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

被引:56
作者
Melikyan, GB
Barnard, RJO
Markosyan, RM
Young, JAT
Cohen, FS
机构
[1] Rush Med Coll, Dept Mol Biophys & Physiol, Chicago, IL 60612 USA
[2] Univ Wisconsin, Dept Oncol, Madison, WI 53706 USA
关键词
D O I
10.1128/JVI.78.7.3753-3762.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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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页码:3753 / 3762
页数:10
相关论文
共 47 条
[1]   Identification of a cellular receptor for subgroup E avian leukosis virus [J].
Adkins, HB ;
Brojatsch, J ;
Naughton, J ;
Rolls, MM ;
Pesola, JM ;
Young, JAT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (21) :11617-11622
[2]   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 [J].
Adkins, HB ;
Brojatsch, J ;
Young, JAT .
JOURNAL OF VIROLOGY, 2000, 74 (08) :3572-3578
[3]   Two functionally distinct forms of a retroviral receptor explain the nonreciprocal receptor interference among subgroups B, D, and E avian leukosis viruses [J].
Adkins, HB ;
Blacklow, SC ;
Young, JAT .
JOURNAL OF VIROLOGY, 2001, 75 (08) :3520-3526
[4]   A RECEPTOR FOR SUBGROUP-A ROUS-SARCOMA VIRUS IS RELATED TO THE LOW-DENSITY-LIPOPROTEIN RECEPTOR [J].
BATES, P ;
YOUNG, JAT ;
VARMUS, HE .
CELL, 1993, 74 (06) :1043-1051
[5]  
BLUMENTHAL R, 1987, J BIOL CHEM, V262, P13614
[6]   Retroviral vectors preloaded with a viral receptor-ligand bridge protein are targeted to specific cell types [J].
Boerger, AL ;
Snitkovsky, S ;
Young, JAT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (17) :9867-9872
[7]   POSTTRANSLATIONAL OLIGOMERIZATION AND COOPERATIVE ACID ACTIVATION OF MIXED INFLUENZA HEMAGGLUTININ TRIMERS [J].
BOULAY, F ;
DOMS, RW ;
WEBSTER, RG ;
HELENIUS, A .
JOURNAL OF CELL BIOLOGY, 1988, 106 (03) :629-639
[8]   CAR1, a TNFR-related protein, is a cellular receptor for cytopathic avian leukosis sarcoma viruses and mediates apoptosis [J].
Brojatsch, J ;
Naughton, J ;
Rolls, MM ;
Zingler, K ;
Young, JAT .
CELL, 1996, 87 (05) :845-855
[9]   The pathway of membrane fusion catalyzed by influenza hemagglutinin: Restriction of lipids, hemifusion, and lipidic fusion pore formation [J].
Chernomordik, LV ;
Frolov, VA ;
Leikina, E ;
Bronk, P ;
Zimmerberg, J .
JOURNAL OF CELL BIOLOGY, 1998, 140 (06) :1369-1382
[10]  
Cohen FS, 2002, CURR TOP MEMBR, V52, P501