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Protein N-myristoylation: functions and mechanisms in control of innate immunity
Protein N-myristoylation is an important fatty acylation catalyzed by N-myristoyltransferases (NMTs), which are ubiquitous enzymes in eukaryotes. Specifically, attachment of a myristoyl group is vital for proteins participating in various biological functions, including signal transduction, cellular...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7966921/ https://www.ncbi.nlm.nih.gov/pubmed/33731917 http://dx.doi.org/10.1038/s41423-021-00663-2 |
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author | Wang, Bin Dai, Tong Sun, Wenhuan Wei, Yujun Ren, Jiang Zhang, Long Zhang, Mengdi Zhou, Fangfang |
author_facet | Wang, Bin Dai, Tong Sun, Wenhuan Wei, Yujun Ren, Jiang Zhang, Long Zhang, Mengdi Zhou, Fangfang |
author_sort | Wang, Bin |
collection | PubMed |
description | Protein N-myristoylation is an important fatty acylation catalyzed by N-myristoyltransferases (NMTs), which are ubiquitous enzymes in eukaryotes. Specifically, attachment of a myristoyl group is vital for proteins participating in various biological functions, including signal transduction, cellular localization, and oncogenesis. Recent studies have revealed unexpected mechanisms indicating that protein N-myristoylation is involved in host defense against microbial and viral infections. In this review, we describe the current understanding of protein N-myristoylation (mainly focusing on myristoyl switches) and summarize its crucial roles in regulating innate immune responses, including TLR4-dependent inflammatory responses and demyristoylation-induced innate immunosuppression during Shigella flexneri infection. Furthermore, we examine the role of myristoylation in viral assembly, intracellular host interactions, and viral spread during human immunodeficiency virus-1 (HIV-1) infection. Deeper insight into the relationship between protein N-myristoylation and innate immunity might enable us to clarify the pathogenesis of certain infectious diseases and better harness protein N-myristoylation for new therapeutics. |
format | Online Article Text |
id | pubmed-7966921 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79669212021-03-17 Protein N-myristoylation: functions and mechanisms in control of innate immunity Wang, Bin Dai, Tong Sun, Wenhuan Wei, Yujun Ren, Jiang Zhang, Long Zhang, Mengdi Zhou, Fangfang Cell Mol Immunol Review Article Protein N-myristoylation is an important fatty acylation catalyzed by N-myristoyltransferases (NMTs), which are ubiquitous enzymes in eukaryotes. Specifically, attachment of a myristoyl group is vital for proteins participating in various biological functions, including signal transduction, cellular localization, and oncogenesis. Recent studies have revealed unexpected mechanisms indicating that protein N-myristoylation is involved in host defense against microbial and viral infections. In this review, we describe the current understanding of protein N-myristoylation (mainly focusing on myristoyl switches) and summarize its crucial roles in regulating innate immune responses, including TLR4-dependent inflammatory responses and demyristoylation-induced innate immunosuppression during Shigella flexneri infection. Furthermore, we examine the role of myristoylation in viral assembly, intracellular host interactions, and viral spread during human immunodeficiency virus-1 (HIV-1) infection. Deeper insight into the relationship between protein N-myristoylation and innate immunity might enable us to clarify the pathogenesis of certain infectious diseases and better harness protein N-myristoylation for new therapeutics. Nature Publishing Group UK 2021-03-17 2021-04 /pmc/articles/PMC7966921/ /pubmed/33731917 http://dx.doi.org/10.1038/s41423-021-00663-2 Text en © The Author(s), under exclusive licence to CSI and USTC 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Review Article Wang, Bin Dai, Tong Sun, Wenhuan Wei, Yujun Ren, Jiang Zhang, Long Zhang, Mengdi Zhou, Fangfang Protein N-myristoylation: functions and mechanisms in control of innate immunity |
title | Protein N-myristoylation: functions and mechanisms in control of innate immunity |
title_full | Protein N-myristoylation: functions and mechanisms in control of innate immunity |
title_fullStr | Protein N-myristoylation: functions and mechanisms in control of innate immunity |
title_full_unstemmed | Protein N-myristoylation: functions and mechanisms in control of innate immunity |
title_short | Protein N-myristoylation: functions and mechanisms in control of innate immunity |
title_sort | protein n-myristoylation: functions and mechanisms in control of innate immunity |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7966921/ https://www.ncbi.nlm.nih.gov/pubmed/33731917 http://dx.doi.org/10.1038/s41423-021-00663-2 |
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