New sampling protocols combined with matrix-assisted laser desorption/ioniz
ation time-of-flight mass spectrometry (MALDI-TOF MS) allow the assay of si
ngle dense core vesicles. Understanding the packaging of vesicles is import
ant as vesicles are the quanta of information for intercellular communicati
on. Using vesicles from the exocrine atrial gland of Aplysia californica as
the model, a wide range of bioactive peptides are detected within each ves
icle. Although the expression of the egg-laying hormone gene family of type
1 atrial gland cells has been previously examined, chemical characterizati
on of individual 1-2 mu m diameter vesicles demonstrates that products from
several genes are colocalized. The mass sensitivity of MALDI MS can be fur
ther improved to enable the analysis of even smaller subcellular organelles
.