Qz. Yao et Rw. Compans, PEPTIDES CORRESPONDING TO THE HEPTAD REPEAT SEQUENCE OF HUMAN PARAINFLUENZA VIRUS FUSION PROTEIN ARE POTENT INHIBITORS OF VIRUS-INFECTION, Virology, 223(1), 1996, pp. 103-112
It has been suggested that a conserved heptad repeat region in paramyx
ovirus fusion (F) proteins is essential for viral fusion activity (Buc
kland et al., 1992; Sergel et al., 1994; Reitter et al., 1995). We hav
e studied synthetic peptides containing the heptad repeat regions deri
ved from the F proteins of human parainfluenza virus type 2 (P12) and
type 3 (P13) for their function as potential inhibitors of virus-induc
ed cell fusion as well as their effects on spread of viral infection.
Two peptides containing sequences of heptad repeat B, adjacent to the
transmembrane domain of the F protein, were synthesized for both P12 a
nd P13 F proteins. We observed that the longer peptides [34 amino acid
s (a.a.) for P12F or 35 a.a. for P13F] which extend from heptad repeat
B to the transmembrane domain showed complete inhibition of cell fusi
on induced by the respective virus as well as by the vaccinia-expresse
d F and HN proteins. The 50% effective concentration to inhibit virus-
induced cell fusion was 2.1 mu M for P12 and 1.2 mu M for P13. Moreove
r, the inhibitory effects of each peptide on virus-induced cell fusion
were found to be virus type-specific. These peptides were found to al
so inhibit viral entry and to prevent plaque formation when mixed with
the virus inoculum. Furthermore, the peptides caused a reduction in v
irus yield when assayed 48 hr after low m.o.i. infection and in the si
ze of viral plaques when added to the overlay. Shorter peptides (21 a.
a. for P12F or 24 a.a. for P13F) which correspond to the partial seque
nce of heptad repeat a for P12F and the entire heptad repeat B for P13
F showed partial inhibition of P12- or P13-induced cell fusion. These
results indicate that peptides containing the heptad repeat a sequence
have the potential to inhibit virus-induced cell fusion, virus entry,
and spread of virus infection. (C) 1996 Academic Press, Inc.