Homotypic interaction and multimerization of nucleocapsid protein of tomato spotted wilt tospovirus: Identification and characterization of two interacting domains

被引:65
作者
Uhrig, JF
Soellick, TR
Minke, CJ
Philipp, C
Kellmann, JW
Schreier, PH
机构
[1] Max Planck Inst Zuchtungsforsch, Abt Genet Grundlagen Pflanzenzuchtung, D-50829 Cologne, Germany
[2] Bayer AG, PF F MWF BT, D-51368 Leverkusen, Germany
关键词
D O I
10.1073/pnas.96.1.55
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The nucleocapsid protein (N) of tomato spotted 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 multimerization 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.
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页码:55 / 60
页数:6
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