Abstract

The chemical system for the transformation of energy in eukaryotic mitochondria has engaged researchers for almost a century. This summary of four lectures on the electron transport system in mitochondria is an introduction to the mammalian electron transport chain for those unfamiliar with mitochondrial oxidative phosphorylation. It gives references chosen to reflect the history of the field and to highlight some of the recent advances in bioenergetics. The electron transport chain converts the energy that is released as electrons are passed to carriers of progressively higher redox potential into a proton gradient across the membrane that drives adenosine triphosphate (ATP) synthesis. The electron carriers include flavins, iron–sulfur centers, heme groups, and copper to divide the redox change from reduced nicotinamide adenine dinucleotide (NADH) at −320 mV to oxygen at +800 mV into steps that allow conversion and conservation of the energy released in three major complexes (Complexes I, III, and IV) by moving protons across the mitochondrial inner membrane. The three processes of proton pumping are now known after the successful determination of the structures of the large membrane protein complexes involved. Mitochondria and their proteins play roles not only in the production of ATP but also in cell survival, for which energy supply is the key.

Highlights

  • The chemiosmotic mechanism for adenosine triphosphate (ATP) synthesis is key to aerobic energy conversion in all cells, supplying the major‐ ity of the energy required for survival, repair, growth, and reproduction of the organism

  • This article focuses on the components and mechanism of the electron transport chain (ETC) that supports oxidative phosphoryla‐ tion in mammalian mitochondria, a process described in all biochemistry textbooks, and in more advanced detail in the book Bioenergetics 4 by Nicholls and Ferguson [1]

  • Electron transfer from a low redox potential donor to a higher redox potential acceptor in three complexes is coupled to proton movement from the matrix to the inter‐ membrane space (IMS) that equilibrates with the cytosol of the cell

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Summary

Introduction

The chemiosmotic mechanism for ATP synthesis is key to aerobic energy conversion in all cells, supplying the major‐ ity of the energy required for survival, repair, growth, and reproduction of the organism. There is a wide diversity of electron transport chains across the range of lifeforms, using either light or metabolic energy as the input, with oxygen and other final electron acceptors These systems convert energy from one form (chemical or light) to another (ion gradient across an impermeable membrane and subsequently back to chemical energy in the form of ATP) and allow the energy to be conserved rather than lost as heat. It is the same in chloroplasts using energy from sunlight and in mitochondria using the chemical energy from the breakdown of sugars, proteins, and fats. Illuminating the bac‐ teriorhodopsin enabled its proton pumping, and ATP was

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