Homotypic interaction and multimerization of nucleocapsid protein of tomato spotted wilt tospovirus: Identification and characterization of two interacting domains
Jf. Uhrig et al., Homotypic interaction and multimerization of nucleocapsid protein of tomato spotted wilt tospovirus: Identification and characterization of two interacting domains, P NAS US, 96(1), 1999, pp. 55-60
Citations number
36
Categorie Soggetti
Multidisciplinary
Journal title
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
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-hybr
id system and surface plasmon resonance analysis, homotypic interaction and
multimerization of the N protein was detected. Analysis of deletion mutant
s 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 domain
s was performed by site-directed mutagenesis. Two phenylalanines (F242 and
F246) highly conserved in the N proteins within the Tospovirus genus were s
hown to play a crucial role in the interaction.