๐ Molecular cloning, expression, purification, and mass spectrometric characterization of 3C-like protease of SARS coronavirus
Severe acute respiratory syndrome (SARS) is an acute respiratory illness, which has broken out in China. It has been known that SARS coronavirus (SARS_CoV) is a novel human coronavirus and is responsible for SARS infection. Belonging to one of the major proteins associated with SARS_CoV, SARS 3C-like protease (SARS_3CLpro) functions as a cysteine protease engaging in the proteolytic cleavage of the viral precursor polyprotein to a series of functional proteins required for coronavirus replication and is considered as an appealing target for designing anti-SARS agents. To facilitate the studies regarding the functions and structures of SARS_3CLpro, in this report the synthetic genes encoding 3CLpro of SARS_CoV were assembled, and the plasmid was constructed using pQE30 as vector and expressed in Escherichia coli M15 cells. The highly yielded (โผ15 mg/L) expressed protease was purified by use of NTA-Ni2+ affinity chromatography and FPLC system, and its sequence was determined by LC/MS with the residue coverage of 46.4%. ยฉ 2003 Elsevier Inc.
keywords
๐ human coronavirus (623)
๐ virus replication (219)
๐ respiratory syndrome (2004)
๐ acute respiratory (1734)
author
๐ค Sun, Haifang
๐ค Luo, Haibin
๐ค Yu, Changying
๐ค Sun, Tao
๐ค Chen, Jing
๐ค Peng, Shuying
๐ค Qin, Jun
๐ค Shen, Jianhua
๐ค Yang, Yiming
๐ค Xie, Youhua
๐ค Chen, Kaixian
๐ค Wang, Yuan
๐ค Shen, Xu
๐ค Jiang, Hualiang
year
โฐ 2003
issn
๐ 10465928
volume
32
number
2
page
302-308
citedbycount
27
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