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Semi-Synthesis of Labeled Proteins for Spectroscopic Applications
Since the introduction of SPPS by Merrifield in the 60s, peptide chemists have considered the possibility of preparing large proteins. The introduction of native chemical ligation in the 90s and then of expressed protein ligation have opened the way to the preparation of synthetic proteins without s...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269674/ https://www.ncbi.nlm.nih.gov/pubmed/23282535 http://dx.doi.org/10.3390/molecules18010440 |
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author | De Rosa, Lucia Russomanno, Anna Romanelli, Alessandra D’Andrea, Luca Domenico |
author_facet | De Rosa, Lucia Russomanno, Anna Romanelli, Alessandra D’Andrea, Luca Domenico |
author_sort | De Rosa, Lucia |
collection | PubMed |
description | Since the introduction of SPPS by Merrifield in the 60s, peptide chemists have considered the possibility of preparing large proteins. The introduction of native chemical ligation in the 90s and then of expressed protein ligation have opened the way to the preparation of synthetic proteins without size limitations. This review focuses on semi-synthetic strategies useful to prepare proteins decorated with spectroscopic probes, like fluorescent labels and stable isotopes, and their biophysical applications. We show that expressed protein ligation, combining the advantages of organic chemistry with the easy and size limitless recombinant protein expression, is an excellent strategy for the chemical synthesis of labeled proteins, enabling a single protein to be functionalized at one or even more distinct positions with different probes. |
format | Online Article Text |
id | pubmed-6269674 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62696742018-12-14 Semi-Synthesis of Labeled Proteins for Spectroscopic Applications De Rosa, Lucia Russomanno, Anna Romanelli, Alessandra D’Andrea, Luca Domenico Molecules Review Since the introduction of SPPS by Merrifield in the 60s, peptide chemists have considered the possibility of preparing large proteins. The introduction of native chemical ligation in the 90s and then of expressed protein ligation have opened the way to the preparation of synthetic proteins without size limitations. This review focuses on semi-synthetic strategies useful to prepare proteins decorated with spectroscopic probes, like fluorescent labels and stable isotopes, and their biophysical applications. We show that expressed protein ligation, combining the advantages of organic chemistry with the easy and size limitless recombinant protein expression, is an excellent strategy for the chemical synthesis of labeled proteins, enabling a single protein to be functionalized at one or even more distinct positions with different probes. MDPI 2013-01-02 /pmc/articles/PMC6269674/ /pubmed/23282535 http://dx.doi.org/10.3390/molecules18010440 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review De Rosa, Lucia Russomanno, Anna Romanelli, Alessandra D’Andrea, Luca Domenico Semi-Synthesis of Labeled Proteins for Spectroscopic Applications |
title | Semi-Synthesis of Labeled Proteins for Spectroscopic Applications |
title_full | Semi-Synthesis of Labeled Proteins for Spectroscopic Applications |
title_fullStr | Semi-Synthesis of Labeled Proteins for Spectroscopic Applications |
title_full_unstemmed | Semi-Synthesis of Labeled Proteins for Spectroscopic Applications |
title_short | Semi-Synthesis of Labeled Proteins for Spectroscopic Applications |
title_sort | semi-synthesis of labeled proteins for spectroscopic applications |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269674/ https://www.ncbi.nlm.nih.gov/pubmed/23282535 http://dx.doi.org/10.3390/molecules18010440 |
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