Abstract
Vision begins in rods and cones with light detection by visual pigments in the membranes of the cells' outer segments, and the conversion of this initial quantum event into a series of highly amplified biochemical reactions leading to closure of channels in the outer segment plasma membrane and electrical hyperpolarization. The first stages are membrane-delimited activation of the G protein, transducin, and the cGMP phosphodiesterase, PDE6. The diffusible messenger cGMP carries the signal to cyclic nucleotide-gated channels in the plasma membrane, which close as [cGMP] decreases, leading to reduction in the dark current and hyperpolarization. Upon return to darkness, every step of activation is terminated or reversed, primarily through additional membrane-delimited reactions, with an important role played by Ca2+-feedback mechanisms, involving (the channels?), a Na+/Ca2+-K+ exchanger, and Ca2+-binding proteins. The outlines of this pathway are well established, but many quantitative and structural details remain to be determined.
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