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首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Identification of cellular proteins interacting with equine infectious anemia virus S2 protein.
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Identification of cellular proteins interacting with equine infectious anemia virus S2 protein.

机译:鉴定与马传染性贫血病毒S2蛋白相互作用的细胞蛋白。

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摘要

The macrophage-tropic lentivirus, equine infectious anemia virus (EIAV), encodes the small auxiliary protein S2 from a short open reading frame that overlaps the amino terminus of env EIAV S2 is dispensable for virus replication in cultured cells but is required for disease production. S2 is approximately 7 kDa and has no overall amino acid sequence homology to other cellular or viral proteins. Therefore it is likely that S2 plays a role as an adaptor protein. To further investigate S2 function we performed a yeast-2-hybrid screen to identify cellular proteins that interact with EIAV S2. The screen identified two human cellular proteins, amplified in osteosarcoma (OS-9) and proteasome 26S ATPase subunit 3 (PSMC3) that interact with S2. The equine homologues of these proteins were cloned and their interactions with S2 confirmed using co-immunoprecipitation assays. We identified two OS-9 isoforms that interact with S2 and a third splice variant that does not, indicating a region of OS-9 apparently required for the S2 interaction. The roles of these cellular proteins during EIAV infection have not been determined.
机译:嗜巨噬细胞慢病毒,马传染性贫血病毒(EIAV),从短的开放阅读框编码小的辅助蛋白S2,该阅读框与env EIAV S2的氨基末端重叠,可用于培养细胞中的病毒复制,但对于疾病产生是必需的。 S2约为7 kDa,与其他细胞或病毒蛋白没有整体氨基酸序列同源性。因此,S2可能起衔接蛋白的作用。为了进一步研究S2功能,我们进行了酵母2杂交筛选,以鉴定与EIAV S2相互作用的细胞蛋白。该筛查确定了两种人类细胞蛋白,它们在骨肉瘤(OS-9)和蛋白酶体26S ATPase亚基3(PSMC3)中扩增,并与S2相互作用。克隆了这些蛋白质的马同系物,并使用共免疫沉淀测定法证实了它们与S2的相互作用。我们确定了两个与S2相互作用的OS-9同工型和一个不与S2相互作用的剪接变体,这表明S2相互作用显然需要OS-9区域。这些细胞蛋白在EIAV感染过程中的作用尚未确定。

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