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Joe Goldstein and Mike Brown: from cholesterol homeostasis to new paradigms in membrane biology [Review]

机译:乔·戈德斯坦和迈克·布朗:从胆固醇稳态到膜生物学的新范式[评论]

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摘要

Joe Goldstein and Mike Brown have worked for over 30 years on the molecular basis of cholesterol homeostasis. Through the systematic use of genetics, biochemistry, molecular biology and cell biology, they have identified a complex set of interacting molecules that work coordinately to regulate cholesterol import and synthesis. Not only did they identify the crucial proteins in this pathway but also determined their function. An unexpected outcome of their work has been a new understanding of the structure and function of cell membranes. From the low-density lipoprotein receptor to sterol regulatory element binding protein (SREBP) to SREBP cleavage-activating protein to Insig-1, each protein has provided a new and fundamentally novel insight into how membranes function as molecular sensors that respond to changes in the metabolic condition of the cell by moving molecules between cellular compartments.
机译:Joe Goldstein和Mike Brown在胆固醇体内平衡的分子基础上已经工作了30多年。通过系统地利用遗传学,生物化学,分子生物学和细胞生物学,他们确定了一组复杂的相互作用分子,这些分子协同工作以调节胆固醇的导入和合成。他们不仅确定了该途径中的关键蛋白,还确定了它们的功能。他们工作的意外结果是对细胞膜的结构和功能有了新的认识。从低密度脂蛋白受体到固醇调节元件结合蛋白(SREBP)再到SREBP裂解激活蛋白到Insig-1,每种蛋白都提供了一种新的,根本上新颖的见解,即膜如何作为分子传感器响应膜的变化。通过在细胞区室之间移动分子来改变细胞的代谢状况。

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