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Protein Macrocyclization for Tertiary Structure Stabilization
Proteins possess unique molecular recognition capabilities and enzymatic activities, features that are usually tied to a particular tertiary structure. To make use of proteins for biotechnological and biomedical purposes, it is often required to enforce their tertiary structure in order to ensure su...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8453710/ https://www.ncbi.nlm.nih.gov/pubmed/34060202 http://dx.doi.org/10.1002/cbic.202100111 |
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author | Haim, Anissa Neubacher, Saskia Grossmann, Tom N. |
author_facet | Haim, Anissa Neubacher, Saskia Grossmann, Tom N. |
author_sort | Haim, Anissa |
collection | PubMed |
description | Proteins possess unique molecular recognition capabilities and enzymatic activities, features that are usually tied to a particular tertiary structure. To make use of proteins for biotechnological and biomedical purposes, it is often required to enforce their tertiary structure in order to ensure sufficient stability under the conditions inherent to the application of interest. The introduction of intramolecular crosslinks has proven efficient in stabilizing native protein folds. Herein, we give an overview of methods that allow the macrocyclization of expressed proteins, discussing involved reaction mechanisms and structural implications. |
format | Online Article Text |
id | pubmed-8453710 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84537102021-09-27 Protein Macrocyclization for Tertiary Structure Stabilization Haim, Anissa Neubacher, Saskia Grossmann, Tom N. Chembiochem Minireviews Proteins possess unique molecular recognition capabilities and enzymatic activities, features that are usually tied to a particular tertiary structure. To make use of proteins for biotechnological and biomedical purposes, it is often required to enforce their tertiary structure in order to ensure sufficient stability under the conditions inherent to the application of interest. The introduction of intramolecular crosslinks has proven efficient in stabilizing native protein folds. Herein, we give an overview of methods that allow the macrocyclization of expressed proteins, discussing involved reaction mechanisms and structural implications. John Wiley and Sons Inc. 2021-06-21 2021-09-02 /pmc/articles/PMC8453710/ /pubmed/34060202 http://dx.doi.org/10.1002/cbic.202100111 Text en © 2021 The Authors. ChemBioChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Minireviews Haim, Anissa Neubacher, Saskia Grossmann, Tom N. Protein Macrocyclization for Tertiary Structure Stabilization |
title | Protein Macrocyclization for Tertiary Structure Stabilization |
title_full | Protein Macrocyclization for Tertiary Structure Stabilization |
title_fullStr | Protein Macrocyclization for Tertiary Structure Stabilization |
title_full_unstemmed | Protein Macrocyclization for Tertiary Structure Stabilization |
title_short | Protein Macrocyclization for Tertiary Structure Stabilization |
title_sort | protein macrocyclization for tertiary structure stabilization |
topic | Minireviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8453710/ https://www.ncbi.nlm.nih.gov/pubmed/34060202 http://dx.doi.org/10.1002/cbic.202100111 |
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