Literature DB >> 11807229

Hepatitis A virus polyprotein processing by Escherichia coli proteases.

Rosa M Pintó1, Susana Guix1, Juan F González-Dankaart1, Santiago Caballero1, Gloria Sánchez1, Ke-Jian Guo1, Enric Ribes1, Albert Bosch1.   

Abstract

Hepatitis A virus (HAV) encodes a single polyprotein, which is post-translationally processed. This processing represents an essential step in capsid formation. The virus possesses only one protease, 3C, responsible for all cleavages, except for that at the VP1/2A junction region, which is processed by cellular proteases. In this study, data demonstrates that HAV polyprotein processing by Escherichia coli protease(s) leads to the formation of particulate structures. P3 polyprotein processing in E. coli is not dependent on an active 3C protease: the same processing pattern is observed with wild-type 3C or with several 3C mutants. However, this processing pattern is temperature-dependent, since it differs at 37 or 42 degrees C. The bacterial protease(s) cleave scissile bonds other than those of HAV; this contributes to the low efficiency of particle formation.

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Year:  2002        PMID: 11807229     DOI: 10.1099/0022-1317-83-2-359

Source DB:  PubMed          Journal:  J Gen Virol        ISSN: 0022-1317            Impact factor:   3.891


  7 in total

1.  Antigenic hepatitis A virus structures may be produced in Escherichia coli.

Authors:  Glòria Sánchez; Santiago Caballero; Susana Guix; Albert Bosch; Rosa M Pintó
Journal:  Appl Environ Microbiol       Date:  2003-03       Impact factor: 4.792

2.  A single mutation in the glycophorin A binding site of hepatitis A virus enhances virus clearance from the blood and results in a lower fitness variant.

Authors:  M Isabel Costafreda; Enric Ribes; Angels Franch; Albert Bosch; Rosa M Pintó
Journal:  J Virol       Date:  2012-05-16       Impact factor: 5.103

3.  Use of fluorescence resonance energy transfer for rapid detection of enteroviral infection in vivo.

Authors:  Yu-Chen Hwang; Wilfred Chen; Marylynn V Yates
Journal:  Appl Environ Microbiol       Date:  2006-05       Impact factor: 4.792

4.  Hepatitis A virus adaptation to cellular shutoff is driven by dynamic adjustments of codon usage and results in the selection of populations with altered capsids.

Authors:  M Isabel Costafreda; Francisco J Pérez-Rodriguez; Lucía D'Andrea; Susana Guix; Enric Ribes; Albert Bosch; Rosa M Pintó
Journal:  J Virol       Date:  2014-02-19       Impact factor: 5.103

5.  Capsid region involved in hepatitis A virus binding to glycophorin A of the erythrocyte membrane.

Authors:  Glòria Sánchez; Lluís Aragonès; M Isabel Costafreda; Enric Ribes; Albert Bosch; Rosa M Pintó
Journal:  J Virol       Date:  2004-09       Impact factor: 5.103

6.  Molecular basis of the behavior of hepatitis a virus exposed to high hydrostatic pressure.

Authors:  Lucía D'Andrea; Francisco J Pérez-Rodríguez; M Isabel Costafreda; Nerea Beguiristain; Cristina Fuentes; Teresa Aymerich; Susana Guix; Albert Bosch; Rosa M Pintó
Journal:  Appl Environ Microbiol       Date:  2014-08-08       Impact factor: 4.792

7.  Improving virus production through quasispecies genomic selection and molecular breeding.

Authors:  Francisco J Pérez-Rodríguez; Lucía D'Andrea; Montserrat de Castellarnau; Maria Isabel Costafreda; Susana Guix; Enric Ribes; Josep Quer; Josep Gregori; Albert Bosch; Rosa M Pintó
Journal:  Sci Rep       Date:  2016-11-03       Impact factor: 4.379

  7 in total

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