Thermal activation of the visual pigment constitutes a fundamental constraint on visual sensitivity.
Its electrical correlate in the membrane current of dark-adapted rods are randomly occurring
discrete ‘dark events’ indistinguishable from responses to single photons. It has been proposed that
thermal activation occurs in a small subpopulation of rhodopsin molecules where the Schiff base
linking the chromophore to the protein part is unprotonated. On this hypothesis, rates of thermal
activation should increase strongly with rising pH. The hypothesis has been tested by measuring the
effect of pH changes on the frequency of discrete dark events in red rods of the common toad Bufo
bufo. Dark noise was recorded from isolated rods using the suction pipette technique. Changes in
cytoplasmic pH upon manipulations of extracellular pH were quantified by measuring, using
fast single-cell microspectrophotometry, the pH-dependent metarhodopsin I–metarhodopsin II
equilibrium and subsequent metarhodopsin III formation. These measurements show that, in the
conditions of the electrophysiological experiments, changing perfusion pH from 6.5 to 9.3 resulted
in a cytoplasmic pH shift from 7.6 to 8.5 that was readily sensed by the rhodopsin. This shift, which
implies an 8-fold decrease in cytoplasmic [H+], did not increase the rate of dark events. The results
contradict the hypothesis that thermal pigment activation depends on prior deprotonation of the
Schiff base
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