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转导蛋白与视紫红质的相互作用。正协同行为的证据。

Transducin interactions with rhodopsin. Evidence for positive cooperative behavior.

作者信息

Wessling-Resnick M, Johnson G L

出版信息

J Biol Chem. 1987 Sep 15;262(26):12444-7.

PMID:3114258
Abstract

Transducin and rhodopsin belong to a family of guanine nucleotide-binding (G) protein-coupled receptor systems that provide signal transduction mechanisms resulting in numerous metabolic responses in a variety of cell types. A simple, direct binding assay has been developed to investigate the molecular interactions between transducin and rhodopsin. The binding curves generated by these studies are sigmoidal, indicating an allosteric response. The Scatchard plots of this data display an asymptotic, bell-shaped character representative of the positive cooperative behavior. A Hill coefficient, nH = 1.92, was determined and found to be in close agreement with previous kinetic studies of allosterism described for rhodopsin's catalytic mechanism (Wessling-Resnick, M., and Johnson G.L. (1987) J. Biol. Chem. 262, 3697-3705). The value for Kd app was determined to be 0.05 microM. Bmax values obtained from the binding studies suggest that oligomeric complexes of rhodopsin may be involved in interactions with transducin to form multiple high affinity binding sites for the G protein. The positive cooperative behavior demonstrated in this investigation can provide insight into the molecular basis for regulation of other G protein-coupled receptor systems.

摘要

转导蛋白和视紫红质属于鸟嘌呤核苷酸结合(G)蛋白偶联受体系统家族,该系统提供信号转导机制,在多种细胞类型中引发众多代谢反应。已开发出一种简单、直接的结合测定法来研究转导蛋白和视紫红质之间的分子相互作用。这些研究产生的结合曲线呈S形,表明存在变构反应。该数据的Scatchard图显示出渐近的钟形特征,代表正协同行为。确定了希尔系数nH = 1.92,发现其与先前对视紫红质催化机制变构作用的动力学研究结果非常一致(Wessling-Resnick, M., and Johnson G.L. (1987) J. Biol. Chem. 262, 3697 - 3705)。测定的Kd app值为0.05 microM。结合研究获得的Bmax值表明,视紫红质的寡聚复合物可能参与与转导蛋白的相互作用,为G蛋白形成多个高亲和力结合位点。本研究中证明的正协同行为可为其他G蛋白偶联受体系统的调节分子基础提供见解。

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