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Exploiting Protein N-Terminus for Site-Specific Bioconjugation
Although a plethora of chemistries have been developed to selectively decorate protein molecules, novel strategies continue to be reported with the final aim of improving selectivity and mildness of the reaction conditions, preserve protein integrity, and fulfill all the increasing requirements of t...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8228110/ https://www.ncbi.nlm.nih.gov/pubmed/34207845 http://dx.doi.org/10.3390/molecules26123521 |
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author | De Rosa, Lucia Di Stasi, Rossella Romanelli, Alessandra D’Andrea, Luca Domenico |
author_facet | De Rosa, Lucia Di Stasi, Rossella Romanelli, Alessandra D’Andrea, Luca Domenico |
author_sort | De Rosa, Lucia |
collection | PubMed |
description | Although a plethora of chemistries have been developed to selectively decorate protein molecules, novel strategies continue to be reported with the final aim of improving selectivity and mildness of the reaction conditions, preserve protein integrity, and fulfill all the increasing requirements of the modern applications of protein conjugates. The targeting of the protein N-terminal alpha-amine group appears a convenient solution to the issue, emerging as a useful and unique reactive site universally present in each protein molecule. Herein, we provide an updated overview of the methodologies developed until today to afford the selective modification of proteins through the targeting of the N-terminal alpha-amine. Chemical and enzymatic strategies enabling the selective labeling of the protein N-terminal alpha-amine group are described. |
format | Online Article Text |
id | pubmed-8228110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82281102021-06-26 Exploiting Protein N-Terminus for Site-Specific Bioconjugation De Rosa, Lucia Di Stasi, Rossella Romanelli, Alessandra D’Andrea, Luca Domenico Molecules Review Although a plethora of chemistries have been developed to selectively decorate protein molecules, novel strategies continue to be reported with the final aim of improving selectivity and mildness of the reaction conditions, preserve protein integrity, and fulfill all the increasing requirements of the modern applications of protein conjugates. The targeting of the protein N-terminal alpha-amine group appears a convenient solution to the issue, emerging as a useful and unique reactive site universally present in each protein molecule. Herein, we provide an updated overview of the methodologies developed until today to afford the selective modification of proteins through the targeting of the N-terminal alpha-amine. Chemical and enzymatic strategies enabling the selective labeling of the protein N-terminal alpha-amine group are described. MDPI 2021-06-09 /pmc/articles/PMC8228110/ /pubmed/34207845 http://dx.doi.org/10.3390/molecules26123521 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review De Rosa, Lucia Di Stasi, Rossella Romanelli, Alessandra D’Andrea, Luca Domenico Exploiting Protein N-Terminus for Site-Specific Bioconjugation |
title | Exploiting Protein N-Terminus for Site-Specific Bioconjugation |
title_full | Exploiting Protein N-Terminus for Site-Specific Bioconjugation |
title_fullStr | Exploiting Protein N-Terminus for Site-Specific Bioconjugation |
title_full_unstemmed | Exploiting Protein N-Terminus for Site-Specific Bioconjugation |
title_short | Exploiting Protein N-Terminus for Site-Specific Bioconjugation |
title_sort | exploiting protein n-terminus for site-specific bioconjugation |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8228110/ https://www.ncbi.nlm.nih.gov/pubmed/34207845 http://dx.doi.org/10.3390/molecules26123521 |
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