EXCEED THE SPACE PROVIDED. The paramyxovirus family contains both established major human pathogens, including measles virus and respiratory syncytial virus, and newly emerged human pathogens, the Hendra and Nipah viruses. The fusion (F) proteins from paramyxoviruses promote fusion of viral and cellular membranes, an event that is both an essential step mediating entry of enveloped viruses into the host cell and an excellent model system for investigating the basic molecular events in membrane fusion processes. The long-term objective of this proposed research is to understand the precise mechanism(s) of the paramyxovirus F proteins in promotion of membrane fusion. The central hypothesis of this research proposal is that regions of the paramxyovirus F proteins that are critical for promotion of membrane fusion will be conserved between disparate members of the family, and that analysis of these regions will aid in understandingthe precise mechanisms of the F proteins in promotion of membrane fusion. The experiments in Specific Aim 1 will utilize transient expression systems and site-directed mutagencsis to analyzethe synthesis and processing of the F protein from Hendra virus, a recently discovered human pathogen. The research proposed in Specific Aim 2 will characterize the membrane fusion event promoted by the Hendra virus F protein, using several different membrane fusion assays which allow for examination of various stages of the reaction. Finally, the experiments in Specific Aim 3 will examine the effect of mutations in the SV5 F and Hendra F proteins in regions that show amino acid conservation throughout the paramyxovirusfamily, to determine whether these changes effect folding, protein processing or promotion of membrane fusion. Accomplishing these goals will provide crucial information on the processing and fusion-promotion activity of a paramyxovirus F protein from a newly emerged virus. In addition conserved regions of the F proteins that are important in function will be identified. The results of all of these studies will provide significant new information relevant to understanding specific molecular events involved in membrane fusion processes. PERFORMANCE S1TE(S) (organization, city, state) University of Kentucky. Lexineton. KY KEY PERSONNEL ========================================Section End===========================================

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
5R01AI051517-04
Application #
6878067
Study Section
Experimental Virology Study Section (EVR)
Program Officer
Cassetti, Cristina
Project Start
2002-05-15
Project End
2007-04-30
Budget Start
2005-05-01
Budget End
2006-04-30
Support Year
4
Fiscal Year
2005
Total Cost
$253,400
Indirect Cost
Name
University of Kentucky
Department
Biochemistry
Type
Schools of Medicine
DUNS #
939017877
City
Lexington
State
KY
Country
United States
Zip Code
40506
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El Najjar, Farah; Schmitt, Anthony P; Dutch, Rebecca Ellis (2014) Paramyxovirus glycoprotein incorporation, assembly and budding: a three way dance for infectious particle production. Viruses 6:3019-54
Masante, Cyril; El Najjar, Farah; Chang, Andres et al. (2014) The human metapneumovirus small hydrophobic protein has properties consistent with those of a viroporin and can modulate viral fusogenic activity. J Virol 88:6423-33

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