首页> 外文期刊>Journal of proteome research >Characterization of the Interactome of the Porcine Reproductive and Respiratory Syndrome Virus Nonstructural Protein 2 Reveals the Hyper Variable Region as a Binding Platform for Association with 14-3-3 Proteins
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Characterization of the Interactome of the Porcine Reproductive and Respiratory Syndrome Virus Nonstructural Protein 2 Reveals the Hyper Variable Region as a Binding Platform for Association with 14-3-3 Proteins

机译:猪生殖和呼吸综合征病毒非结构蛋白2的相互作用的表征揭示超可变区作为与14-3-3蛋白关联的结合平台。

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摘要

Porcine reproductive and respiratory syndrome virus (PRRSV) is a major threat to the swine industry worldwide and hence global food security, exacerbated by a newly emerged highly pathogenic (HP-PRRSV) strain from China. PRRSV nonstructural protein 2 (nsp2) is a multifunctional polypeptide with strain-dependent influences on pathogenicity. A number of discrete functional regions have been identified on the protein. Quantitative label free proteomics was used to identify cellular binding partners of nsp2 expressed by HP-PRRSV. This allowed the identification of potential cellular interacting partners and the discrimination of nonspecific interactions. The interactome data were further investigated and validated using biological replicates and also compared with nsp2 from a low pathogenic (LP) strain of PRRSV. Validation included both forward and reverse pulldowns and confocal microscopy. The data indicated that nsp2 interacted with a number of cellular proteins including 14-3-3, CD2AP, and other components of cellular aggresomes. The hyper-variable region of nsp2 protein was identified as a binding platform for association with 14-3-3 proteins.
机译:猪繁殖与呼吸综合症病毒(PRRSV)是对全球养猪业的主要威胁,因此也是全球粮食安全的主要威胁,而中国新出现的高致病性(HP-PRRSV)株使这一问题更加恶化。 PRRSV非结构蛋白2(nsp2)是一种多功能多肽,对致病性具有菌株依赖性影响。在蛋白质上已鉴定出许多离散的功能区。使用无标签定量蛋白质组学来鉴定HP-PRRSV表达的nsp2的细胞结合伴侣。这可以识别潜在的细胞相互作用伴侣,并可以区分非特异性相互作用。使用生物学复制品进一步研究和验证了相互作用组数据,并与来自PRRSV的低致病性(LP)菌株的nsp2进行了比较。验证包括正向和反向下拉和共聚焦显微镜。数据表明,nsp2与许多细胞蛋白相互作用,包括14-3-3,CD2AP和细胞聚集体的其他成分。 nsp2蛋白的高变区被确定为与14-3-3蛋白缔合的结合平台。

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