Abstract
A light-activated GTPase that functions as a component of the rhodopsin-linked, light-activated phosphodiesterase (PDEase) system in vertebrate photoreceptors has been reported. In our efforts to purify photoreceptor GTPase we encountered another component (which we call "helper" or "H" component) whose presence is required for expression of light-activated GTPase activity. We report here the characterization of this heat-labile, macromolecular factor and that the presence of helper is absolutely required for light- and rhodopsin-dependent activation of photoreceptor GTPase. Of equal importance, we find that the "G" component (which requires the presence of H for expression of GTPase activity) can bind GTP and can support light- and GTP-dependent PDEase activation in the absence of H component. These data support a model in which GTP binding to G component is a necessary condition for PDEase activation. Hydrolysis of GTP at the G activator locus (an H-dependent activity) is a regulatory event which reverses PDEase activation. The complexity of this regulatory mechanism provides opportunities for signal modulation and amplification.
MeSH Terms
3',5'-Cyclic-GMP Phosphodiesterases/metabolism
Animals
Binding Sites
Cattle
Enzyme Activation
GTP Phosphohydrolases/metabolism,radiation effects
Guanosine Triphosphate/metabolism
Light
Membrane Proteins/metabolism
Molecular Weight
Phosphoric Monoester Hydrolases/metabolism
Photoreceptor Cells/enzymology
Proteins/metabolism
Rhodopsin/metabolism
Chemicals
Membrane Proteins
Proteins
Guanosine Triphosphate
Rhodopsin
Phosphoric Monoester Hydrolases
3',5'-Cyclic-GMP Phosphodiesterases
GTP Phosphohydrolases
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Shinozawa T
Uchida S
Martin E
Cafiso D
Hubbell W
Bitensky M
References (14)
14 references, click to expand
-
A second ouabain-sensitive sodium-dependent adenosine triphosphate in brain microsomes.
J Biol Chem. 1969 Dec 10;244(23):6493-7
PMID: 4242925
-
Preparation and properties of phospholipid bilayers containing rhodopsin.
Proc Natl Acad Sci U S A. 1972 Sep;69(9):2617-21
PMID: 4341702
-
The isolation of bacterial membrane ATPase and nectin.
Methods Enzymol. 1974;32:428-39
PMID: 4280489
-
Activation of photoreceptor disk membrane phosphodiesterase by light and ATP.
Adv Cyclic Nucleotide Res. 1975;5:213-40
PMID: 165667
-
A link between rhodopsin and disc membrane cyclic nucleotide phosphodiesterase. Action spectrum and sensitivity to illumination.
Biochemistry. 1975 Jun 17;14(12):2760-6
PMID: 167806
-
Purification and properties of the light-activated cyclic nucleotide phosphodiesterase of rod outer segments.
J Biol Chem. 1975 Aug 25;250(16):6320-7
PMID: 169236
-
Catecholamine-stimulated GTPase activity in turkey erythrocyte membranes.
Biochim Biophys Acta. 1976 Dec 8;452(2):538-51
PMID: 188466
-
Light-activated GTPase in vertebrate photoreceptors.
Nature. 1977 Oct 27;269(5631):822-4
PMID: 200847
-
A light-activated GTPase in vertebrate photoreceptors: regulation of light-activated cyclic GMP phosphodiesterase.
Proc Natl Acad Sci U S A. 1977 Oct;74(10):4238-42
PMID: 200909
-
The regulatory GTPase cycle of turkey erythrocyte adenylate cyclase.
J Cyclic Nucleotide Res. 1977 Dec;3(6):393-406
PMID: 203612
-
Light- and GTP-activated photoreceptor phosphodiesterase: regulation by a light-activated GTPase and identification of rhodopsin as the phosphodiesterase binding site.
Adv Cyclic Nucleotide Res. 1978;9:553-72
PMID: 27082
-
Predictive value of the analogy between hormone-sensitive adenylate cyclase and light-sensitive photoreceptor cyclic GMP phosphodiesterase: a specific role for a light-sensitive GTPase as a component in the activation sequence.
J Supramol Struct. 1979;10(2):185-90
PMID: 222967
-
Light-regulated enzymes of vertebrate retinal rods.
Adv Cyclic Nucleotide Res. 1979;11:265-301
PMID: 227247
-
A method for determining the sedimentation behavior of enzymes: application to protein mixtures.
J Biol Chem. 1961 May;236:1372-9
PMID: 13767412