Role of Gln114 in Spectral Tuning of a Long-Wavelength Sensitive Visual Pigment

Biochemistry ◽  
2019 ◽  
Vol 58 (26) ◽  
pp. 2944-2952 ◽  
Author(s):  
Kota Katayama ◽  
Shunta Nakamura ◽  
Takuma Sasaki ◽  
Hiroo Imai ◽  
Hideki Kandori
Keyword(s):  
Visual Pigment ◽  
Spectral Tuning ◽  
Long Wavelength

“In situ” observation of the role of chloride ion binding to monkey green sensitive visual pigment by ATR-FTIR spectroscopy

2018 ◽  
Vol 20 (5) ◽  
pp. 3381-3387 ◽  
Author(s):  
Kota Katayama ◽  
Yuji Furutani ◽  
Masayo Iwaki ◽  
Tetsuya Fukuda ◽  
Hiroo Imai ◽  
...  
Keyword(s):  
Spectroscopic Study ◽  
Ftir Spectroscopy ◽  
Visual Pigment ◽  
Chloride Ion ◽  
Ion Binding ◽  
In Situ Observation ◽  
The Novel ◽  
Long Wavelength

ATR-FTIR spectroscopic study elucidates the novel role of Cl−-binding in primate long-wavelength-sensitive (LWS) visual pigment.

scholarly journals Anesthetic state modulates excitability but not spectral tuning or neural discrimination in single auditory midbrain neurons

2011 ◽  
Vol 106 (2) ◽  
pp. 500-514 ◽  
Author(s):  
Joseph W. Schumacher ◽  
David M. Schneider ◽  
Sarah M. N. Woolley
Keyword(s):  
Receptive Fields ◽  
Population Level ◽  
Sensory Function ◽  
Spectral Tuning ◽  
Auditory Midbrain ◽  
Sensory Physiology ◽  
Neural Excitability ◽  
Midbrain Neurons ◽  
Spectrotemporal Receptive Fields

The majority of sensory physiology experiments have used anesthesia to facilitate the recording of neural activity. Current techniques allow researchers to study sensory function in the context of varying behavioral states. To reconcile results across multiple behavioral and anesthetic states, it is important to consider how and to what extent anesthesia plays a role in shaping neural response properties. The role of anesthesia has been the subject of much debate, but the extent to which sensory coding properties are altered by anesthesia has yet to be fully defined. In this study we asked how urethane, an anesthetic commonly used for avian and mammalian sensory physiology, affects the coding of complex communication vocalizations (songs) and simple artificial stimuli in the songbird auditory midbrain. We measured spontaneous and song-driven spike rates, spectrotemporal receptive fields, and neural discriminability from responses to songs in single auditory midbrain neurons. In the same neurons, we recorded responses to pure tone stimuli ranging in frequency and intensity. Finally, we assessed the effect of urethane on population-level representations of birdsong. Results showed that intrinsic neural excitability is significantly depressed by urethane but that spectral tuning, single neuron discriminability, and population representations of song do not differ significantly between unanesthetized and anesthetized animals.

Spectral absorbance, structure, and population density of photoreceptors in the retina of the lake sturgeon (Acipenser fulvescens)

2007 ◽  
Vol 85 (4) ◽  
pp. 584-587 ◽  
Author(s):  
A.J. Sillman ◽  
E.K. Ong ◽  
E.R. Loew
Keyword(s):  
Visual Pigment ◽  
Visual Pigments ◽  
Lake Sturgeon ◽  
Acipenser Fulvescens ◽  
Long Wavelength ◽  
Rods And Cones ◽  
The North ◽  
Spectral Absorbance ◽  
Dim Light ◽  
Scanning Electron

Lake sturgeon ( Acipenser fulvescens Rafinesque, 1817) photoreceptors were studied with scanning electron microscopy and microspectrophotometry. The retina contains both rods and cones, with cones estimated composing about 30% of the photoreceptor population. Only large single cones were identified and they are similar to those found in other species of the order Acipenseriformes. The rods are large, with long, broad outer segments, and are similar to the dominant rod found in other sturgeons and the North American paddlefish ( Polyodon spathula (Walbaum, 1792)). Mean (SD) rod packing density at 22 624 ± 3 509 rods/mm2 is low compared with those of other animals that function primarily in dim light. The visual pigment of the rods has a mean (SD) peak absorbance (λmax) at 541 ± 2 nm. Three different cone populations were identified: a long wavelength sensitive cone containing a visual pigment with λmax at 619 ± 3 nm; middle wavelength sensitive cone with λmax at 538 ± 1 nm; and short wavelength sensitive cone with λmax at 448 ± 1 nm. All the visual pigments are based on the vitamin A2 chromophore.

Visual pigments and oil droplets in diurnal lizards

2002 ◽  
Vol 205 (7) ◽  
pp. 927-938 ◽  
Author(s):  
Ellis R. Loew ◽  
Leo J. Fleishman ◽  
Russell G. Foster ◽  
Ignacio Provencio
Keyword(s):  
Visual Pigment ◽  
Visual Pigments ◽  
Anolis Carolinensis ◽  
Visual Cell ◽  
Oil Droplets ◽  
Oil Droplet ◽  
Long Wavelength ◽  
Apparent Color ◽  
Vitamin A2 ◽  
Insight Into

SUMMARY We report microspectrophotometric (MSP) data for the visual pigments and oil droplets of 17 species of Caribbean anoline lizard known to live in differing photic habitats and having distinctly different dewlap colors. The outgroup Polychrus marmoratus was also examined to gain insight into the ancestral condition. Except for Anolis carolinensis, which is known to use vitamin A2 as its visual pigment chromophore, all anoline species examined possessed at least four vitamin-A1-based visual pigments with maximum absorbance (λmax) at 564, 495,455 and 365 nm. To the previously reported visual pigments for A. carolinensis we add an ultraviolet-sensitive one withλ max at 365 nm. Five common classes of oil droplet were measured, named according to apparent color and associated with specific cone classes — yellow and green in long-wavelength-sensitive (LWS) cones,green only in medium-wavelength-sensitive (MWS) cones and colorless in short-wavelength-sensitive (SWS) and ultraviolet-sensitive (UVS) cones. MSP data showed that the colorless droplet in the SWS cone had significant absorption between 350 and 400 nm, while the colorless droplet in the UVS cone did not. The pattern for Polychrus marmoratus was identical to that for the anoles except for the presence of a previously undescribed visual cell with a rod-like outer segment, a visual pigment with a λmaxof 497 nm and a colorless oil droplet like that in the UVS cones. These findings suggest that anoline visual pigments, as far as they determine visual system spectral sensitivity, are not necessarily adapted to the photic environment or to the color of significant visual targets (e.g. dewlaps).

scholarly journals The role of retinal photoisomerase in the visual cycle of the honeybee.

1991 ◽  
Vol 97 (1) ◽  
pp. 143-165 ◽  
Author(s):  
W C Smith ◽  
T H Goldsmith
Keyword(s):  
Visual Pigment ◽  
Compound Eye ◽  
Rod Outer Segments ◽  
Visual Cycle ◽  
In Vitro Techniques ◽  
The Third ◽  
Isomerization Processes

The compound eye of the honeybee has previously been shown to contain a soluble retinal photoisomerase which, in vitro, is able to catalyze stereospecifically the photoconversion of all-trans retinal to 11-cis retinal. In this study we combine in vivo and in vitro techniques to demonstrate how the retinal photoisomerase is involved in the visual cycle, creating 11-cis retinal for the generation of visual pigment. Honeybees have approximately 2.5 pmol/eye of retinal associated with visual pigments, but larger amounts (4-12 pmol/eye) of both retinal and retinol bound to soluble proteins. When bees are dark adapted for 24 h or longer, greater than 80% of the endogenous retinal, mostly in the all-trans configuration, is associated with the retinal photoisomerase. On exposure to blue light the retinal is isomerized to 11-cis, which makes it available to an alcohol dehydrogenase. Most of it is then reduced to 11-cis retinol. The retinol is not esterified and remains associated with a soluble protein, serving as a reservoir of 11-cis retinoid available for renewal of visual pigment. Alternatively, 11-cis retinal can be transferred directly to opsin to regenerate rhodopsin, as shown by synthesis of rhodopsin in bleached frog rod outer segments. This retinaldehyde cycle from the honeybee is the third to be described. It appears very similar to the system in another group of arthropods, flies, and differs from the isomerization processes in vertebrates and cephalopod mollusks.

Molecular Basis of Spectral Tuning in the Newt Short Wavelength Sensitive Visual Pigment†

Biochemistry ◽  
2003 ◽  
Vol 42 (20) ◽  
pp. 6025-6034 ◽  
Author(s):  
Yusuke Takahashi ◽  
Thomas G. Ebrey
Keyword(s):  
Visual Pigment ◽  
Short Wavelength ◽  
Molecular Basis ◽  
Spectral Tuning

scholarly journals Turning Cones Off: the Role of the 9-Methyl Group of Retinal in Red Cones

2006 ◽  
Vol 128 (6) ◽  
pp. 671-685 ◽  
Author(s):  
Maureen E. Estevez ◽  
Petri Ala-Laurila ◽  
Rosalie K. Crouch ◽  
M. Carter Cornwall
Keyword(s):  
Visual Pigment ◽  
Bright Light ◽  
Rapid Rate ◽  
Methyl Group ◽  
Cone Opsin ◽  
Rate Of Recovery ◽  
Kinetics Of ◽  
Flash Response

Our ability to see in bright light depends critically on the rapid rate at which cone photoreceptors detect and adapt to changes in illumination. This is achieved, in part, by their rapid response termination. In this study, we investigate the hypothesis that this rapid termination of the response in red cones is dependent on interactions between the 9-methyl group of retinal and red cone opsin, which are required for timely metarhodopsin (Meta) II decay. We used single-cell electrical recordings of flash responses to assess the kinetics of response termination and to calculate guanylyl cyclase (GC) rates in salamander red cones containing native visual pigment as well as visual pigment regenerated with 11-cis 9-demethyl retinal, an analogue of retinal in which the 9-methyl group is missing. After exposure to bright light that photoactivated more than ∼0.2% of the pigment, red cones containing the analogue pigment had a slower recovery of both flash response amplitudes and GC rates (up to 10 times slower at high bleaches) than red cones containing 11-cis retinal. This finding is consistent with previously published biochemical data demonstrating that red cone opsin regenerated in vitro with 11-cis 9-demethyl retinal exhibited prolonged activation as a result of slowed Meta II decay. Our results suggest that two different mechanisms regulate the recovery of responsiveness in red cones after exposure to light. We propose a model in which the response recovery in red cones can be regulated (particularly at high light intensities) by the Meta II decay rate if that rate has been inhibited. In red cones, the interaction of the 9-methyl group of retinal with opsin promotes efficient Meta II decay and, thus, the rapid rate of recovery.

Suppression of cone-driven responses by rods in the isolated frog retina

1988 ◽  
Vol 1 (4) ◽  
pp. 331-338 ◽  
Author(s):  
Cun-Jian Dong ◽  
Hao-Hua Qian ◽  
John S. McReynolds ◽  
Xiong-Li Yang ◽  
Yu-Min Liu
Keyword(s):  
Dark Adaptation ◽  
Visual Pigment ◽  
Pigment Epithelium ◽  
Signal Transmission ◽  
Receptor Potential ◽  
Response Sensitivity ◽  
Long Wavelength ◽  
Negligible Amount ◽  
Frog Retina ◽  
Time Courses

AbstractThe sensitivity of rod- and cone-driven responses was studied in the isolated frog retina during the period of rapid dark adaptation following a conditioning flash which bleached a negligible amount of visual pigment. Following a conditioning flash, cone-driven b-wave responses were first enhanced and then depressed. The time courses of the enhancement and subsequent depression of cone-drive responses varies greatly with the intensity and wavelength of the conditioning flash, but were identical when the conditioning' flashes were matched for equal excitation of 502 nm rods. These changes in cone-driven response sensitivity were correlated with the desensitization and recovery of rods following the conditioning flash. When signal transmission from rods to second-order cells was interrupted by the addition of L-glutamate, the conditioning flash did not produce the above-described enhancement and subsequent depression of long-wavelength receptor potential responses. The suppression of cone-driven response therefore appears to be due to a synaptically mediated influence from 502 nm rods which is maximal when the rods are in the dark-adapted state, with little or no contribution from 433 nm rods, and no involvement of the pigment epithelium.

Spectral-tuning mechanisms of marine mammal rhodopsins and correlations with foraging depth

2000 ◽  
Vol 17 (5) ◽  
pp. 781-788 ◽  
Author(s):  
JEFFRY I. FASICK ◽  
PHYLLIS R. ROBINSON
Keyword(s):  
Amino Acid ◽  
Marine Mammal ◽  
Molecular Basis ◽  
Marine Mammals ◽  
Visual Pigments ◽  
Amino Acid Substitutions ◽  
Spectral Tuning ◽  
Long Wavelength ◽  
Terrestrial Mammals ◽  
Deep Diving

It has been observed that deep-foraging marine mammals have visual pigments that are blue shifted in terms of their wavelength of maximal absorbance (λmax) when compared to analogous pigments from terrestrial mammals. The mechanisms underlying the spectral tuning of two of these blue-shifted pigments have recently been elucidated and depend on three amino acid substitutions (83Asn, 292Ser, and 299Ser) in dolphin rhodopsin, but only one amino acid substitution (308Ser) in the dolphin long-wavelength-sensitive pigment. The objective of this study was to investigate the molecular basis for changes in the spectral sensitivity of rod visual pigments from seven distantly related marine mammals. The results show a relationship between blue-shifted rhodopsins (λmax ≤ 490 nm), deep-diving foraging behavior, and the substitutions 83Asn and 292Ser. Species that forage primarily near the surface in coastal habitats have a rhodopsin with a λmax similar to that of terrestrial mammals (500 nm) and possess the substitutions 83Asp and 292Ala, identical to rhodopsins from terrestrial mammals.

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