Nanoff C, Freissmuth M
Institute of Pharmacology, Vienna University, Austria.
Physiol Res. 1997;46(2):79-87.
The model for studying the mechanism of G protein-mediated signalling cannot account for the observation that high-affinity binding of agonists to many different receptors is not dissociated by the addition of high concentrations of guanine nucleotides. Using the cerebral A1-adenosine receptor as a model system, we have recently identified a component which is responsible for this phenomenon. This protein, termed the coupling cofactor, can be solubilized from brain membranes and chromatographically resolved from both the G proteins and the receptor. Following reconstitution into appropriate acceptor membranes, the coupling cofactor confers resistance of high-affinity agonist binding to guanine nucleotides. The coupling cofactor acts as a brake and limits receptor-dependent signal amplification; in addition, it is a candidate for participating in the higher level organization of receptors and G proteins in membranes and in the membrane-delimited cross-talk between individual receptors. Here, we present a working hypothesis on the possible biological roles of the coupling cofactor.
用于研究G蛋白介导信号传导机制的模型无法解释以下现象:向许多不同受体中加入高浓度鸟嘌呤核苷酸后,激动剂的高亲和力结合并未解离。以脑A1 - 腺苷受体作为模型系统,我们最近鉴定出一种导致该现象的成分。这种蛋白质被称为偶联辅因子,它可以从脑膜中溶解出来,并通过色谱法与G蛋白和受体分离。在重构到合适的受体膜中后,偶联辅因子赋予高亲和力激动剂结合对鸟嘌呤核苷酸的抗性。偶联辅因子起到制动器的作用,限制受体依赖性信号放大;此外,它还是参与膜中受体和G蛋白的更高层次组织以及单个受体之间膜界定的相互作用的候选者。在此,我们提出关于偶联辅因子可能生物学作用的一个工作假说。