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The semisynthesis of nucleolar human selenoprotein H

The human selenoprotein H is the only selenocysteine-containing protein that is located in the cell's nucleolus. In vivo studies have suggested that it plays some role in DNA binding, consumption of reactive oxygen species, and may serve as a safeguard against cancers. However, the protein has...

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Autores principales: Dardashti, Rebecca Notis, Laps, Shay, Gichtin, Jacob S., Metanis, Norman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10646972/
https://www.ncbi.nlm.nih.gov/pubmed/38020378
http://dx.doi.org/10.1039/d3sc03059h
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author Dardashti, Rebecca Notis
Laps, Shay
Gichtin, Jacob S.
Metanis, Norman
author_facet Dardashti, Rebecca Notis
Laps, Shay
Gichtin, Jacob S.
Metanis, Norman
author_sort Dardashti, Rebecca Notis
collection PubMed
description The human selenoprotein H is the only selenocysteine-containing protein that is located in the cell's nucleolus. In vivo studies have suggested that it plays some role in DNA binding, consumption of reactive oxygen species, and may serve as a safeguard against cancers. However, the protein has never been isolated and, as a result, not yet fully characterized. Here, we used a semi-synthetic approach to obtain the full selenoprotein H with a S43T mutation. Using biolayer interferometry, we also show that the Cys-containing mutant of selenoprotein H is capable of binding DNA with sub-micromolar affinity. Employing state-of-the-art expressed protein ligation (EPL), our devised semi-synthetic approach can be utilized for the production of numerous, hard-to-obtain proteins of biological and therapeutic relevance.
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spelling pubmed-106469722023-10-24 The semisynthesis of nucleolar human selenoprotein H Dardashti, Rebecca Notis Laps, Shay Gichtin, Jacob S. Metanis, Norman Chem Sci Chemistry The human selenoprotein H is the only selenocysteine-containing protein that is located in the cell's nucleolus. In vivo studies have suggested that it plays some role in DNA binding, consumption of reactive oxygen species, and may serve as a safeguard against cancers. However, the protein has never been isolated and, as a result, not yet fully characterized. Here, we used a semi-synthetic approach to obtain the full selenoprotein H with a S43T mutation. Using biolayer interferometry, we also show that the Cys-containing mutant of selenoprotein H is capable of binding DNA with sub-micromolar affinity. Employing state-of-the-art expressed protein ligation (EPL), our devised semi-synthetic approach can be utilized for the production of numerous, hard-to-obtain proteins of biological and therapeutic relevance. The Royal Society of Chemistry 2023-10-24 /pmc/articles/PMC10646972/ /pubmed/38020378 http://dx.doi.org/10.1039/d3sc03059h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Dardashti, Rebecca Notis
Laps, Shay
Gichtin, Jacob S.
Metanis, Norman
The semisynthesis of nucleolar human selenoprotein H
title The semisynthesis of nucleolar human selenoprotein H
title_full The semisynthesis of nucleolar human selenoprotein H
title_fullStr The semisynthesis of nucleolar human selenoprotein H
title_full_unstemmed The semisynthesis of nucleolar human selenoprotein H
title_short The semisynthesis of nucleolar human selenoprotein H
title_sort semisynthesis of nucleolar human selenoprotein h
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10646972/
https://www.ncbi.nlm.nih.gov/pubmed/38020378
http://dx.doi.org/10.1039/d3sc03059h
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