Literature DB >> 12873773

Viral fusion proteins: multiple regions contribute to membrane fusion.

Sergio G Peisajovich1, Yechiel Shai.   

Abstract

In recent years, the simple picture of a viral fusion protein interacting with the cell and/or viral membranes by means of only two localized segments (i.e. the fusion peptide and the transmembrane domain) has given way to a more complex picture in which multiple regions from the viral proteins interact with membranes. Indeed, possible roles in membrane binding and/or destabilization have been postulated for the N-terminal heptad repeats, pre-transmembrane segments, and other internal regions of fusion proteins from distant viruses (such as orthomyxo-, retro-, paramyxo-, or flaviviruses). This review focuses on the experimental evidence and functional models postulated so far about the role of these regions in the process of virus-induced membrane fusion.

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Year:  2003        PMID: 12873773     DOI: 10.1016/s0005-2736(03)00170-6

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  32 in total

1.  A capsid protein of nonenveloped Bluetongue virus exhibits membrane fusion activity.

Authors:  Mario Forzan; Christoph Wirblich; Polly Roy
Journal:  Proc Natl Acad Sci U S A       Date:  2004-02-04       Impact factor: 11.205

2.  HIV-1 fusion peptide targets the TCR and inhibits antigen-specific T cell activation.

Authors:  Francisco J Quintana; Doron Gerber; Sally C Kent; Irun R Cohen; Yechiel Shai
Journal:  J Clin Invest       Date:  2005-07-07       Impact factor: 14.808

3.  A GxxxG-like motif within HIV-1 fusion peptide is critical to its immunosuppressant activity, structure, and interaction with the transmembrane domain of the T-cell receptor.

Authors:  Omri Faingold; Tomer Cohen; Yechiel Shai
Journal:  J Biol Chem       Date:  2012-08-07       Impact factor: 5.157

4.  Identification of the membrane-active regions of the severe acute respiratory syndrome coronavirus spike membrane glycoprotein using a 16/18-mer peptide scan: implications for the viral fusion mechanism.

Authors:  Jaime Guillén; Ana J Pérez-Berná; Miguel R Moreno; José Villalaín
Journal:  J Virol       Date:  2005-02       Impact factor: 5.103

5.  HIV-1 gp41 and TCRalpha trans-membrane domains share a motif exploited by the HIV virus to modulate T-cell proliferation.

Authors:  Tomer Cohen; Shmuel Jaffe Cohen; Niv Antonovsky; Irun R Cohen; Yechiel Shai
Journal:  PLoS Pathog       Date:  2010-09-02       Impact factor: 6.823

6.  Interaction of poly(L-lysine)-g-poly(ethylene glycol) with supported phospholipid bilayers.

Authors:  Fernanda F Rossetti; Ilya Reviakine; Gábor Csúcs; Fabiano Assi; János Vörös; Marcus Textor
Journal:  Biophys J       Date:  2004-09       Impact factor: 4.033

7.  Antibodies generated in cats by a lipopeptide reproducing the membrane-proximal external region of the feline immunodeficiency virus transmembrane enhance virus infectivity.

Authors:  Simone Giannecchini; Anna Maria D'Ursi; Cinzia Esposito; Mario Scrima; Elisa Zabogli; Giulia Freer; Paolo Rovero; Mauro Bendinelli
Journal:  Clin Vaccine Immunol       Date:  2007-06-27

8.  Interaction of the most membranotropic region of the HCV E2 envelope glycoprotein with membranes. Biophysical characterization.

Authors:  Ana J Pérez-Berná; Jaime Guillén; Miguel R Moreno; Ana I Gómez-Sánchez; George Pabst; Peter Laggner; José Villalaín
Journal:  Biophys J       Date:  2008-03-13       Impact factor: 4.033

9.  Mutagenesis of the fusion peptide-like domain of hepatitis C virus E1 glycoprotein: involvement in cell fusion and virus entry.

Authors:  Hsiao-Fen Li; Chia-Hsuan Huang; Li-Shuang Ai; Chin-Kai Chuang; Steve S L Chen
Journal:  J Biomed Sci       Date:  2009-09-24       Impact factor: 8.410

10.  Screening a peptide library by DSC and SAXD: comparison with the biological function of the parent proteins.

Authors:  Ana J Pérez-Berná; George Pabst; Peter Laggner; José Villalaín
Journal:  PLoS One       Date:  2009-02-05       Impact factor: 3.240

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