To study paramyxovirus-medialed cell fusion it would be advantageous t
o express in a cell a single protein that could cause regulated syncyt
ium formation at neutral pH following a specific activation signal. We
have constructed two SV5 fusion (F) protein mutants that contain thre
e arginine residues in the cleavage site and two separate glycine to a
lanine changes in the fusion peptide. The mutants were expressed in CV
-1 cells using an SV40 recombinant virus vector. The mutant F proteins
required addition of exogenous trypsin to cleave F-0 to F-1 and F-2.
Massive syncytium formation occurred within 2-4 hr following addition
of trypsin to the SV40 recombinant F virus-infected CV-1 cells. (C) 19
95 Academic Press, Inc.