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代谢疾病的分子生物学:酶活性调节缺陷

Molecular biology of metabolic disease: defects in the regulation of enzymic activity.

作者信息

Galton D J

出版信息

Enzyme. 1978;23(4):274-88. doi: 10.1159/000458589.

Abstract

The Jacob-Monod model for the regulation of enzymic activity has been used in the analysis of some types of metabolic disease. Three lesions have been considered: (1) loss of allosteric inhibition of phosphofructokinase by citrate in the condition of lipomatosis; (2) failure of covalent modification of triglyceride lipase from inactive to active forms in the condition of triglyceride storage disease, and (3) failure of repression of HMG-CoA reductase by a mutant low-density liprotein in a new variant-of familial hypercholesterolaemia. Defects in enzymic regulation are contrasted with catalytic defects (the inborn errors); the major difference being an accumulation of a normal metabolic end-product of an unregulated pathway, rather than accumulation of an unusual intermediary metabolite as in the inborn errors.

摘要

雅各布 - 莫诺德酶活性调节模型已用于分析某些类型的代谢疾病。已考虑三种病变情况:(1)在脂肪瘤病状态下,柠檬酸对磷酸果糖激酶的变构抑制作用丧失;(2)在甘油三酯储存疾病状态下,甘油三酯脂肪酶从无活性形式到活性形式的共价修饰失败;以及(3)在家族性高胆固醇血症的一种新变体中,突变的低密度脂蛋白对HMG - CoA还原酶的阻遏失败。酶调节缺陷与催化缺陷(先天性代谢缺陷)形成对比;主要区别在于未调节途径的正常代谢终产物积累,而不是像先天性代谢缺陷那样积累异常中间代谢物。

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