TY - JOUR
T1 - Generation of henipavirus nucleocapsid proteins in yeast Saccharomyces cerevisiae
AU - Juozapaitis, Mindaugas
AU - Serva, Andrius
AU - Zvirbliene, Aurelija
AU - Slibinskas, Rimantas
AU - Staniulis, Juozas
AU - Sasnauskas, Kestutis
AU - Shiell, Brian J.
AU - Wang, Lin Fa
AU - Michalski, Wojtek P.
PY - 2007/3
Y1 - 2007/3
N2 - Hendra and Nipah viruses are newly emerged, zoonotic viruses and their genomes have nucleotide and predicted amino acid homologies placing them in the family Paramyxoviridae. Currently these viruses are classified in the new genus Henipavirus, within the subfamily Paramyxovirinae, family Paramyxoviridae. The genes encoding HeV and NiV nucleocapsid proteins were cloned into the yeast Saccharomyces cerevisiae expression vector pFGG3 under control of GAL7 promoter. A high level of expression of these proteins (18-20 mg l-1 of yeast culture) was obtained. Mass spectrometric analysis confirmed the primary structure of both proteins with 92% sequence coverage obtained using MS/MS analysis. Electron microscopy demonstrated the assembly of typical herring-bone structures of purified recombinant nucleocapsid proteins, characteristic for other paramyxoviruses. The nucleocapsid proteins revealed stability in yeast and can be easily purified by cesium chloride gradient ultracentrifugation. HeV nucleocapsid protein was detected by sera derived from fruit bats, humans, horses infected with HeV, and NiV nucleocapsid protein was immunodetected with sera from, fruit bats, humans and pigs. The development of an efficient and cost-effective system for generation of henipavirus nucleocapsid proteins might help to improve reagents for diagnosis of viruses.
AB - Hendra and Nipah viruses are newly emerged, zoonotic viruses and their genomes have nucleotide and predicted amino acid homologies placing them in the family Paramyxoviridae. Currently these viruses are classified in the new genus Henipavirus, within the subfamily Paramyxovirinae, family Paramyxoviridae. The genes encoding HeV and NiV nucleocapsid proteins were cloned into the yeast Saccharomyces cerevisiae expression vector pFGG3 under control of GAL7 promoter. A high level of expression of these proteins (18-20 mg l-1 of yeast culture) was obtained. Mass spectrometric analysis confirmed the primary structure of both proteins with 92% sequence coverage obtained using MS/MS analysis. Electron microscopy demonstrated the assembly of typical herring-bone structures of purified recombinant nucleocapsid proteins, characteristic for other paramyxoviruses. The nucleocapsid proteins revealed stability in yeast and can be easily purified by cesium chloride gradient ultracentrifugation. HeV nucleocapsid protein was detected by sera derived from fruit bats, humans, horses infected with HeV, and NiV nucleocapsid protein was immunodetected with sera from, fruit bats, humans and pigs. The development of an efficient and cost-effective system for generation of henipavirus nucleocapsid proteins might help to improve reagents for diagnosis of viruses.
KW - Expression
KW - Henipavirus
KW - Nucleocapsid
KW - Nucleocapsid-like particles
UR - https://www.scopus.com/pages/publications/33846807793
U2 - 10.1016/j.virusres.2006.10.008
DO - 10.1016/j.virusres.2006.10.008
M3 - Article
C2 - 17123657
AN - SCOPUS:33846807793
SN - 0168-1702
VL - 124
SP - 95
EP - 102
JO - Virus Research
JF - Virus Research
IS - 1-2
ER -