Cell-attached capacitance measurements were used to detect unitary exo
cytotic and endocytotic events in protoplasts from Zea mays L. coleopt
iles with a high-frequency lock-in amplifier. A background noise level
of around 70 aF permitted the detection of interacting vesicles with
a diameter as small as 60 nm. The distribution of discrete on-steps (e
xocytosis) was similar to that of off-steps (endocytosis) with a modal
values at about 200 aF for both events. From the frequency of endocyt
otic events (1.5 +/- 1.4 min(-1)) it is estimated that 200 min are req
uired for the whole membrane to be ingested in a non-stimulated protop
last.