Cyclic guanosine monophosphate, usually abbreviated cGMP in physiological contexts, is a nucleotide whose phosphate links the 3′ and 5′ positions of its ribose in an intramolecular ring. It acts as a second messenger: changes in its concentration connect upstream activity to downstream targets. Its cyclic phosphate arrangement distinguishes it from ordinary linear guanosine monophosphate.
Guanylate cyclase produces cGMP from guanosine triphosphate, while a suitable phosphodiesterase hydrolyzes the cyclic linkage. The number of phosphate groups is not the central distinction between cyclic and linear GMP: both names describe one phosphate, with different bonding arrangements.
A classic experiment tested how this messenger affects a membrane directly. In excised inside-out patches from rod outer-segment membranes, cGMP applied to the inner face reversibly increased cationic conductance. The effect occurred without nucleoside triphosphates, arguing against mediation by protein phosphorylation in that assay. Cyclic AMP and 2′,3′-cyclic GMP did not reproduce the response under the reported tests.[ref]
Induction by cyclic GMP of cationic conductance in plasma membrane of retinal rod outer segment by E. E. Fesenko and others. 1985 abstract: excised patches, reversible conductance, nucleotide controls and absence of triphosphates.
The result makes molecular recognition concrete: related cyclic nucleotides are not automatically interchangeable. In the visual pathway, activated transducin can stimulate downstream phosphodiesterase activity, connecting rhodopsin activation with a change in the messenger system.[ref]
Flow of information in the light-triggered cyclic nucleotide cascade of vision by B. K. Fung and others. Reconstitution and activated alpha-subunit stimulation of phosphodiesterase.
A concentration measurement and a channel response nevertheless answer different questions. To interpret a signaling experiment, specify the compartment, time and target; a single whole-cell average need not capture the concentration experienced by every molecular partner.
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