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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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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. |
format | Online Article Text |
id | pubmed-10646972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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