Synaptosomes incorporated mixed brain gangliosides at a rapid initial
rate followed by a slower phase of net movement from the protein-assoc
iated fraction into the membrane core. The pattern of incorporated gan
gliosides reflected the pattern available for incorporation. Intact sy
naptosomes incorporated similar to 100 pmol GM1/mg protein. Synaptosom
es preincubated with proteolytic enzymes (trypsin, chymotrypsin, and p
apain) at different pH values (6.2, 7.4, 7.8) incorporated more exogen
ous gangliosides than synaptosomes preincubated in buffer alone. This
effect was maximal at pH 7.8, though analysis of variance revealed tha
t the proteolytic treatment and pH effects were probably independent p
rocesses. Overall uptake of exogenous gangliosides correlated signific
antly with amount of membrane protein loss, indicating that initial ac
cess of exogenous gangliosides to synaptosomal membranes is retarded b
y cell-surface proteins. These results suggest synaptosomes as a usefu
l alternative to cultured cells for investigating the interaction of g
angliosides with other cell surface constituents.