TY - JOUR
T1 - Dissection and identification of regions required to form pseudoparticles by the interaction between the nucleocapsid (N) and membrane (M) proteins of SARS coronavirus
AU - Hatakeyama, Seisuke
AU - Matsuoka, Yusuke
AU - Ueshiba, Hidehiro
AU - Komatsu, Nobukazu
AU - Itoh, Kyogo
AU - Shichijo, Shigeki
AU - Kanai, Takao
AU - Fukushi, Masaya
AU - Ishida, Isao
AU - Kirikae, Teruo
AU - Sasazuki, Takehiko
AU - Miyoshi-Akiyama, Tohru
N1 - Funding Information:
T.M.A was supported by a grant from the National Project on Protein Structural and Functional Analyses from the Ministry of Education, Culture, Sports, Science, and Technology (MEXT) of Japan. T.S was supported by grants from the National Institute of Biomedical Innovation Grant 04-02, and the Japan Science and Technology Agency (JST). We thank Ms. Naoko Ohnishi of Tokyo Women's Medical University for help with transmission electron microscopic analysis.
PY - 2008/10/10
Y1 - 2008/10/10
N2 - When expressed in mammalian cells, the nucleocapsid (N) and membrane (M) proteins of the severe acute respiratory syndrome coronavirus (SARS-CoV) are sufficient to form pseudoparticles. To identify region(s) of the N molecule required for pseudoparticle formation, we performed biochemical analysis of the interaction of N mutants and M in HEK293 cells. Using a peptide library derived from N, we found that amino acids 101-115 constituted a novel binding site for M. We examined the ability of N mutants to interact with M and form pseudoparticles, and our observations indicated that M bound to NΔ(101-115), N1-150, N151-300, and N301-422, but not to N1-150Δ(101-115). However, pseudoparticles were formed when NΔ(101-115) or N301-422, but not N1-150 or N151-300, were expressed with M in HEK293 cells. These results indicated that the minimum portion of N required for the interaction with M and pseudoparticle formation consists of amino acids 301-422.
AB - When expressed in mammalian cells, the nucleocapsid (N) and membrane (M) proteins of the severe acute respiratory syndrome coronavirus (SARS-CoV) are sufficient to form pseudoparticles. To identify region(s) of the N molecule required for pseudoparticle formation, we performed biochemical analysis of the interaction of N mutants and M in HEK293 cells. Using a peptide library derived from N, we found that amino acids 101-115 constituted a novel binding site for M. We examined the ability of N mutants to interact with M and form pseudoparticles, and our observations indicated that M bound to NΔ(101-115), N1-150, N151-300, and N301-422, but not to N1-150Δ(101-115). However, pseudoparticles were formed when NΔ(101-115) or N301-422, but not N1-150 or N151-300, were expressed with M in HEK293 cells. These results indicated that the minimum portion of N required for the interaction with M and pseudoparticle formation consists of amino acids 301-422.
UR - https://www.scopus.com/pages/publications/52049125442
UR - https://www.scopus.com/pages/publications/52049125442#tab=citedBy
U2 - 10.1016/j.virol.2008.07.012
DO - 10.1016/j.virol.2008.07.012
M3 - Article
C2 - 18703211
AN - SCOPUS:52049125442
SN - 0042-6822
VL - 380
SP - 99
EP - 108
JO - Virology
JF - Virology
IS - 1
ER -