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Summary Mitochondria & Electron Transport Chain (ETC) – Full Guide to Bioenergetics & Clinical Links

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This comprehensive document explores the structure, function, and clinical relevance of mitochondria and the electron transport chain (ETC). Designed for students in medicine, biochemistry, and life sciences, it’s perfect for mastering oxidative phosphorylation, ATP synthesis, and the role of mitochondria in health and disease. Topics Covered: Mitochondrial structure & dynamics (fusion, fission, ultrastructure) ATP synthesis & the chemiosmotic theory Detailed overview of ETC complexes I–IV and CoQ/cytochrome c Proton motive force (ΔΨ and ΔpH) Mitochondrial DNA and protein import Calcium homeostasis and MAMs ROS generation and antioxidant defense Role in apoptosis and mitochondrial diseases Clinical connections: MELAS, LHON, Parkinson’s, Warburg effect

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Biochemistry
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Uploaded on
July 24, 2025
Number of pages
11
Written in
2024/2025
Type
Summary

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Mitochondria and the Electron Transport Chain (ETC):
Comprehensive Notes



I. Introduction to Mitochondria

Mitochondria are dynamic, double-membraned organelles critical
for cellular energy metabolism. Often termed the "powerhouses
of the cell," their principal role is to generate adenosine
triphosphate (ATP) through the process of oxidative
phosphorylation. However, their functions extend far beyond
mere energy production, encompassing roles in cell signaling,
apoptosis, metabolic regulation, and biosynthetic pathways.



II. Key Functions of Mitochondria

1. ATP Production via Oxidative Phosphorylation

 The primary energy-yielding process occurs across the inner
mitochondrial membrane (IMM) via the Electron Transport
Chain (ETC) and ATP synthase.

 ATP is synthesized as electrons donated by reduced
cofactors (NADH and FADH₂) pass through ETC complexes,

, driving proton pumping and the generation of the proton
motive force (PMF).

2. Mitochondrial Genome and Protein Expression

 Mitochondria possess their own circular DNA (~16.5–17 kb)
encoding 13 essential polypeptides, 22 tRNAs, and 2 rRNAs.

 These components are crucial for the assembly and function
of ETC complexes.

 Despite this autonomy, ~99% of mitochondrial proteins are
encoded by nuclear genes, translated in the cytosol, and
imported post-translationally via specialized translocases.

3. Generation and Regulation of Reactive Oxygen Species (ROS)

 As electrons leak from the ETC, particularly at Complexes I
and III, superoxide (O₂⁻) and other ROS are formed.

 At physiological levels, ROS act as signaling molecules;
however, excess ROS lead to oxidative damage,
mitochondrial dysfunction, and disease pathogenesis.

 Antioxidant systems (e.g., superoxide dismutase, glutathione
peroxidase) mitigate oxidative stress.

4. Calcium Homeostasis
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