Above: Schematic of cell-flow flash photolysis set-up for measurement of agonist-induced currents in the millisecond time-scale. Left: The whole-cell current recorded after flash photolysis of a "caged" acetylcholine analog equilibrated with the nicotinic acetylcholine receptors on the surface of the clonal mammlian BC3H1 muscle cell. |
Geetha, N. and Hess, G.P. On the mechanism of a mammalian g-aminobutyric acid receptor in primary brain cells. Chemical kinetic measurements with a 10-millisecond time resolution. Biochemistry 31: 5488-5499 (1992).
Matsubara, N., Billington, A.P. and Hess, G.P. Laser-pulse photolysis of caged carbamoylcholine in investigations of a mammalian nicotinic acetylcholine receptor in BC3H1 cells: What can one learn from chemical kinetic measurements in the microsecond time region? Biochemistry 31: 5507-5514 (1992).
Hess, G.P. Determination of the chemical mechanism of neurotransmitter receptor-mediated reactions by rapid chemical kinetic techniques. Biochemistry 32: 989-1000 (1993).
Niu, L. and Hess, G.P. An acetylcholine receptor regulatory site in BC3 H1 cells: Characterized by laser-pulse photolysis in the microsecond-to-millisecond time domain. Biochemistry 32: 3831-3835 (1993).
Ramesh, D., Wieboldt, R., Niu, L., Carpenter, B.K. and Hess, G.P. Photolysis of a new protecting group for the carboxyl function of neurotransmitters within 3 microseconds and with product quantum yield of 0.2. Proc. Natl. Acad. Sci. USA 90: 11074-11078 (1993).