Literature DB >> 15016895

Low pH is required for avian sarcoma and leukosis virus Env-induced hemifusion and fusion pore formation but not for pore growth.

G B Melikyan1, R J O Barnard, R M Markosyan, J A T Young, F S Cohen.   

Abstract

Binding of avian sarcoma and leukosis virus (ASLV) to its cognate receptor on the cell surface causes conformational changes in its envelope protein (Env). It is currently debated whether low pH is required for ASLV infection. To elucidate the role of low pH, we studied the association between ASLV subgroup B (ASLV-B) and liposomes and fusion between effector cells expressing Env from ASLV-A and ASLV-B and target cells expressing cognate receptors. Neither EnvA nor EnvB promoted cell-cell fusion at neutral pH, but lowering the pH resulted in quick and extensive fusion. As expected for a low-pH-triggered reaction, fusion was a steep function of pH. Steps that required low pH were identified. Binding a soluble form of the receptor caused ASLV-B to hydrophobically associate with liposome membranes at neutral pH, indicating that low pH is not required for insertion of Env's fusion peptides into membranes. But both cell-cell hemifusion and fusion pore formation were pH dependent. It is proposed that fusion peptide insertion stabilizes the conformation of ASLV Env into a form that can be acted upon by low pH. At this point, but not before, low pH can induce fusion and is in fact required for fusion to occur. However, low pH is no longer necessary after formation of the initial fusion pore: pore enlargement does not require low pH.

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Year:  2004        PMID: 15016895      PMCID: PMC371058          DOI: 10.1128/jvi.78.7.3753-3762.2004

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


  45 in total

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2.  Soluble receptor-induced retroviral infection of receptor-deficient cells.

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3.  Targeting retroviral vector infection to cells that express heregulin receptors using a TVA-heregulin bridge protein.

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4.  A fifteen-amino-acid TVB peptide serves as a minimal soluble receptor for subgroup B avian leukosis and sarcoma viruses.

Authors:  Daniel J Knauss; John A T Young
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5.  A TVA-single-chain antibody fusion protein mediates specific targeting of a subgroup A avian leukosis virus vector to cells expressing a tumor-specific form of epidermal growth factor receptor.

Authors:  S Snitkovsky; T M Niederman; B S Carter; R C Mulligan; J A Young
Journal:  J Virol       Date:  2000-10       Impact factor: 5.103

6.  Targeting avian leukosis virus subgroup A vectors by using a TVA-VEGF bridge protein.

Authors:  S Snitkovsky; T M Niederman; R C Mulligan; J A Young
Journal:  J Virol       Date:  2001-02       Impact factor: 5.103

7.  Retroviral entry mediated by receptor priming and low pH triggering of an envelope glycoprotein.

Authors:  W Mothes; A L Boerger; S Narayan; J M Cunningham; J A Young
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8.  Two functionally distinct forms of a retroviral receptor explain the nonreciprocal receptor interference among subgroups B, D, and E avian leukosis viruses.

Authors:  H B Adkins; S C Blacklow; J A Young
Journal:  J Virol       Date:  2001-04       Impact factor: 5.103

9.  Identification and characterization of a shared TNFR-related receptor for subgroup B, D, and E avian leukosis viruses reveal cysteine residues required specifically for subgroup E viral entry.

Authors:  H B Adkins; J Brojatsch; J A Young
Journal:  J Virol       Date:  2000-04       Impact factor: 5.103

10.  Evidence that the transition of HIV-1 gp41 into a six-helix bundle, not the bundle configuration, induces membrane fusion.

Authors:  G B Melikyan; R M Markosyan; H Hemmati; M K Delmedico; D M Lambert; F S Cohen
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  41 in total

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2.  Stochastic entry of enveloped viruses: fusion versus endocytosis.

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Journal:  Biophys J       Date:  2007-05-18       Impact factor: 4.033

3.  Heptad repeat-derived peptides block protease-mediated direct entry from the cell surface of severe acute respiratory syndrome coronavirus but not entry via the endosomal pathway.

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4.  pH-dependence of intermediate steps of membrane fusion induced by the influenza fusion peptide.

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Journal:  Biochem J       Date:  2006-06-15       Impact factor: 3.857

Review 5.  Structures and mechanisms of viral membrane fusion proteins: multiple variations on a common theme.

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6.  pH regulation in early endosomes and interferon-inducible transmembrane proteins control avian retrovirus fusion.

Authors:  Tanay M Desai; Mariana Marin; Caleb Mason; Gregory B Melikyan
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7.  Hepatitis C virus is primed by CD81 protein for low pH-dependent fusion.

Authors:  Nishi R Sharma; Guaniri Mateu; Marlene Dreux; Arash Grakoui; François-Loïc Cosset; Gregory B Melikyan
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8.  A study of low pH-induced refolding of Env of avian sarcoma and leukosis virus into a six-helix bundle.

Authors:  R M Markosyan; P Bates; F S Cohen; G B Melikyan
Journal:  Biophys J       Date:  2004-08-31       Impact factor: 4.033

9.  Membrane-anchored inhibitory peptides capture human immunodeficiency virus type 1 gp41 conformations that engage the target membrane prior to fusion.

Authors:  Gregory B Melikyan; Marc Egelhofer; Dorothee von Laer
Journal:  J Virol       Date:  2006-04       Impact factor: 5.103

10.  Cell-specific targeting of lentiviral vectors mediated by fusion proteins derived from Sindbis virus, vesicular stomatitis virus, or avian sarcoma/leukosis virus.

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