Roles for the cytoplasmic tails of the fusion and hemagglutinin-neuraminidase proteins in budding of the paramyxovirus simian virus 5

Journal of Virology

Volumn 76, Issue 18, 2002, Pages 9284-9297

  Waning, David L ^a   Schmitt, Anthony P ^a   Leser, George P ^a   Lamb, Robert A ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HEMAGGLUTININ; HYBRID PROTEIN; SIALIDASE; VIRUS PROTEIN;

ANIMAL CELL; ARTICLE; CELL BUDDING; GENE DELETION; NONHUMAN; PARAMYXOVIRUS; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN PROTEIN INTERACTION; TISSUE CULTURE; VIRUS ASSEMBLY; VIRUS ENVELOPE; VIRUS INFECTION; VIRUS NUCLEOCAPSID; VIRUS PARTICLE;

AMINO ACID SEQUENCE; ANIMALS; CELL FUSION; CELL LINE; HN PROTEIN; MOLECULAR SEQUENCE DATA; MUTATION; RECOMBINATION, GENETIC; RUBULAVIRUS; SUBCELLULAR FRACTIONS; VIRAL FUSION PROTEINS; VIRUS ASSEMBLY; VIRUS REPLICATION;

EID: 0036720806     PISSN: 0022538X     EISSN: None     Source Type: Journal    
DOI: 10.1128/JVI.76.18.9284-9297.2002     Document Type: Article

References (64)

1. Assembly of Sendai virus: M protein interacts with F and HN proteins and with the cytoplasmic tail and transmembrane domain of F protein
2. Truncation of the COOH-terminal region of the paramyxovirus SV5 fusion protein leads to hemifusion but not complete fusion
3. Lipid raft microdomains: A gateway for compartmentalized trafficking of Ebola and Marburg viruses
4. Generation of bovine respiratory syncytial virus (BRSV) from cDNA: BRSV NS2 is not essential for virus replication in tissue culture, and the human RSV leader region acts as a functional BRSV genome promoter
5. The rule of six, a basic feature for efficient replication of Sendai virus defective interfering RNA
6. A matrix-less measles virus is infectious and elicits extensive cell fusion: Consequences for propagation in the brain
7. Measles viruses with altered envelope protein cytoplasmic tails gain cell fusion competence
8. Human parainfluenza virus type 1 matrix and nucleoprotein genes transiently expressed in mammalian cells induce the release of virus-like particles containing nucleocapsid-like structures
9. The GAG precursor of simian immunodeficiency virus assembles into virus-like particles
10. Overexpression of the N-terminal domain of TSG101 inhibits HIV-1 budding by blocking late domain function
11. Paramyxovirus fusion (F) protein: A conformational change on cleavage activation
12. Deletion of the cytoplasmic tail of the fusion protein of the paramyxovirus simian virus 5 affects fusion pore enlargement
13. Structure-function analysis of the Sendai virus F and HN cytoplasmic domain: Different role for the two proteins in the production of virus particle
14. 7 RNA polymerase
15. The cytoplasmic tail of the neuraminidase protein of influenza A virus does not play an important role in the packaging of this protein into viral envelopes
16. Tsg101 and the vacuolar protein sorting pathway are essential for HIV-1 budding
17. gag virus-like particles from recombinant baculovirus-infected cells
18. Retroviridae: The retroviruses and their replication
19. Influenza virus matrix protein is the major driving force in virus budding
20. Rhabdoviruses and the cellular ubiquitin-proteasome system: A budding interaction
21. A PPxY motif within the VP40 protein of Ebola virus interacts physically and functionally with a ubiquitin ligase: Implications for filovirus budding
22. A proline-rich motif within the matrix protein of vesicular stomatitis virus and rabies virus inter-acts with WW domains of cellular proteins: Implications for viral budding
23. The paramyxovirus SV5 small hydrophobic (SH) protein is not essential for virus growth in tissue culture cells
24. The SH integral membrane protein of the paramyxovirus simian virus 5 is required to block apoptosis in MDBK cells
25. Recovery of infectious SV5 from cloned DNA and expression of a foreign gene
26. Studies on the fusion peptide of a paramyxovirus fusion glycoprotein: Roles of conserved residues in cell fusion
27. Ebola virus VP40-induced particle formation and association with the lipid bilayer
28. The influenza virus hemagglutinin cytoplasmic tail is not essential for virus assembly or infectivity
29. Influenza virus hemagglutinin and neuraminidase cytoplasmic tails control particle shape
30. Membrane vesiculation function and exocytosis of wild-type and mutant matrix proteins of vesicular stomatitis virus
31. Paramyxoviridae: The viruses and their replication
32. Formation of wild-type and chimeric influenza virus-like particles following simultaneous expression of only four structural proteins
33. Viral liposomes released from insect cells infected with recombinant baculovirus expressing the matrix protein of vesicular stomatitis virus
34. The paramyxovirus simian virus 5 V protein slows progression of the cell cycle
35. HIV-1 and Ebola virus encode small peptide motifs that recruit Tsg101 to sites of particle assembly to facilitate egress
36. Budding of rabies virus particles in the absence of the spike glycoprotein
37. Matrix protein of rabies virus is responsible for the assembly and budding of bullet-shaped particles and interacts with the transmembrane spike glycoprotein G
38. The cytoplasmic tail of influenza A virus neuraminidase (NA) affects NA incorporation into virions, virion morphology, and virulence in mice but is not essential for virus replication
39. A comparison of the polypeptides of four measles virus strains
40. RNA replication for the paramyxovirus simian virus 5 requries an internal repeated (CGNNNN) sequence motif
41. Plasmid-driven formation of influenza virus-like particles
42. Efficient selection for high-expression transfectants with a novel eukaryotic vector
43. Fusion protein of the paramyxovirus simian virus 5: Nucleotide sequence of mRNA predicts a highly hydrophobic glycoprotein
44. The molecular biology of influenza viruses and paramyxoviruses
45. Comparison of the relative roles of the F and HN surface glycoproteins of the paramyxovirus simian virus 5 in inducing protective immunity
46. Isolation and characterization of monoclonal antibodies to simian virus 5 and their use in revealing antigenic differences between human, canine and simian isolates
47. A simple method of estimating fifty per cent endpoints
48. The membrane-proximal stem region of vesicular stomatitis virus G protein confers efficient virus assembly
49. A new cationic liposome reagent mediating nearly quantitative transfection of animal cells
50. Rhabdoviridae: The viruses and their replication
51. Sendai virus M protein binds independently to either the F or the HN glycoprotein in vivo
52. Involvement of the cytoplasmic domain of the hemagglutinin-neuraminidase protein in assembly of the paramyxovirus simian virus 5
53. Requirements for budding of paramyxovirus simian virus 5 virus-like particles
54. Requirement for a non-specific glycoprotein cytoplasmic domain sequence to drive efficient budding of vesicular stomatitis virus
55. Construction of a novel virus that targets HIV-1-infected cells and controls HIV-1 infection
56. Sequence characterization of the membrane protein gene of paramyxovirus simian virus 5
57. The major glycoprotein of Sendai virus is dispensable for efficient virus particle budding
58. Spike protein-nucleocapsid interactions drive the budding of alphaviruses
59. Cytoplasmic domain of Sendai virus HN protein contains a specific sequence required for its incorporation into virions
60. Role of matrix and fusion proteins in budding of Sendai virus
61. Vesicular release of Ebola virus matrix protein VP40
62. Gag
63. Glycoprotein cytoplasmic domain sequences required for rescue of a vesicular stomatitis virus glyco-protein mutant
64. A tyrosine-based motif in the cytoplasmic domain of the alphavirus envelope protein is essential for budding