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Methyltransferase‐Directed Labeling of Biomolecules and its Applications
Methyltransferases (MTases) form a large family of enzymes that methylate a diverse set of targets, ranging from the three major biopolymers to small molecules. Most of these MTases use the cofactor S‐adenosyl‐l‐Methionine (AdoMet) as a methyl source. In recent years, there have been significant eff...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5502580/ https://www.ncbi.nlm.nih.gov/pubmed/27943567 http://dx.doi.org/10.1002/anie.201608625 |
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author | Deen, Jochem Vranken, Charlotte Leen, Volker Neely, Robert K. Janssen, Kris P. F. Hofkens, Johan |
author_facet | Deen, Jochem Vranken, Charlotte Leen, Volker Neely, Robert K. Janssen, Kris P. F. Hofkens, Johan |
author_sort | Deen, Jochem |
collection | PubMed |
description | Methyltransferases (MTases) form a large family of enzymes that methylate a diverse set of targets, ranging from the three major biopolymers to small molecules. Most of these MTases use the cofactor S‐adenosyl‐l‐Methionine (AdoMet) as a methyl source. In recent years, there have been significant efforts toward the development of AdoMet analogues with the aim of transferring moieties other than simple methyl groups. Two major classes of AdoMet analogues currently exist: doubly‐activated molecules and aziridine based molecules, each of which employs a different approach to achieve transalkylation rather than transmethylation. In this review, we discuss the various strategies for labelling and functionalizing biomolecules using AdoMet‐dependent MTases and AdoMet analogues. We cover the synthetic routes to AdoMet analogues, their stability in biological environments and their application in transalkylation reactions. Finally, some perspectives are presented for the potential use of AdoMet analogues in biology research, (epi)genetics and nanotechnology. |
format | Online Article Text |
id | pubmed-5502580 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55025802017-08-02 Methyltransferase‐Directed Labeling of Biomolecules and its Applications Deen, Jochem Vranken, Charlotte Leen, Volker Neely, Robert K. Janssen, Kris P. F. Hofkens, Johan Angew Chem Int Ed Engl Reviews Methyltransferases (MTases) form a large family of enzymes that methylate a diverse set of targets, ranging from the three major biopolymers to small molecules. Most of these MTases use the cofactor S‐adenosyl‐l‐Methionine (AdoMet) as a methyl source. In recent years, there have been significant efforts toward the development of AdoMet analogues with the aim of transferring moieties other than simple methyl groups. Two major classes of AdoMet analogues currently exist: doubly‐activated molecules and aziridine based molecules, each of which employs a different approach to achieve transalkylation rather than transmethylation. In this review, we discuss the various strategies for labelling and functionalizing biomolecules using AdoMet‐dependent MTases and AdoMet analogues. We cover the synthetic routes to AdoMet analogues, their stability in biological environments and their application in transalkylation reactions. Finally, some perspectives are presented for the potential use of AdoMet analogues in biology research, (epi)genetics and nanotechnology. John Wiley and Sons Inc. 2017-04-10 2017-05-02 /pmc/articles/PMC5502580/ /pubmed/27943567 http://dx.doi.org/10.1002/anie.201608625 Text en © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Reviews Deen, Jochem Vranken, Charlotte Leen, Volker Neely, Robert K. Janssen, Kris P. F. Hofkens, Johan Methyltransferase‐Directed Labeling of Biomolecules and its Applications |
title | Methyltransferase‐Directed Labeling of Biomolecules and its Applications |
title_full | Methyltransferase‐Directed Labeling of Biomolecules and its Applications |
title_fullStr | Methyltransferase‐Directed Labeling of Biomolecules and its Applications |
title_full_unstemmed | Methyltransferase‐Directed Labeling of Biomolecules and its Applications |
title_short | Methyltransferase‐Directed Labeling of Biomolecules and its Applications |
title_sort | methyltransferase‐directed labeling of biomolecules and its applications |
topic | Reviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5502580/ https://www.ncbi.nlm.nih.gov/pubmed/27943567 http://dx.doi.org/10.1002/anie.201608625 |
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