</topic><topic>Trichoplusia ni</topic><topic>TYR gene</topic><topic>Tyrosinase</topic><topic>Tyrosine</topic><topic>Ultracentrifugation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kus, Nicole J</creatorcontrib><creatorcontrib>Dolinska, Monika B</creatorcontrib><creatorcontrib>Young, 2nd, Kenneth L</creatorcontrib><creatorcontrib>Dimitriadis, Emilios K</creatorcontrib><creatorcontrib>Wingfield, Paul T</creatorcontrib><creatorcontrib>Sergeev, Yuri V</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kus, Nicole J</au><au>Dolinska, Monika B</au><au>Young, 2nd, Kenneth L</au><au>Dimitriadis, Emilios K</au><au>Wingfield, Paul T</au><au>Sergeev, Yuri V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Membrane-associated human tyrosinase is an enzymatically active monomeric glycoprotein</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2018-06-05</date><risdate>2018</risdate><volume>13</volume><issue>6</issue><spage>e0198247</spage><epage>e0198247</epage><pages>e0198247-e0198247</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Human tyrosinase (hTyr) is a Type 1 membrane bound glycoenzyme that catalyzes the initial and rate-limiting steps of melanin production in the melanosome. Mutations in the Tyr gene are linked to oculocutaneous albinism type 1 (OCA1), an autosomal recessive disorder. Currently, the application of enzyme replacement therapy for a treatment of OCA1 is hampered by the absence of pure hTyr. Here, full-length hTyr (residues 1-529) was overexpressed in Trichoplusia ni larvae infected with a baculovirus, solubilized with detergent and purified using chromatography. Michaelis-Menten kinetics, enzymatic specific activity, and analytical ultracentrifugation were used to compare the hTyr in detergent with the soluble recombinant intra-melanosomal domain, hTyrCtr (residues 19-469). Active hTyr is monomeric in detergent micelles suggesting no stable interactions between protein molecules. Both, hTyr and hTyrCtr, exhibited similar enzymatic activity and ligand affinity in L-DOPA and L-Tyrosine reactions. In addition, expression in larvae is a scalable process that will allow high yield protein production. Thus, larval production of enzymatically active human tyrosinase potentially could be a useful tool in developing a cure for OCA1.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>29870551</pmid><doi>10.1371/journal.pone.0198247</doi><tpages>e0198247</tpages><orcidid>https://orcid.org/0000-0002-7204-6572</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Albinism Albinism, Oculocutaneous - enzymology Albinism, Oculocutaneous - genetics Albinism, Oculocutaneous - therapy Analysis Baculovirus Biochemistry Biology and Life Sciences Care and treatment Chromatography Dihydroxyphenylalanine Disease Dopa Enzymatic activity Enzyme Replacement Therapy Enzymes Genetic aspects Glycoprotein Glycoproteins Hereditary diseases Humans Kinetics Larvae Levodopa Medicine and Health Sciences Melanin Molecular chains Molecular weight Monophenol Monooxygenase - chemistry Monophenol Monooxygenase - genetics Monophenol Monooxygenase - therapeutic use Mutation Oculocutaneous albinism Physical Sciences Polypeptides Protein Domains Proteins Reaction kinetics Recombinant Recombinant Proteins - chemistry Recombinant Proteins - genetics Recombinant Proteins - therapeutic use Research and Analysis Methods Residues Sedimentation & deposition Trichoplusia ni TYR gene Tyrosinase Tyrosine Ultracentrifugation |
title | Membrane-associated human tyrosinase is an enzymatically active monomeric glycoprotein |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T12%3A49%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Membrane-associated%20human%20tyrosinase%20is%20an%20enzymatically%20active%20monomeric%20glycoprotein&rft.jtitle=PloS%20one&rft.au=Kus,%20Nicole%20J&rft.date=2018-06-05&rft.volume=13&rft.issue=6&rft.spage=e0198247&rft.epage=e0198247&rft.pages=e0198247-e0198247&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0198247&rft_dat=%3Cgale_plos_%3EA541476583%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2050451896&rft_id=info:pmid/29870551&rft_galeid=A541476583&rft_doaj_id=oai_doaj_org_article_67269b6551d24ee180b6e45756a88910&rfr_iscdi=true |