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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...

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Detalles Bibliográficos
Autores principales: Haim, Anissa, Neubacher, Saskia, Grossmann, Tom N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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.
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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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