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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Royal Society of Chemistry
2021
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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. |
format | Online Article Text |
id | pubmed-8209628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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