Literature DB >> 11799197

Processing of nonstructural protein 1a of human astrovirus.

Ute Geigenmüller1, Teri Chew, Nancy Ginzton, Suzanne M Matsui.   

Abstract

Astrovirus contains three open reading frames (ORF) on its genomic RNA, ORF1a, ORF1b, and ORF2. ORF1a encodes a 920-amino-acid (aa) nonstructural protein, nsP1a, which displays a 3C-like serine protease motif. Little is known about the processing of nsP1a or whether the protease it contains is active and involved in autocatalytic processing. Here we address both of these matters. Intact and N-terminally deleted forms of ORF1a from human astrovirus serotype 1 were expressed in BHK cells, and nsP1a-derived processing products were immunoprecipitated with an nsP1a-specific antibody or an antibody specific for an N-terminally linked epitope tag. The mapping of the main processing products, p20 and p27, suggests cleavage sites near aa 170, 410, and 655 of nsP1a. Cleavages at around aa 410 and 655, but not aa 170, were abolished when a 9-aa substitution was introduced into the protease motif in nsP1a. The p27 processing product was also found in Caco-2 cells that had been infected with human astrovirus serotype 1, confirming the presence of the cleavage sites at approximately aa 410 and 655.

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Year:  2002        PMID: 11799197      PMCID: PMC135888          DOI: 10.1128/jvi.76.4.2003-2008.2002

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  19 in total

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Authors:  U K Laemmli
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  17 in total

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10.  Initiation of human astrovirus type 1 infection was blocked by inhibitors of phosphoinositide 3-kinase.

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