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. 2004 Nov;36(11):754–758. doi: 10.1093/abbs/36.11.754

Expression, Purification and Sublocalization of SARS-CoV Nucleocapsid Protein in Insect Cells

Ai-Xia Ren 1,2, You-Hua Xie 2, Yu-Ying Kong 2, Guan-Zhen Yang 2, Yao-Zhou Zhang 1,3,*, Yuan Wang 2,*, Xiang-Fu Wu 2,3,*
Editor: Zu-Xun Gong
PMCID: PMC7110235  PMID: 15514849

Abstract

The causative agent of severe acute respiratory syndrome (SARS) is a previously unidentified coronavirus, SARS-CoV. The nucleocapsid (N) protein of SARS-CoV is a major viral protein recognized by acute and early convalescent sera from SARS patients. To facilitate the studies on the function and structure of the N protein, this report describe the expression and purification of recombinant SARS-CoV N protein using the baculovirus expression system. Recombinant hexa-histidine-tagged N protein with a molecular mass of 47 kD was produced in insect cells. Recombinant N protein was purified to near homogeneity by Ni2+-NTA affinity chromatography. In addition, we examined the subcellular localization of the N protein by confocal microscopy in Trichoplusia ni BT1 Tn 5B1–4 cells infected with recombinant baculovirus. The N protein was found localized in the cytoplasm as well as in the nucleolus. The purified recombinant N protein can be used in further functional study of SARS-CoV.

Keywords: severe acute respiratory syndrome (SARS), SARS coronavirus, nucleocapsid protein, baculovirus, insect cells


Articles from Acta Biochimica et Biophysica Sinica are provided here courtesy of Oxford University Press

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