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Asparaginyl endopeptidases: enzymology, applications and limitations

Asparaginyl endopeptidases (AEP) are cysteine proteases found in mammalian and plant cells. Several AEP isoforms from plant species were found to exhibit transpeptidase activity which is integral for the key head-to-tail cyclisation reaction during the biosynthesis of cyclotides. Since many plant AE...

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Detalles Bibliográficos
Autores principales: Tang, T. M. Simon, Luk, Louis Y. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8209628/
https://www.ncbi.nlm.nih.gov/pubmed/34037066
http://dx.doi.org/10.1039/d1ob00608h
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author Tang, T. M. Simon
Luk, Louis Y. P.
author_facet Tang, T. M. Simon
Luk, Louis Y. P.
author_sort Tang, T. M. Simon
collection PubMed
description Asparaginyl endopeptidases (AEP) are cysteine proteases found in mammalian and plant cells. Several AEP isoforms from plant species were found to exhibit transpeptidase activity which is integral for the key head-to-tail cyclisation reaction during the biosynthesis of cyclotides. Since many plant AEPs exhibit excellent enzyme kinetics for peptide ligation via a relatively short substrate recognition sequence, they have become appealing tools for peptide and protein modification. In this review, research focused on the enzymology of AEPs and their applications in polypeptide cyclisation and labelling will be presented. Importantly, the limitations of using AEPs and opportunities for future research and innovation will also be discussed.
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spelling pubmed-82096282021-06-29 Asparaginyl endopeptidases: enzymology, applications and limitations Tang, T. M. Simon Luk, Louis Y. P. Org Biomol Chem Chemistry Asparaginyl endopeptidases (AEP) are cysteine proteases found in mammalian and plant cells. Several AEP isoforms from plant species were found to exhibit transpeptidase activity which is integral for the key head-to-tail cyclisation reaction during the biosynthesis of cyclotides. Since many plant AEPs exhibit excellent enzyme kinetics for peptide ligation via a relatively short substrate recognition sequence, they have become appealing tools for peptide and protein modification. In this review, research focused on the enzymology of AEPs and their applications in polypeptide cyclisation and labelling will be presented. Importantly, the limitations of using AEPs and opportunities for future research and innovation will also be discussed. The Royal Society of Chemistry 2021-05-12 /pmc/articles/PMC8209628/ /pubmed/34037066 http://dx.doi.org/10.1039/d1ob00608h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Tang, T. M. Simon
Luk, Louis Y. P.
Asparaginyl endopeptidases: enzymology, applications and limitations
title Asparaginyl endopeptidases: enzymology, applications and limitations
title_full Asparaginyl endopeptidases: enzymology, applications and limitations
title_fullStr Asparaginyl endopeptidases: enzymology, applications and limitations
title_full_unstemmed Asparaginyl endopeptidases: enzymology, applications and limitations
title_short Asparaginyl endopeptidases: enzymology, applications and limitations
title_sort asparaginyl endopeptidases: enzymology, applications and limitations
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8209628/
https://www.ncbi.nlm.nih.gov/pubmed/34037066
http://dx.doi.org/10.1039/d1ob00608h
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