Molecular mechanisms underlying the high temporal resolution of photoreceptors.
Molecular mechanisms underlying the high temporal resolution of photoreceptors.
批准号:
07458169
负责人:
HAYASHI Fumio
金额:
$4.74万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
1995
资助国家:
日本
项目状态:
已结题
起止时间:
1995 至 1996
中文摘要
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英文摘要
Photo-electric transduction system in photoreceptor cells of higher animals possesses sophisticated characteristics. First is the ability for adaptation against an extraordinarily wide back-ground illumination, and second is a high temporal resolution that allows the system to receipt a photic pulse as a pulse. PI examined the function of an inhibitory subunit of cGMP-phosphodiesterase (g subunit of PDE ; Pg) and its regulatory mechanism to elucidate the molecular mechanism that attributes to the high temporal resolution of photoreceptors. In addition, on the basis of the finding that inositol phospholipids affect the phosphorylation of Pg by an endogenous protein kinase in photoreceptors, PI examined the relationship between the regulatory mechanism of light-dependent cGMP phosphodiesterase and inositol phospholipids metabolizing system in rod photoreceptors.As for the endogenous protein kinase of Pg in rod photoreceptors, its molecular weight was found to be approximately 42-45 kDa and pI value was 5.2. PI could not succeed to obtain its specific antibody nor a clone of its gene for its low content in source organ, though PI obtained new insight in the function of Pg during the examination described above. By this time, the inhibition of the apo-enzyme of phosphodiesterase is the only one function of Pg. However, it was shown that the release of Pg from Pab by binding with transducin results in the release of cGMP from the non catalytic binding site on Pab. This fact suggests that the quick recovery of cGMP after light stimulation of PDE is at least partly attributable to the release of cGMP from Pab. Furthermore, PI found that the inhibitors of inositol phospholipid metabolism (U73122 and neomycin) significantly inhibit light-mediated cGMP hydrolysis in rod photoreceptor outer segments.
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TANAKA, H.: "MEKA/phosducin affenuates hydrophobicity of transduc in βγ subunits without binding to farnesyl moiety." Biochem. Biophys. Res. Commun.223. 587-591 (1996)
TANAKA, H.:“MEKA/phosducin 增强 βγ 亚基的疏水性,但不与法尼基部分结合。Biochem.Res.223。”
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Yamazaki,A.: "Possible Stimulation of retinal rod recovery to dark state by cGMP release from a cGMP phosphodiesterase noncatalytic site." J.Biol.Chem.271. 32495-32498 (1996)
Yamazaki,A.:“cGMP 磷酸二酯酶非催化位点释放 cGMP 可能刺激视网膜杆恢复至黑暗状态。”
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V.A.Bondarenko, M.Desai, S.Dua, M.Yamazaki, R.H.Amin, T.Kinumi, M.Ohashi, N.Komori, H.Matsumoto, K.W.Jackson, F.Hayashi, J.Usukura, V.M.Lipking, A.Yamazaki.: "Residues within the polycationic region of cGMP phosphodiesterase gamma sabunit crucial for the
V.A.Bondarenko、M.Desai、S.Dua、M.Yamazaki、R.H.Amin、T.Kinumi、M.Ohashi、N.Komori、H.Matsumoto、K.W.Jackson、F.Hayashi、J.Usukura、V.M.Lipking、A.
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林 文夫: "生物物理から見た生命像-感覚情報-" 吉岡書店(印刷中), (1997)
林文雄:“从生物物理学中看到的生命形象 - 感官信息 -”吉冈书店(正在出版),(1997)
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BONDARENKO,V.A.: "Residues within the polycationic region of cGMP phosphodiesterase γ subunit crucial for the interaction with transducin α subunit." J.Biol.Chem.(in press). (1997)
BONDArenKO, V.A.:“cGMP 磷酸二酯酶 γ 亚基的聚阳离子区域内的残基对于与转导蛋白 α 亚基的相互作用至关重要。”(出版中)。
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