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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...

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Detalles Bibliográficos
Autores principales: De Rosa, Lucia, Di Stasi, Rossella, Romanelli, Alessandra, D’Andrea, Luca Domenico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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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