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蟾蜍光感受器中环状鸟苷单磷酸代谢的调节。对维持光激发和衰减状态的代谢事件的定义。

Regulation of cyclic GMP metabolism in toad photoreceptors. Definition of the metabolic events subserving photoexcited and attenuated states.

作者信息

Dawis S M, Graeff R M, Heyman R A, Walseth T F, Goldberg N D

机构信息

Department of Biochemistry, University of Minnesota Medical School, Minneapolis 55455.

出版信息

J Biol Chem. 1988 Jun 25;263(18):8771-85.

PMID:2837463
Abstract

Photoreceptor metabolism of cGMP and its regulation were characterized in isolated toad retinas by determining the intensity and time dependence of light-induced changes in the following metabolic parameters: cGMP hydrolytic flux determined by the rate of 18O incorporation from 18O-water into retinal guanine nucleotide alpha-phosphoryls; changes in the total (protein-bound and unbound) concentrations of the guanine nucleotide metabolic intermediates; and changes in the concentration of metabolic (unbound) GDP calculated from the fraction of the alpha-GDP that undergoes labeling with 18O. The latter is interpreted to reflect the state of the equilibrium between GDP- and GTP-complexed forms of G-protein. With narrow band 500 nm light that preferentially stimulates red rod photoreceptors, a range of intensities covering approximately 5 log units produced increases of over 10-fold in cGMP metabolic flux. However, the characteristics of the cGMP metabolic response over the first 2.5 log units of intensity are readily distinguishable from those at higher intensities which exhibit progressive attenuation by an intensity- and time-dependent process. Over the range of low intensities (0.6-3 log photons.micron-2.s-1) the metabolic response is characterized by 1) increases in cGMP hydrolytic flux of up to 8-fold as a logarithmic function of intensity of photic stimulation that are sustained for at least 200 s; 2) small increases or no change in the concentration of total cGMP; 3) large increases of up to 10-fold in the concentration of metabolically active GDP as a linear function of intensity with no significant change in the tissue concentrations of total GDP or GTP; and 4) amplification of the photosignal by the metabolism of approximately 10,000 molecules of cGMP per photoisomerization with the major site of amplification at the level of the interaction of bleached rhodopsin with G-protein.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过测定以下代谢参数中光诱导变化的强度和时间依赖性,对分离的蟾蜍视网膜中cGMP的光感受器代谢及其调节进行了表征:由18O-水掺入视网膜鸟嘌呤核苷酸α-磷酸的速率所确定的cGMP水解通量;鸟嘌呤核苷酸代谢中间体的总(蛋白质结合和未结合)浓度的变化;以及根据经历18O标记的α-GDP部分计算出的代谢(未结合)GDP浓度的变化。后者被解释为反映G蛋白的GDP和GTP复合形式之间的平衡状态。用优先刺激红色视杆光感受器的500nm窄带光,一系列强度范围覆盖约5个对数单位,使cGMP代谢通量增加超过10倍。然而,在强度的前2.5个对数单位上,cGMP代谢反应的特征与较高强度下的特征很容易区分,较高强度下表现出强度和时间依赖性过程的逐渐衰减。在低强度范围(0.6 - 3 log光子·微米-2·秒-1)内,代谢反应的特征为:1)cGMP水解通量增加高达8倍,作为光刺激强度的对数函数,持续至少200秒;2)总cGMP浓度略有增加或无变化;3)代谢活性GDP浓度大幅增加高达10倍,作为强度的线性函数,总GDP或GTP的组织浓度无显著变化;4)每个光异构化事件通过约10,000个cGMP分子的代谢放大光信号,主要放大位点在漂白视紫红质与G蛋白相互作用水平。(摘要截短于250字)

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