Recent structural studies of proteins mediating membrane fusion reveal intr
iguing similarities between diverse viral and mammalian systems. Particular
ly striking is the close similarity between the transmembrane envelope glyc
oproteins from the retrovirus HTLV-1 and the filovirus Ebola. These similar
ities suggest similar mechanisms of membrane fusion. The model that fits mo
st currently available data suggests fusion activation in viral systems is
driven by a symmetrical conformational change triggered by an activation ev
ent such as receptor binding or a pH change. The mammalian vesicle fusion m
ediated by the SNARE protein complex most likely occurs by a similar mechan
ism but without symmetry constraints.