Garland P B
Institute of Cancer Research, Chester Beatty Laboratories, London.
Biosci Rep. 1991 Dec;11(6):445-74; discussion 474-5. doi: 10.1007/BF01130215.
The concept of chemiosmotic systems arises from the pioneering work of Peter Mitchell on two fronts. One is concerned with the mechanisms by which molecules are transported across membranes which are generally barriers to such transport. These mechanisms are inevitably molecular, and are now yielding their secrets to a combination of structural protein chemistry and molecular biology. The other front is more physiological, and explores the functional relationships between metabolism and transport. Nevertheless, the two fronts form a continuum of mutually related structure and function. Chemiosmotic systems provide a hierarchy of complexity, starting from say a uniporter reconstituted in a chemically defined bilayer, and proceeding to greater complexity in mitochondria, chloroplasts, eukaryotic and prokaryotic cell membranes, and multicellular systems. Their relationship to medicine is profound, because they provide many opportunities for therapeutic intervention. In this paper I present an overview of chemiosmotic systems at different levels of complexity, both molecular and biological, of their involvements in pathology, and of possible pharmacological treatment or prevention of disease.
化学渗透系统的概念源于彼得·米切尔在两个方面的开创性工作。一方面涉及分子跨膜运输的机制,而膜通常是这种运输的障碍。这些机制必然是分子层面的,现在正通过结构蛋白质化学和分子生物学的结合揭示其奥秘。另一方面更具生理学性质,探索代谢与运输之间的功能关系。然而,这两个方面构成了相互关联的结构和功能的连续统一体。化学渗透系统呈现出一个复杂性层次结构,从比如在化学定义的双层中重组的单向转运体开始,进而在线粒体、叶绿体、真核和原核细胞膜以及多细胞系统中发展出更高的复杂性。它们与医学的关系十分深远,因为它们提供了许多治疗干预的机会。在本文中,我将概述化学渗透系统在不同复杂程度(分子层面和生物学层面)上的情况,它们在病理学中的参与情况,以及疾病可能的药物治疗或预防方法。