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생화학분자생물학회 (Korean Society for Biochemistry and Molecular Biology)
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Biochemical Characterization of Exoribonuclease Encoded by SARS Coronavirus

  • Chen, Ping (State Key Laboratory of Virology and The Modern Virology Research Centre, College of Life Sciences, Wuhan University) ;
  • Jiang, Miao (State Key Laboratory of Virology and The Modern Virology Research Centre, College of Life Sciences, Wuhan University) ;
  • Hu, Tao (State Key Laboratory of Virology and The Modern Virology Research Centre, College of Life Sciences, Wuhan University) ;
  • Liu, Qingzhen (State Key Laboratory of Virology and The Modern Virology Research Centre, College of Life Sciences, Wuhan University) ;
  • Chen, Xiaojiang S. (Department of Molecular and Computational Biology, University of Southern California) ;
  • Guo, Deyin (State Key Laboratory of Virology and The Modern Virology Research Centre, College of Life Sciences, Wuhan University)
  • 발행 : 2007.09.30
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초록

The nsp14 protein is an exoribonuclease that is encoded by severe acute respiratory syndrome coronavirus (SARS-CoV). We have cloned and expressed the nsp14 protein in Escherichia coli, and characterized the nature and the role(s) of the metal ions in the reaction chemistry. The purified recombinant nsp14 protein digested a 5'-labeled RNA molecule, but failed to digest the RNA substrate that is modified with fluorescein group at the 3'-hydroxyl group, suggesting a 3'-to-5' exoribonuclease activity. The exoribonuclease activity requires $Mg^{2+}$ as a cofactor. Isothermal titration calorimetry (ITC) analysis indicated a two-metal binding mode for divalent cations by nsp14. Endogenous tryptophan fluorescence and circular dichroism (CD) spectra measurements showed that there was a structural change of nsp14 when binding with metal ions. We propose that the conformational change induced by metal ions may be a prerequisite for catalytic activity by correctly positioning the side chains of the residues located in the active site of the enzyme.

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참고문헌

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