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Structures and Dynamics of Dengue Virus Nonstructural Membrane Proteins
Dengue virus is an important human pathogen threating people, especially in tropical and sub-tropical regions. The viral genome has one open reading frame and encodes one polyprotein which can be processed into structural and nonstructural (NS) proteins. Four of the seven nonstructural proteins, NS2...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8880049/ https://www.ncbi.nlm.nih.gov/pubmed/35207152 http://dx.doi.org/10.3390/membranes12020231 |
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author | Li, Qingxin Kang, Congbao |
author_facet | Li, Qingxin Kang, Congbao |
author_sort | Li, Qingxin |
collection | PubMed |
description | Dengue virus is an important human pathogen threating people, especially in tropical and sub-tropical regions. The viral genome has one open reading frame and encodes one polyprotein which can be processed into structural and nonstructural (NS) proteins. Four of the seven nonstructural proteins, NS2A, NS2B, NS4A and NS4B, are membrane proteins. Unlike NS3 or NS5, these proteins do not harbor any enzymatic activities, but they play important roles in viral replication through interactions with viral or host proteins to regulate important pathways and enzymatic activities. The location of these proteins on the cell membrane and the functional roles in viral replication make them important targets for antiviral development. Indeed, NS4B inhibitors exhibit antiviral activities in different assays. Structural studies of these proteins are hindered due to challenges in crystallization and the dynamic nature of these proteins. In this review, the function and membrane topologies of dengue nonstructural membrane proteins are presented. The roles of solution NMR spectroscopy in elucidating the structure and dynamics of these proteins are introduced. The success in the development of NS4B inhibitors proves that this class of proteins is an attractive target for antiviral development. |
format | Online Article Text |
id | pubmed-8880049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88800492022-02-26 Structures and Dynamics of Dengue Virus Nonstructural Membrane Proteins Li, Qingxin Kang, Congbao Membranes (Basel) Review Dengue virus is an important human pathogen threating people, especially in tropical and sub-tropical regions. The viral genome has one open reading frame and encodes one polyprotein which can be processed into structural and nonstructural (NS) proteins. Four of the seven nonstructural proteins, NS2A, NS2B, NS4A and NS4B, are membrane proteins. Unlike NS3 or NS5, these proteins do not harbor any enzymatic activities, but they play important roles in viral replication through interactions with viral or host proteins to regulate important pathways and enzymatic activities. The location of these proteins on the cell membrane and the functional roles in viral replication make them important targets for antiviral development. Indeed, NS4B inhibitors exhibit antiviral activities in different assays. Structural studies of these proteins are hindered due to challenges in crystallization and the dynamic nature of these proteins. In this review, the function and membrane topologies of dengue nonstructural membrane proteins are presented. The roles of solution NMR spectroscopy in elucidating the structure and dynamics of these proteins are introduced. The success in the development of NS4B inhibitors proves that this class of proteins is an attractive target for antiviral development. MDPI 2022-02-17 /pmc/articles/PMC8880049/ /pubmed/35207152 http://dx.doi.org/10.3390/membranes12020231 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Li, Qingxin Kang, Congbao Structures and Dynamics of Dengue Virus Nonstructural Membrane Proteins |
title | Structures and Dynamics of Dengue Virus Nonstructural Membrane Proteins |
title_full | Structures and Dynamics of Dengue Virus Nonstructural Membrane Proteins |
title_fullStr | Structures and Dynamics of Dengue Virus Nonstructural Membrane Proteins |
title_full_unstemmed | Structures and Dynamics of Dengue Virus Nonstructural Membrane Proteins |
title_short | Structures and Dynamics of Dengue Virus Nonstructural Membrane Proteins |
title_sort | structures and dynamics of dengue virus nonstructural membrane proteins |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8880049/ https://www.ncbi.nlm.nih.gov/pubmed/35207152 http://dx.doi.org/10.3390/membranes12020231 |
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