Synthesis of recombinant human parainfluenza virus 1 and 3 nucleocapsid proteins in yeast Saccharomyces cerevisiae

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• 作者：Mindaugas Juozapaitis ; Aurelija Zvirbliene ; Indre Kucinskaite ; Indre Sezaite ; Rimantas Slibinskas ; Mayte Coiras ; Fern ; o de Ory Manchon ; Marí ; a Rosa Ló ; pez-Huertas ; Pilar Pé ; rez-Breñ ; a
• 关键词：Human parainfluenza viruses (HPIV1 ; HPIV3) ; Nucleocapsid ; Expression ; Yeast ; Nucleocapsid-like particles (NLPs) ; ELISA
• 刊名：Virus Research
• 出版年：2008
• 出版时间：May 2008
• 年：2008
• 卷：133
• 期：2
• 页码：178-186
• 全文大小：823 K

文摘

Human parainfluenza virus types 1 and 3 (HPIV1 and HPIV3, respectively), members of the virus family Paramyxoviridae, are common causes of lower respiratory tract infections in infants, young children, the immunocompromised, the chronically ill, and the elderly. In order to synthesize recombinant HPIV1 and HPIV3 nucleocapsid proteins, the coding sequences were cloned into the yeast Saccharomyces cerevisiae expression vector pFGG3 under control of GAL7 promoter. A high level of recombinant virus nucleocapsid proteins expression (20–24 mg l⁻¹ of yeast culture) was obtained. Electron microscopy demonstrated the assembly of typical herring-bone structures of purified recombinant nucleocapsid proteins, characteristic for other paramyxoviruses. These structures contained host RNA, which was resistant to RNase treatment. The nucleocapsid proteins were stable in yeast and were easily purified by caesium chloride gradient ultracentrifugation. Therefore, this system proved to be simple, efficient and cost-effective, suitable for high-level production of parainfluenza virus nucleocapsids as nucleocapsid-like particles. When used as coating antigens in an indirect ELISA, the recombinant N proteins reacted with sera of patients infected with HPIV1 or 3. Serological assays to detect HPIV-specific antibodies could be designed on this basis.