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Journal of Virology, January 1999, p. 177-185, Vol. 73, No. 1
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Processing of the Human Coronavirus 229E Replicase Polyproteins
by the Virus-Encoded 3C-Like Proteinase: Identification of Proteolytic
Products and Cleavage Sites Common to pp1a and pp1ab
John
Ziebuhr* and
Stuart G.
Siddell
Institute of Virology, University of
Würzburg, 97078 Würzburg, Germany
Received 19 June 1998/Accepted 18 September 1998
Replicase gene expression by the human coronavirus 229E involves
the synthesis of two large polyproteins, pp1a and pp1ab. Experimental
evidence suggests that these precursor molecules are subject to
extensive proteolytic processing. In this study, we show that a
chymotrypsin-like enzyme, the virus-encoded 3C-like proteinase
(3CLpro), cleaves within a common region of pp1a and pp1ab
(amino acids 3490 to 4068) at four sites. trans-cleavage
assays revealed that polypeptides of 5, 23, 12, and 16 kDa are
processed from pp1a/pp1ab by proteolysis of the peptide bonds
Q3546/S3547, Q3629/S3630, Q3824/N3825, and Q3933/A3934. Relative rate
constants for the 3CLpro-mediated cleavages Q2965/A2966,
Q3267/S3268, Q3824/N3825, and Q3933/A3934 were derived by competition
experiments using synthetic peptides and recombinant
3CLpro. The results indicate that coronavirus cleavage
sites differ significantly with regard to their susceptibilities to
proteolysis by 3CLpro. Finally, immunoprecipitation with
specific rabbit antisera was used to detect the pp1a/pp1ab processing
end products in virus-infected cells, and immunofluorescence data that
suggest an association of these polypeptides with intracellular
membranes were obtained.
*
Corresponding author. Mailing address: Institute of
Virology, University of Würzburg, Versbacher Str. 7, 97078 Würzburg, Germany. Phone: 49-931-2013966. Fax: 49-931-2013934. E-mail: ziebuhr{at}vim.uni-wuerzburg.de.
Journal of Virology, January 1999, p. 177-185, Vol. 73, No. 1
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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