The research interests of my lab focus on the fundamental biological problems of vesicle mobilization and membrane fusion. In the nervous system, where the strength of the neurosecretory process is critical for learning and memory, synaptic vesicle mobilization and fusion are regulated in dynamic ways. We are studying neurosecretion at the crusteacean neuromuscular junction, where synaptic output is exquisitely regulated both by the frequency of electrical activity in the motoneuron and by the modulatory effects of circulating neurohormones. At this synapse, the number of synaptic vesicles that undergo exocytosis in response to a single action potential is a steep function of the stimulus frequency. This phenomenon is called frequency facilitation, and is a form of short-term synaptic plasticity. By electrophysiologically measuring synaptic output from a small number of release sites during frequency facilitation, we have developed a quantitative model that describes synaptic transmission in terms of the mobilization of synaptic vesicles to dock at release sites (Worden et al., 1997).The utility of the stimulus-dependent mobilization model is that it enables estimation of the number of quantal units of transmitter mobilized by each action potential, as well as the rate constant of quantal demobilization from the docking sites back to the reserve quantal store. One current line of research focuses on the cellular mechanisms by which circulating hormones, such as serotonin, potentiate neurotransmission. We are testing the hypothesis that serotonin either enhances quantal mobilization or decreases quantal demobilization, in addition to increasing the probability of quantal fusion. Future plans include examining how second messenger pathways regulate the processes of quantal mobilization and docking, and identifying the physiological roles played by synaptic proteins in the neurosecretory process.