Mutation in the cytoplasmic retrieval signal of porcine epidemic diarrhea virus spike (S) protein is responsible for enhanced fusion activity

[1]  F. Taguchi,et al.  Role of Proteases in the Release of Porcine Epidemic Diarrhea Virus from Infected Cells , 2011, Journal of Virology.

[2]  T. Nunoya,et al.  Enhanced cell fusion activity in porcine epidemic diarrhea virus adapted to suckling mice , 2010, Archives of Virology.

[3]  F. Taguchi,et al.  Two-Step Conformational Changes in a Coronavirus Envelope Glycoprotein Mediated by Receptor Binding and Proteolysis , 2009, Journal of Virology.

[4]  S. Fukushi,et al.  Entry from the Cell Surface of Severe Acute Respiratory Syndrome Coronavirus with Cleaved S Protein as Revealed by Pseudotype Virus Bearing Cleaved S Protein , 2008, Journal of Virology.

[5]  M. Takeda,et al.  Efficient Multiplication of Human Metapneumovirus in Vero Cells Expressing the Transmembrane Serine Protease TMPRSS2 , 2008, Journal of Virology.

[6]  Larissa B. Thackray,et al.  Aromatic Amino Acids in the Juxtamembrane Domain of Severe Acute Respiratory Syndrome Coronavirus Spike Glycoprotein Are Important for Receptor-Dependent Virus Entry and Cell-Cell Fusion , 2008, Journal of Virology.

[7]  J. Li,et al.  The Cytoplasmic Tail of the Severe Acute Respiratory Syndrome Coronavirus Spike Protein Contains a Novel Endoplasmic Reticulum Retrieval Signal That Binds COPI and Promotes Interaction with Membrane Protein , 2006, Journal of Virology.

[8]  Wenhui Li,et al.  Conformational States of the Severe Acute Respiratory Syndrome Coronavirus Spike Protein Ectodomain , 2006, Journal of Virology.

[9]  F. Cosset,et al.  Important Role for the Transmembrane Domain of Severe Acute Respiratory Syndrome Coronavirus Spike Protein during Entry , 2006, Journal of Virology.

[10]  J. M. Melancon,et al.  Genetic analysis of the SARS-coronavirus spike glycoprotein functional domains involved in cell-surface expression and cell-to-cell fusion , 2005, Virology.

[11]  T. Mizutani,et al.  Vesicular stomatitis virus pseudotyped with severe acute respiratory syndrome coronavirus spike protein. , 2005, The Journal of general virology.

[12]  R. Sarisky,et al.  Use of a novel cell-based fusion reporter assay to explore the host range of human respiratory syncytial virus F protein , 2005, Virology Journal.

[13]  W. Wimley,et al.  The aromatic domain of the coronavirus class I viral fusion protein induces membrane permeabilization: putative role during viral entry. , 2005, Biochemistry.

[14]  M. Pensaert,et al.  A new coronavirus-like particle associated with diarrhea in swine , 2005, Archives of Virology.

[15]  L. Enjuanes,et al.  A Novel Sorting Signal for Intracellular Localization Is Present in the S Protein of a Porcine Coronavirus but Absent from Severe Acute Respiratory Syndrome-associated Coronavirus , 2004, Journal of Biological Chemistry.

[16]  C. Machamer,et al.  Intracellular Targeting Signals Contribute to Localization of Coronavirus Spike Proteins near the Virus Assembly Site , 2004, Journal of Virology.

[17]  R. Hodges,et al.  Structural Characterization of the SARS-Coronavirus Spike S Fusion Protein Core , 2004, Journal of Biological Chemistry.

[18]  M. Whitt,et al.  The Membrane-Proximal Region of Vesicular Stomatitis Virus Glycoprotein G Ectodomain Is Critical for Fusion and Virus Infectivity , 2003, Journal of Virology.

[19]  B. Bosch,et al.  The Coronavirus Spike Protein Is a Class I Virus Fusion Protein: Structural and Functional Characterization of the Fusion Core Complex , 2003, Journal of Virology.

[20]  F. Taguchi,et al.  Communication between S1N330 and a Region in S2 of Murine Coronavirus Spike Protein Is Important for Virus Entry into Cells Expressing CEACAM1b Receptor , 2002, Virology.

[21]  F. Taguchi,et al.  Functional analysis of an epitope in the S2 subunit of the murine coronavirus spike protein: involvement in fusion activity. , 2000, The Journal of general virology.

[22]  C. Machamer,et al.  Infectious Bronchitis Virus E Protein Is Targeted to the Golgi Complex and Directs Release of Virus-Like Particles , 2000, Journal of Virology.

[23]  Kevin W. Chang,et al.  Coronavirus-Induced Membrane Fusion Requires the Cysteine-Rich Domain in the Spike Protein , 2000, Virology.

[24]  O. Weisz,et al.  Oligomerization of a membrane protein correlates with its retention in the Golgi complex , 1993, The Journal of cell biology.

[25]  B. Hogue,et al.  The amino-terminal signal peptide on the porcine transmissible gastroenteritis coronavirus matrix protein is not an absolute requirement for membrane translocation and glycosylation , 1988, Virology.