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Photoreceptor guanylate cyclase variants: cGMP production under control.
Author(s) -
Izabela Sokal,
Andrei Alekseev,
Krzysztof Palczewski
Publication year - 2003
Publication title -
acta biochimica polonica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.452
H-Index - 78
eISSN - 1734-154X
pISSN - 0001-527X
DOI - 10.18388/abp.2003_3633
Subject(s) - visual phototransduction , phosphodiesterase , guanylate cyclase , rhodopsin , second messenger system , microbiology and biotechnology , chemistry , stimulation , biophysics , gucy1b3 , biochemistry , signal transduction , cyclic gmp , biology , enzyme , guanylate cyclase 2c , neuroscience , retinal
Changes in the Ca2+ concentration are thought to affect many processes, including signal transduction in a vast number of biological systems. However, only in few cases the molecular mechanisms by which Ca2+ mediates its action are as well understood as in phototransduction. In dark-adapted photoreceptor cells, the equilibrium level of cGMP is maintained by two opposing activities, such as phosphodiesterase (PDE) and guanylate cyclase (GC). Upon absorption of photons, rhodopsin-G-protein-mediated activation of PDE leads to a transient decrease in [cGMP] and subsequently to lowering of [Ca2+]. In turn, lower [Ca2+] increases net production of cGMP by stimulation of GC until dark conditions are re-established. This activation of GC is mediated by Ca2+ -free forms of Ca2+ -binding proteins termed GC-activating proteins (GCAPs). The last decade brought the molecular identification of GCs and GCAPs in the visual system. Recent efforts have been directed toward understanding the properties of GC at the physiological and structural levels. Here, we summarize the recent progress and present a list of topics of ongoing research.

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