Individual phospholipid vesicles, 1 to 5 micrometers in diameter, containin
g a single reagent or a complete reaction system, were immobilized with an
infrared laser optical trap or by adhesion to modified borosilicate glass s
urfaces. Chemical transformations were initiated either by electroporation
or by electrofusion, in each case through application of a short (10-micros
econd), intense (20 to 50 kilovolts per centimeter) electric pulse delivere
d across ultramicroelectrodes. Product formation was monitored by far-field
laser fluorescence microscopy. The ultrasmall characteristic of this react
ion volume led to rapid diffusional mixing that permits the study of fast c
hemical kinetics. This technique is also well suited for the study of react
ion dynamics of biological molecules within lipid-enclosed nanoenvironments
that mimic cell membranes.