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登革热病毒介导的膜融合:第一步。

Membrane fusion by dengue virus: The first step.

机构信息

Institute of Research, Development, and Innovation in Healthcare Biotechnology (IDiBE), Universitas "Miguel Hernández", E-03202 Elche-Alicante, Spain.

出版信息

Biochim Biophys Acta Biomembr. 2025 Jan;1867(1):184400. doi: 10.1016/j.bbamem.2024.184400. Epub 2024 Nov 8.

Abstract

Flaviviruses include important human pathogens such as Dengue, Zika, West Nile, Yellow fever, Japanese encephalitis, and Tick-borne encephalitis viruses as well as some emerging viruses that affect millions of people worldwide. They fuse their membrane with the late endosomal one in a pH-dependent way and therefore the merging of the membranes is one of the main goals for obtaining new antivirals. The envelope E protein, a membrane fusion protein, is accountable for fusion and encompasses different domains involved in the fusion mechanism, including the fusion peptide segment. In this work we have used molecular dynamics to study the interaction of the distal end of domain II of the DENV envelope E protein with a membrane like the late endosomal membrane in order to observe the initiation of membrane fusion carried out by a number of trimers of the DENV envelope E protein interacting with a complex biomembrane and demonstrate its feasibility. Our results demonstrate the likelihood of membrane disorganization and pore formation by trimer complex organization, the amino acids responsible for such condition and the secondary structure arrangements needed for such fundamental process. At the same time, we define new targets of the envelope E protein sequence which could permit designing potent antiviral bioactive molecules.

摘要

黄病毒包括登革热、寨卡、西尼罗河、黄热病、日本脑炎和蜱传脑炎病毒等重要的人类病原体,以及一些影响全球数百万人的新兴病毒。它们以 pH 依赖的方式将其膜与晚期内体膜融合,因此膜的融合是获得新抗病毒药物的主要目标之一。包膜 E 蛋白是一种膜融合蛋白,负责融合,并包含参与融合机制的不同结构域,包括融合肽段。在这项工作中,我们使用分子动力学研究了 DENV 包膜 E 蛋白结构域 II 远端与类似晚期内体膜的膜的相互作用,以观察由与复杂生物膜相互作用的多个 DENV 包膜 E 蛋白三聚体进行的膜融合的起始,并证明其可行性。我们的结果表明,三聚体复合物的组织可能导致膜去组织和孔形成,负责这种情况的氨基酸以及这种基本过程所需的二级结构排列。同时,我们定义了包膜 E 蛋白序列的新靶标,这可能允许设计有效的抗病毒生物活性分子。

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