Hynie S
Cas Lek Cesk. 1989 Feb 17;128(8):225-31.
The article summarizes new findings concerning membranous receptor-effector complexes that are stimulated by various extracellular signals like hormones, neurotransmitters, growth factors, etc. Central role in this transmembranous signalling process play so-called G regulatory proteins (they bind GTP), that ensure the activation-deactivation processes between receptor and effector (enzymes or ion channels). The examples of intracellular signals ("second messengers") are cyclic AMP, inositol-trisphosphate, diacylglycerol or the accumulated ions (e. g. Ca2+). G regulatory proteins are composed of three subunits: receptor activation leads to their dissociation and the released alpha subunit with bound GTP activates the appropriate effector. Its inactivation occurs after GTP degradation by the intrinsic GTPase activity of alpha subunit which then associates with beta gamma subunits. New findings concerning the regulatory role of G proteins enable the explanation of mutual relations between various membranous receptor-effector complexes and further they also serve as basis for the explanation of some clinical disorders that are called "receptor diseases".
本文总结了有关膜受体 - 效应器复合物的新发现,这些复合物受到各种细胞外信号(如激素、神经递质、生长因子等)的刺激。在这种跨膜信号传导过程中起核心作用的是所谓的G调节蛋白(它们结合GTP),其确保受体与效应器(酶或离子通道)之间的激活 - 失活过程。细胞内信号(“第二信使”)的例子有环磷酸腺苷、肌醇三磷酸、二酰基甘油或积累的离子(如Ca2+)。G调节蛋白由三个亚基组成:受体激活导致它们解离,释放出的结合有GTP的α亚基激活相应的效应器。α亚基的内在GTP酶活性使GTP降解后,其失活,然后α亚基与βγ亚基结合。关于G蛋白调节作用的新发现有助于解释各种膜受体 - 效应器复合物之间的相互关系,并且它们还为解释一些被称为“受体疾病”的临床病症提供了基础。