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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5988326/ https://www.ncbi.nlm.nih.gov/pubmed/29870551 http://dx.doi.org/10.1371/journal.pone.0198247 |
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author | Kus, Nicole J. Dolinska, Monika B. Young, Kenneth L. Dimitriadis, Emilios K. Wingfield, Paul T. Sergeev, Yuri V. |
author_facet | Kus, Nicole J. Dolinska, Monika B. Young, Kenneth L. Dimitriadis, Emilios K. Wingfield, Paul T. Sergeev, Yuri V. |
author_sort | Kus, Nicole J. |
collection | PubMed |
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, hTyrC(tr) (residues 19–469). Active hTyr is monomeric in detergent micelles suggesting no stable interactions between protein molecules. Both, hTyr and hTyrC(tr), 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. |
format | Online Article Text |
id | pubmed-5988326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-59883262018-06-16 Membrane-associated human tyrosinase is an enzymatically active monomeric glycoprotein Kus, Nicole J. Dolinska, Monika B. Young, Kenneth L. Dimitriadis, Emilios K. Wingfield, Paul T. Sergeev, Yuri V. PLoS One Research Article 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, hTyrC(tr) (residues 19–469). Active hTyr is monomeric in detergent micelles suggesting no stable interactions between protein molecules. Both, hTyr and hTyrC(tr), 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. Public Library of Science 2018-06-05 /pmc/articles/PMC5988326/ /pubmed/29870551 http://dx.doi.org/10.1371/journal.pone.0198247 Text en https://creativecommons.org/publicdomain/zero/1.0/ 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. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication. |
spellingShingle | Research Article Kus, Nicole J. Dolinska, Monika B. Young, Kenneth L. Dimitriadis, Emilios K. Wingfield, Paul T. Sergeev, Yuri V. Membrane-associated human tyrosinase is an enzymatically active monomeric glycoprotein |
title | Membrane-associated human tyrosinase is an enzymatically active monomeric glycoprotein |
title_full | Membrane-associated human tyrosinase is an enzymatically active monomeric glycoprotein |
title_fullStr | Membrane-associated human tyrosinase is an enzymatically active monomeric glycoprotein |
title_full_unstemmed | Membrane-associated human tyrosinase is an enzymatically active monomeric glycoprotein |
title_short | Membrane-associated human tyrosinase is an enzymatically active monomeric glycoprotein |
title_sort | membrane-associated human tyrosinase is an enzymatically active monomeric glycoprotein |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5988326/ https://www.ncbi.nlm.nih.gov/pubmed/29870551 http://dx.doi.org/10.1371/journal.pone.0198247 |
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