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基孔肯雅病毒非结构蛋白功能域之间的网络映射

Network mapping among the functional domains of Chikungunya virus nonstructural proteins.

作者信息

Rana Jyoti, Rajasekharan Sreejith, Gulati Sahil, Dudha Namrata, Gupta Amita, Chaudhary Vijay Kumar, Gupta Sanjay

机构信息

Center for Emerging Diseases, Department of Biotechnology, Jaypee Institute of Information Technology, A-10, Noida, 201307, Uttar Pradesh, India.

出版信息

Proteins. 2014 Oct;82(10):2403-11. doi: 10.1002/prot.24602. Epub 2014 May 30.

Abstract

Formation of virus specific replicase complex is among the most important steps that determines the fate of viral transcription and replication during Chikungunya virus (CHIKV) infection. In the present study, the authors have computationally generated a 3D structure of CHIKV late replicase complex on the basis of the interactions identified among the domains of CHIKV nonstructural proteins (nsPs) which make up the late replicase complex. The interactions among the domains of CHIKV nsPs were identified using systems such as pull down, protein interaction ELISA, and yeast two-hybrid. The structures of nsPs were generated using I-TASSER and the biological assembly of the replicase complex was determined using ZRANK and RDOCK. A total of 36 interactions among the domains and full length proteins were tested and 12 novel interactions have been identified. These interactions included the homodimerization of nsP1 and nsP4 through their respective C-ter domains; the associations of nsP2 helicase domain and C-ter domain of nsP4 with methyltransferase and membrane binding domains of nsP1; the interaction of nsP2 protease domain with C-ter domain of nsP4; and the interaction of nsP3 macro and alphavirus unique domains with the C-ter domain of nsP1. The novel interactions identified in the current study form a network of organized associations that suggest the spatial arrangement of nsPs in the late replicase complex of CHIKV.

摘要

病毒特异性复制酶复合体的形成是决定基孔肯雅病毒(CHIKV)感染期间病毒转录和复制命运的最重要步骤之一。在本研究中,作者基于构成晚期复制酶复合体的CHIKV非结构蛋白(nsPs)结构域之间确定的相互作用,通过计算机模拟生成了CHIKV晚期复制酶复合体的三维结构。使用下拉法、蛋白质相互作用ELISA和酵母双杂交等系统确定了CHIKV nsPs结构域之间的相互作用。使用I-TASSER生成nsPs的结构,并使用ZRANK和RDOCK确定复制酶复合体的生物学组装。总共测试了结构域和全长蛋白之间的36种相互作用,确定了12种新的相互作用。这些相互作用包括nsP1和nsP4通过各自的C端结构域进行同源二聚化;nsP2解旋酶结构域和nsP4的C端结构域与nsP1的甲基转移酶和膜结合结构域的关联;nsP2蛋白酶结构域与nsP4的C端结构域的相互作用;以及nsP3的大结构域和甲病毒独特结构域与nsP1的C端结构域的相互作用。本研究中确定的新相互作用形成了一个有组织的关联网络,提示了CHIKV晚期复制酶复合体中nsPs的空间排列。

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