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Journal of General Virology (2002), 83, 1691-1695.
© 2002 Society for General Microbiology


Animal: RNA Viruses

Studies on intracellular processing of the capsid protein of human astrovirus serotype 1 in infected cells

Ute Geigenmüller1,2, Nancy H. Ginzton1,2 and Suzanne M. Matsui1,2

Department of Medicine, Gastroenterology Section (111-GI), VA Palo Alto Health Care System, 3801 Miranda Avenue, Palo Alto, CA 94304, USA1
Division of Gastroenterology and Hepatology, Stanford University School of Medicine, Stanford, CA, USA2

Author for correspondence: Suzanne Matsui (at VA Palo Alto Health Care System). Fax +1 650 852 3259. e-mail sumatsui{at}Stanford.edu

Astroviruses are non-enveloped, positive-strand RNA viruses. Their structural (capsid) protein is processed extracellularly into several smaller fragments which are found on the mature viral particle. In addition, intracellular cleavage of the capsid protein has been proposed. However, analysis of capsid protein processing has been hampered by the lack of antibodies to regions near the N and C termini of the protein. Here we describe the construction of two infectious mutants of human astrovirus serotype 1 (HAstV-1), in which amino acids (aa) 11–30 or aa 783–787, respectively, of the 787 aa capsid protein were replaced by tag sequences. Processing of the tagged capsid proteins in infected Caco-2 cells was analysed by immunoprecipitation with specific reagents directed against the tags or against native internal regions of the capsid protein. No intracellular processing of the capsid protein in infected cells could be detected, while assembled viral particles were readily observed within cells.




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