Talako S A
Biokhimiia. 1992 Nov;57(11):1733-43.
A detailed description of the dynamic aspect of the previously proposed concept concerning the domain organization of receptor molecules in biological membranes is presented. Within the framework of this model, receptor molecules are considered as structural elements of the cyclic process of receptor domain (RD) formation and decay. It is assumed that receptor molecules may form a molecular basis of various physiological cyclic processes. Different pathways of biochemical control over RD formation and their putative functional roles in various receptor systems are discussed. It is suggested that phosphatidylinositol metabolism in the cell may be coupled to biochemical control over RD formation. Two probable pathways of such control, one chemical (ligand-mediated) and one autonomous, are proposed. The molecular origin of carcinogenesis is postulated.
本文详细描述了先前提出的关于生物膜中受体分子结构域组织的动态概念。在此模型框架内,受体分子被视为受体结构域(RD)形成和衰变循环过程的结构要素。假定受体分子可能构成各种生理循环过程的分子基础。讨论了对RD形成进行生化控制的不同途径及其在各种受体系统中的假定功能作用。提示细胞中的磷脂酰肌醇代谢可能与对RD形成的生化控制相关联。提出了这种控制的两种可能途径,一种是化学途径(配体介导),另一种是自主途径。还假定了致癌作用的分子起源。