首页 | 本学科首页   官方微博 | 高级检索  
     

传染性法氏囊病病毒VP4酵母双杂交诱饵载体的构建及互作宿主细胞蛋白的筛选
引用本文:王念,陈玉明,张礼洲,高立,卢珍,高玉龙,王永强,高宏雷,刘长军,崔红玉,王笑梅,祁小乐. 传染性法氏囊病病毒VP4酵母双杂交诱饵载体的构建及互作宿主细胞蛋白的筛选[J]. 中国畜牧兽医, 2015, 42(2): 317-323. DOI: 10.16431/j.cnki.1671-7236.2015.02.012
作者姓名:王念  陈玉明  张礼洲  高立  卢珍  高玉龙  王永强  高宏雷  刘长军  崔红玉  王笑梅  祁小乐
作者单位:中国农业科学院哈尔滨兽医研究所, 兽医生物技术国家重点实验室, 禽传染病研究室, 哈尔滨 150001
基金项目:现代农业产业技术体系建设专项基金(nycytx-42-G3-01);国家重点实验室基本科研业务费(SKLVBP201303)
摘    要:VP4蛋白(viral protein 4)是传染性法氏囊病病毒(infectious bursal disease virus,IBDV)编码的一种重要非结构蛋白,具有蛋白水解酶活性,剪切多聚蛋白pVP2-VP4-VP3释放出pVP2、VP4、VP3,对病毒蛋白成熟具有重要的作用。为了研究VP4蛋白与宿主细胞的相互作用,本研究将IBDV VP4基因克隆入pGBKT7,构建诱饵载体pGBGtVP4,自激活试验证明其无自激活活性,对酵母细胞没有毒性。运用酵母双杂交技术,从鸡胚成纤维细胞(CEF)文库中筛选VP4的互作蛋白,经初筛、测序和回转验证,获得22个候选互作宿主细胞蛋白,为深入研究IBDV VP4与宿主互作的效应和机制奠定了基础。

关 键 词:传染性法氏囊病病毒  VP4  酵母双杂交  诱饵载体  互作蛋白  
收稿时间:2014-08-13

Construction of Bait Vector of Infectious Bursal Disease Virus VP4 and Screening of the Interacted Proteins of Host Cell Using Yeast Two-hybrid System
WANG Nian,CHEN Yu-ming,ZHANG Li-zhou,GAO Li,LU Zhen,GAO Yu-long,WANG Yong-qiang,GAO Hong-lei,LIU Chang-jun,CUI Hong-yu,WANG Xiao-mei,QI Xiao-le. Construction of Bait Vector of Infectious Bursal Disease Virus VP4 and Screening of the Interacted Proteins of Host Cell Using Yeast Two-hybrid System[J]. China Animal Husbandry & Veterinary Medicine, 2015, 42(2): 317-323. DOI: 10.16431/j.cnki.1671-7236.2015.02.012
Authors:WANG Nian  CHEN Yu-ming  ZHANG Li-zhou  GAO Li  LU Zhen  GAO Yu-long  WANG Yong-qiang  GAO Hong-lei  LIU Chang-jun  CUI Hong-yu  WANG Xiao-mei  QI Xiao-le
Affiliation:Division of Avian Infectious Diseases, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute, Chinese Academy of Agriculture Sciences, Harbin 150001, China
Abstract:Viral protein 4 (VP4) is an important non-structural protein with proteolytic enzyme activity encoded by infectious bursal disease virus (IBDV) genome that catalyzes the hydrolysis of polyprotein pVP2-VP4-VP3 to form viral proteins pVP2,VP4,VP3,which plays an important role in the process of viral proteins maturity.To study the interaction between VP4 and the host cell,VP4 full-length cDNA sequence was amplified and inserted into pGBKT7 vector to construct a bait vector (pGBGtVP4).The result of autoactivation assay showed that pGBGtVP4 vector had no autoactivation and virulence in Y2H gold yeast cell.After screening,sequencing and confirming interaction,22 kinds of potential interacted proteins were obtained from the expression library of chicken embryo fibroblasts (CEF) using the matchmaker gold yeast two-hybrid system.This study laid the foundation for further researches on the effect and mechanism of the interaction of IBDV VP4 and its host cell.
Keywords:infectious bursal disease virus (IBDV)  VP4  yeast two-hybrid  bait vector  interacted protein
本文献已被 CNKI 等数据库收录!
点击此处可从《中国畜牧兽医》浏览原始摘要信息
点击此处可从《中国畜牧兽医》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号