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N-Myristoyltransferase Is a Cell Wall Target in Aspergillus fumigatus
[Image: see text] Treatment of filamentous fungal infections relies on a limited repertoire of antifungal agents. Compounds possessing novel modes of action are urgently required. N-myristoylation is a ubiquitous modification of eukaryotic proteins. The enzyme N-myristoyltransferase (NMT) has been c...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4477619/ https://www.ncbi.nlm.nih.gov/pubmed/25706802 http://dx.doi.org/10.1021/cb5008647 |
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author | Fang, Wenxia Robinson, David A. Raimi, Olawale G. Blair, David E. Harrison, Justin R. Lockhart, Deborah E. A. Torrie, Leah S. Ruda, Gian Filippo Wyatt, Paul G. Gilbert, Ian H. van Aalten, Daan M. F. |
author_facet | Fang, Wenxia Robinson, David A. Raimi, Olawale G. Blair, David E. Harrison, Justin R. Lockhart, Deborah E. A. Torrie, Leah S. Ruda, Gian Filippo Wyatt, Paul G. Gilbert, Ian H. van Aalten, Daan M. F. |
author_sort | Fang, Wenxia |
collection | PubMed |
description | [Image: see text] Treatment of filamentous fungal infections relies on a limited repertoire of antifungal agents. Compounds possessing novel modes of action are urgently required. N-myristoylation is a ubiquitous modification of eukaryotic proteins. The enzyme N-myristoyltransferase (NMT) has been considered a potential therapeutic target in protozoa and yeasts. Here, we show that the filamentous fungal pathogen Aspergillus fumigatus possesses an active NMT enzyme that is essential for survival. Surprisingly, partial repression of the gene revealed downstream effects of N-myristoylation on cell wall morphology. Screening a library of inhibitors led to the discovery of a pyrazole sulphonamide compound that inhibits the enzyme and is fungicidal under partially repressive nmt conditions. Together with a crystallographic complex showing the inhibitor binding in the peptide substrate pocket, we provide evidence of NMT being a potential drug target in A. fumigatus. |
format | Online Article Text |
id | pubmed-4477619 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-44776192015-06-24 N-Myristoyltransferase Is a Cell Wall Target in Aspergillus fumigatus Fang, Wenxia Robinson, David A. Raimi, Olawale G. Blair, David E. Harrison, Justin R. Lockhart, Deborah E. A. Torrie, Leah S. Ruda, Gian Filippo Wyatt, Paul G. Gilbert, Ian H. van Aalten, Daan M. F. ACS Chem Biol [Image: see text] Treatment of filamentous fungal infections relies on a limited repertoire of antifungal agents. Compounds possessing novel modes of action are urgently required. N-myristoylation is a ubiquitous modification of eukaryotic proteins. The enzyme N-myristoyltransferase (NMT) has been considered a potential therapeutic target in protozoa and yeasts. Here, we show that the filamentous fungal pathogen Aspergillus fumigatus possesses an active NMT enzyme that is essential for survival. Surprisingly, partial repression of the gene revealed downstream effects of N-myristoylation on cell wall morphology. Screening a library of inhibitors led to the discovery of a pyrazole sulphonamide compound that inhibits the enzyme and is fungicidal under partially repressive nmt conditions. Together with a crystallographic complex showing the inhibitor binding in the peptide substrate pocket, we provide evidence of NMT being a potential drug target in A. fumigatus. American Chemical Society 2015-02-23 2015-06-19 /pmc/articles/PMC4477619/ /pubmed/25706802 http://dx.doi.org/10.1021/cb5008647 Text en Copyright © 2015 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Fang, Wenxia Robinson, David A. Raimi, Olawale G. Blair, David E. Harrison, Justin R. Lockhart, Deborah E. A. Torrie, Leah S. Ruda, Gian Filippo Wyatt, Paul G. Gilbert, Ian H. van Aalten, Daan M. F. N-Myristoyltransferase Is a Cell Wall Target in Aspergillus fumigatus |
title | N-Myristoyltransferase Is a Cell Wall Target in Aspergillus fumigatus |
title_full | N-Myristoyltransferase Is a Cell Wall Target in Aspergillus fumigatus |
title_fullStr | N-Myristoyltransferase Is a Cell Wall Target in Aspergillus fumigatus |
title_full_unstemmed | N-Myristoyltransferase Is a Cell Wall Target in Aspergillus fumigatus |
title_short | N-Myristoyltransferase Is a Cell Wall Target in Aspergillus fumigatus |
title_sort | n-myristoyltransferase is a cell wall target in aspergillus fumigatus |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4477619/ https://www.ncbi.nlm.nih.gov/pubmed/25706802 http://dx.doi.org/10.1021/cb5008647 |
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