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肌动蛋白与登革病毒2型和4型包膜蛋白相互作用。

Actin Interacts with Dengue Virus 2 and 4 Envelope Proteins.

作者信息

Jitoboam Kunlakanya, Phaonakrop Narumon, Libsittikul Sirikwan, Thepparit Chutima, Roytrakul Sittiruk, Smith Duncan R

机构信息

Institute of Molecular Biosciences, Mahidol University, Salaya campus, 25/25 Phuttamonton Sai 4, Salaya, Nakorn Pathom, Thailand.

National Center for Genetic Engineering and Biotechnology (BIOTEC), National Science and Technology Development Agency, 113 Thailand Science Park, Phahonyothin Road, Khlong Nueng, Khlong Luang, Pathum Thani, Thailand.

出版信息

PLoS One. 2016 Mar 24;11(3):e0151951. doi: 10.1371/journal.pone.0151951. eCollection 2016.

Abstract

Dengue virus (DENV) remains a significant public health problem in many tropical and sub-tropical countries worldwide. The DENV envelope (E) protein is the major antigenic determinant and the protein that mediates receptor binding and endosomal fusion. In contrast to some other DENV proteins, relatively few cellular interacting proteins have been identified. To address this issue a co-immuoprecipitation strategy was employed. The predominant co-immunoprecipitating proteins identified were actin and actin related proteins, however the results suggested that actin was the only bona fide interacting partner. Actin was shown to interact with the E protein of DENV 2 and 4, and the interaction between actin and DENV E protein was shown to occur in a truncated DENV consisting of only domains I and II. Actin was shown to decrease during infection, but this was not associated with a decrease in gene transcription. Actin-related proteins also showed a decrease in expression during infection that was not transcriptionally regulated. Cytoskeletal reorganization was not observed during infection, suggesting that the interaction between actin and E protein has a cell type specific component.

摘要

登革病毒(DENV)在全球许多热带和亚热带国家仍然是一个重大的公共卫生问题。登革病毒包膜(E)蛋白是主要的抗原决定簇,也是介导受体结合和内体融合的蛋白。与其他一些登革病毒蛋白相比,已鉴定出的细胞相互作用蛋白相对较少。为了解决这个问题,采用了共免疫沉淀策略。鉴定出的主要共免疫沉淀蛋白是肌动蛋白和肌动蛋白相关蛋白,然而结果表明肌动蛋白是唯一真正的相互作用伙伴。已证明肌动蛋白与登革病毒2型和4型的E蛋白相互作用,并且肌动蛋白与登革病毒E蛋白之间的相互作用发生在仅由结构域I和II组成的截短登革病毒中。已证明肌动蛋白在感染期间减少,但这与基因转录的减少无关。肌动蛋白相关蛋白在感染期间也表现出表达减少,且不受转录调控。感染期间未观察到细胞骨架重组,这表明肌动蛋白与E蛋白之间的相互作用具有细胞类型特异性成分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/837f/4806980/041d7859f122/pone.0151951.g001.jpg

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