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首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Homotrpic interaction and multimerization of nucleocapsid protein of tomato spotted wilt tospovirus: Identification and characterization of two interacting domains
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Homotrpic interaction and multimerization of nucleocapsid protein of tomato spotted wilt tospovirus: Identification and characterization of two interacting domains

机译:番茄斑萎病毒的同质相互作用和核衣壳蛋白的多聚化:两个相互作用域的鉴定和表征

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摘要

The nucleocapsid protein (N) of tomato spot- ted wilt tospovirus (TSWV) plays a central role in the viral life cycle. With the aid of the yeast two-hybrid system and surface plasmon resonance analysis, homotypic interaction and mul- timerization of the N protein was detected. Analysis of deletion mutants identified two binding regions in the protein, located at the N terminus (amino acids 1-39) and the C terminus (amino acids 233-248) , respectively, implying a "head-to-tail" interaction of the N terminus with the C terminus to form a multimeric chain. Further characterization of the binding domains was performed by site-directed mutagenesis. Two phenylalanines (F242 and F246) highly conserved in the N proteins within the Tospovirus genus were shown to play a crucial role in the interaction.
机译:番茄斑点枯萎病毒(TSWV)的核衣壳蛋白(N)在病毒生命周期中起着核心作用。借助酵母双杂交系统和表面等离振子共振分析,检测了同型相互作用和N蛋白的多态性。缺失突变体的分析确定了蛋白质中的两个结合区,分别位于N末端(氨基酸1-39)和C末端(氨基酸233-248),这暗示了蛋白质的“头对尾”相互作用。 N末端与C末端形成多聚体链。结合结构域的进一步表征是通过定点诱变进行的。已显示在Tospovirus属的N蛋白中高度保守的两个苯丙氨酸(F242和F246)在相互作用中起关键作用。

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