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Insights into the deselenization of selenocysteine into alanine and serine
The development of native chemical ligation coupled with desulfurization has allowed ligation at several new ligation junctions. However, desulfurization also converts all cysteine residues in the protein sequence into alanine. Deselenization of selenocysteine, in contrast, selectively removes the s...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054048/ https://www.ncbi.nlm.nih.gov/pubmed/30090236 http://dx.doi.org/10.1039/c5sc02528a |
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author | Dery, Shahar Reddy, Post Sai Dery, Linoy Mousa, Reem Dardashti, Rebecca Notis Metanis, Norman |
author_facet | Dery, Shahar Reddy, Post Sai Dery, Linoy Mousa, Reem Dardashti, Rebecca Notis Metanis, Norman |
author_sort | Dery, Shahar |
collection | PubMed |
description | The development of native chemical ligation coupled with desulfurization has allowed ligation at several new ligation junctions. However, desulfurization also converts all cysteine residues in the protein sequence into alanine. Deselenization of selenocysteine, in contrast, selectively removes the selenol group to give alanine in the presence of unprotected cysteines. In this study we shed more light onto the deselenization mechanism of selenocysteine to alanine and provide optimized conditions for the reaction. The deselenization can be accomplished in one minute under anaerobic conditions to give alanine. Under aerobic conditions (oxygen saturation), selenocysteine is converted into serine. |
format | Online Article Text |
id | pubmed-6054048 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-60540482018-08-08 Insights into the deselenization of selenocysteine into alanine and serine Dery, Shahar Reddy, Post Sai Dery, Linoy Mousa, Reem Dardashti, Rebecca Notis Metanis, Norman Chem Sci Chemistry The development of native chemical ligation coupled with desulfurization has allowed ligation at several new ligation junctions. However, desulfurization also converts all cysteine residues in the protein sequence into alanine. Deselenization of selenocysteine, in contrast, selectively removes the selenol group to give alanine in the presence of unprotected cysteines. In this study we shed more light onto the deselenization mechanism of selenocysteine to alanine and provide optimized conditions for the reaction. The deselenization can be accomplished in one minute under anaerobic conditions to give alanine. Under aerobic conditions (oxygen saturation), selenocysteine is converted into serine. Royal Society of Chemistry 2015-11-01 2015-08-06 /pmc/articles/PMC6054048/ /pubmed/30090236 http://dx.doi.org/10.1039/c5sc02528a Text en This journal is © The Royal Society of Chemistry 2015 https://creativecommons.org/licenses/by/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0) |
spellingShingle | Chemistry Dery, Shahar Reddy, Post Sai Dery, Linoy Mousa, Reem Dardashti, Rebecca Notis Metanis, Norman Insights into the deselenization of selenocysteine into alanine and serine |
title | Insights into the deselenization of selenocysteine into alanine and serine
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title_full | Insights into the deselenization of selenocysteine into alanine and serine
|
title_fullStr | Insights into the deselenization of selenocysteine into alanine and serine
|
title_full_unstemmed | Insights into the deselenization of selenocysteine into alanine and serine
|
title_short | Insights into the deselenization of selenocysteine into alanine and serine
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title_sort | insights into the deselenization of selenocysteine into alanine and serine |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6054048/ https://www.ncbi.nlm.nih.gov/pubmed/30090236 http://dx.doi.org/10.1039/c5sc02528a |
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