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Query: UMLS:C0027960 (mole)
 21,279 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

1. The hydrolysis of guanosine triphosphate (GTP) and the consequent formation of guanosine diphosphate (GDP) and phosphate (P1) are activated by light in a suspension of broken retinal rods: the hydrolysis rate with GTP in the micrometer concentration range is 2.5-3.5 n-mole/min per mg of rhodopsin in the preparation. 2. The ionic composition of the medium suspending the rods is not critical: the hydrolysis is present in NaCl saline solution with MG2+ as well as in Tris-HC1 buffer solution, and with the chelating agent EDTA. 3. The ionic strength is critical: the effect is reduced when the broken rods are suspended in a low salt mannitol solution, and is altogether abolished when they are separated from the mannitol solution; it reappears when the mannitol solution is added again in the presence of salts. An element essential for the effect is thus reversibly released in the mannitol solution. No hydrolytic activity on GTP, however, is found in the mannitol soluble fraction. 4. The cyclic nucleotide phosphodiesterase is eluted from the rods in the mannitol solution, and is reaggregated to the rods in the presence of salts; once recombined with the rods, it can be activated by light. 5. The activation of the phosphodiesterase by light is present in the absence of added nucleotide triphosphates.
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PMID:Light-activated hydrolysis of GTP and cyclic GMP in the rod outer segments. 20 80

The microviscosity of rhodopsin boundary lipids was studied with a spin-labeled fatty acid covalently attached to rhodopsin, in rhodopsin-egg lecithin vesicles. When the lipid-to-protein ratio was high (500:1, mole to mole), only narrow peaks were visible in electron paramagnetic resonance spectrum at 37 degrees C. This enabled us to show that, under these conditions, not more than 10% of the probes have their motion strongly restricted by the proximity of the protein. When the temperature was reduced, a second component characteristic of strong immobilization appeared. It corresponds to 50% of the signal at -5 degrees C. At all temperatures reduction of the lipid-to-protein ratio also resulted in an increase of the amount of immobilized lipid. These results show that the rhodopsin boundary layer under physiological conditions is associated with low microviscosity. However, low temperatures, low lipid-to-protein ratios, or combinations of the two can induce dramatic modifications of the physical state of the boundary lipids, which under these conditions may no longer be representative of the functional biological system. These results are relevant to the general theory of lipid-protein interaction.
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PMID:Physical modifications of rhodopsin boundary lipids in lecithin-rhodopsin complexes: a spin-label study. 22 56

The kinetics of photoinduced changes of protein fluorescence of cattle visual pigment was studied in the presence of hydroxylamine. The rate constant of fluorescence increase is proportional to NH2OH concentration when it is less than 0.4 M. It reaches the maximal magnitude (3.3 +/- 1 sec-1) at higher hydroxylamine concentration. Fluorescence increase rate is controlled by the rate of chemical reaction of rhodopsin with hydroxylamine. It is limited by conformational rearrangement of opsin. This rearrangement does not induce absorbance spectrum change of visual pigment, but confers to it the capability to react with NH2OH and NaBH4. Kinetic parameters of this rearrangement (tau 20 degrees C approximately 300 msec, Eact = 19 +/- 2 kcal/mole) coincide with kinetic parameters of diminishing of the photoresponse of artificial lipid membrane modified by fragments of rod outer segments in the temperature range studied (+2 divided by +25 degrees C).
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PMID:[Molecular mechanisms of receptor-potential generation by the photoreceptor. III. Conformational transition responsible for the tail end of the photoresponse of an artificial lipid membrane modified by fragments of the external segments of rods]. 61 34

1. The high energy phosphate esters available for the luminescent reaction of the firefly lantern extract correspond, in the dark adapted rods of the frog, to 7 X 10(-16) mole of ATP per rod, corresponding to ca. 1-4 mM. 2. Rods isolated from light adapted eyes contain a smaller amount. 3. The high energy phosphate esters are reduced spontaneously at a rate of 50% in 24 min, in the isolated rods in darkness. 4. Bleaching a few per cent of the rhodopsin molecules of a rod suspension induces a 60% decrease achieved in less than 12 sec. 5. The ionophore A23187 decreases the high energy phosphate esters when the extracellular free Ca concentration is greater than 10(-7) M, suggesting that ATP is consumed in pumping Ca ions out of the rods, or into the disks contained in the rods, or both.
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PMID:On the metabolism of the rod outer segments. 78 Dec 15

32P-rhodopsin was partially separated by isoelectric focusing into several fractions of different phosphorylation extent. It was found that the incorporated phosphate is not uniformly distributed in a population of rhodopsin molecules. In a preparation with an average phosphorylation extent of 2.4 moles of phosphate per mole of rhodopsin, most of the 32P-phosphate was found in fractions where 4-5 phosphates are bound per rhodopsin, whereas a large fraction of the total rhodopsin was not phosphorylated at all. The maximum number os phosphate binding sites in rhodopsin appears to be at least five.
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PMID:Isoelectric focusing of phosphorylated cattle rhodopsin. 89 58

The effect of illumination on the calcium (Ca) translocation mechanisms in isolated frog rod outer segments (ROS) was studied. The ATP-dependent Ca uptake and the Ca-Ca exchange mechanisms were unaffected by light. In contrast, we report a light-evoked Ca efflux which is mediated by the Na-Ca exchange system. The ratio of released Ca to rhodopsin bleaching was measured and the stoichiometry obtained was 5 Ca molecules released per mole of rhodopsin bleached. Concomitant to the Ca release, light induced Ca uptake, which increase the total Ca content of ROS. Physiological relevance of results to the phototransduction process is discussed.
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PMID:Effect of light on Na-Ca exchange in rod outer segments in frog. 258 Nov 88

Rhodopsin in rod outer segment disk membranes was enzymatically modified by erythrocyte transglutaminase, which linked small primary amines to glutamine residues. In order to avoid formation of protein crosslinks, rhodopsin was first reductively methylated to modify its lysines. From 1.9 to 2.5 mol of putrescine, ethanolamine, or dinitrophenylcadaverine were incorporated into rhodopsin by transglutaminase during 16 h reaction time. A maximum of 3.5 mol of [14C]putrescine was incorporated per mole of rhodopsin during 48 h. Essentially all of the rhodopsin sequence containing the putrescine could be removed by limited proteolysis of the membranes by thermolysin. Glutamine residues in positions 236, 237, 238, and 344 were modified to approximately equal extents, as determined by isolation of the cyanogen bromide peptides of modified rhodopsin followed by further subdigestion of the peptides. The modified glutamine residues are located in the helix V-VI (or F1-F2) connecting loop and in the carboxyl-terminal region of rhodopsin.
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PMID:Transglutaminase modification of rhodopsin in retinal rod outer segment disk membranes. 287 89

The thermostability of visual pigments in bovine, rat and frog rod outer segments (ROS) has been studied by means of differential scanning calorimetry and thermal gel analysis methods. Use of the two different methods has allowed to assign calorimetric peaks to rhodopsin and opsin denaturation. The denaturation enthalpy changes for rhodopsin in bovine, rat and frog ROS are 630 kJ/mole (Td = 347 degrees C), 416 kJ/mole (Td = 340 degrees K) and 410 kJ/mole (Td = 340 degrees K), respectively. Corresponding values for opsins are 490 kJ/mole (Td = 332 degrees K), 269 kJ/mole (Td = 320 degrees K) and 158 kJ/mole (Td = 319 degrees K). The free energy of stabilization of the rhodopsin native structure is not very large and practically similar to that for native water soluble globular proteins.
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PMID:Calorimetric study of thermal denaturation of vertebrate visual pigments. 326 68

Albino rats were born and raised through 12 weeks of age in 12L:12D regimes of 5, 300- or 800-lx illuminance. Upon killing, the animals' retinas were examined for the following: (1) rhodopsin of whole retina and isolated rod outer-segment membrane; (2) retinal morphology, including outer segment length and outer nuclear layer area; and (3) outer-segment membrane lipid biochemistry. The three groups of animals show significant differences with respect to one another for nearly every parameter measured. Rod outer-segment membranes of rats raised in dim cyclic light (5 lx) have high rhodopsin packing densities, high levels of polyunsaturated fatty acids, and low cholesterol levels in comparison with animals raised in brighter illuminances (300- or 800 lx). The mole ratio of phospholipid to rhodopsin in the outer-segment membrane of rats raised in 5-lx cyclic light is only 43% of that of rats raised in 800-lx cyclic light. The difference between these two groups of animals for docosahexaenoic acid is greater than three times, with dim light-reared animals showing higher levels. These rats (5 lx-reared) have less cholesterol in their photoreceptor outer segments, 6.6 mol% compared with 19.7 mol% for animals from the 800-lx regime. In all cases, rats from the intermediate rearing illuminance (300 lx) exhibit intermediate membrane composition values. It is likely that these differences in membrane composition illustrate a profound effect of light history on photoreceptor function.
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PMID:Effect of light history on rod outer-segment membrane composition in the rat. 365 72

Biochemical and immunological techniques were used to determine the emergence of interstitial retinol binding protein (IRBP), rhodopsin, and stored retinyl esters (all-trans and 11-cis) during retinal development in normal and rd mice. IRBP could be demonstrated at embryonic Day 17 (E17), corresponding to an early stage of inner segment development. Although all-trans retinyl esters were present earlier, 11-cis retinyl esters did not appear until postnatal Days 6-7 (P6-P7), corresponding to rod outer segment (ROS) disc formation. Rhodopsin was detected at the same developmental stage. The proportion of 11-cis retinyl esters reached a maximum of 40-50% at P15-P20. Thereafter, the proportion dropped, due to more rapid accumulation of the all-trans isomer. Rhodopsin and IRBP increased in parallel with ROS elongation up to P25, when the ROS had reached their mature lengths. The increases then continued up to P40-P50. In rd (retinal degeneration) mice, IRBP and rhodopsin were identical with the controls until P12, but then dropped as the photoreceptors degenerated. Synthesis and secretion of IRBP in vitro was less than 10% of the controls in rd retinas at P26, when only 4-5% of the photoreceptors survived. The quantities of retinyl esters (mainly stearate and palmitate in the ratio of 6:1, respectively) stored in dark-adapted mouse eyes progressively increased as the animals aged, representing 0.5 mole eq. of the rhodopsin at 8 months. Although retinyl esters (11-cis and all-trans) also accumulated in rd mouse eyes up to P12, little further increase occurred. At P93, the retinyl esters (0.01 nmole X eye-1) were only 4% of the controls at P91. A peak in the proportion of 11-cis isomer occurred at P10-P20, but it averaged only 15% of the total ester and declined to 5% at P93. These findings support the hypothesis that IRBP is synthesized by the rods and cones, and suggest that its synthesis and secretion are initiated when the photoreceptor inner segments start to differentiate. 11-cis Retinoids and rhodopsin do not appear until the outer segments start to form. It is suggested that in the rd mouse the absence of photoreceptors, perhaps coupled with lack of normal interphotoreceptor matrix, leads to a loss in the ability of the pigment epithelium to store retinyl esters.
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PMID:Rhodopsin, 11-cis vitamin A, and interstitial retinol-binding protein (IRBP) during retinal development in normal and rd mutant mice. 373 15


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