RAPID calcium-dependent exocytosis underlies neurotransmitter release
from nerve terminals. Despite the fundamental importance of this proce
ss, neither the relationship between presynaptic intracellular calcium
ion concentration ([Ca2+](i)) and rate of exocytosis, nor the maximal
rate of secretion is known quantitatively. To provide this informatio
n, we have used flash photolysis of caged Ca2+ to elevate [Ca2+](i) ra
pidly and uniformly in synaptic terminals, while measuring membrane ca
pacitance as ao index of exocytosis and monitoring [Ca2+](i) with a Ca
2+-indicator dye. When [Ca2+](i) was abruptly increased to > 10 mu M,
capacitance rose at a rate that increased steeply with [Ca2+](i). The
steepness suggested that at least four calcium ions must bind to activ
ate synaptic vesicle fusion. Half-saturation was at 194 mu M, and the
maximal rate constant was 2,000-3,000 s(-1). A given synaptic vesicle
can exocytose with high probability within a few hundred microseconds,
if [Ca2+](i) rises above 100 mu M These properties provide for the ex
tremely rapid signalling required for neuronal communication.