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TOPICAL COLLECTIONS

Methods to Assess Mitochondrial Biogenesis and Bioenergetics

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Guest Editors

Gavin McStay

Gavin McStay

Liverpool John Moores University, Senior Lecturer

Dr Gavin McStay is a Senior Lecturer at Liverpool John Moores University in the United Kingdom. He completed his PhD at the University of Bristol under the supervision of Professor Andrew Halestrap and his aim was to characterize the mitochondrial permeability transition pore. He carried out his post-doctoral work with Douglas Green at St Jude Children’s Research Hospital on cell death and Alexander Tzagoloff at Columbia University on cytochrome c oxidase assembly. His current research interests focus on how mitochondrial functions are regulated. 

Mário H Barros

Mário H Barros

University of Sao Paulo-Brazil, Department of Microbiology

Dr. Mário H Barros is an Associate Professor at the Department of Microbiology- University of Sao Paulo-Brazil. He graduated in Biological Sciences (1993) and holds a PhD in Genetic Sciences (2000) from the same university. He trained as a postdoc in Alexander Tzagoloff’s laboratory at Columbia University. His study focuses on proteins of unknown function that are required for mitochondria biogenesis in the yeast Saccharomyces cerevisiae.

Collection Overview

Mitochondria represents the most significant production site of ATP in eukaryotic cells, ranging from unicellular fungi to complex multicellular metazoans. Mitochondrial ATP production is a product of gene expression from both the nuclear and mitochondrial genomes in the context of a double membrane organelle. Evaluation of gene expression and function is essential to understand how mitochondrial biogenesis is controlled to ensure the provision of efficient ATP production. Mitochondria are the hub of energy metabolism. In addition to ATP synthesis, the organelle has different functions in bioenergetic processes such as redox metabolism and signaling. This has resulted in the development and use of techniques ranging from genetic, biochemical, structural, molecular, and cellular biology approaches. This Methods Collection will highlight the diversity of techniques that assess gene expression control, protein maturation, protein complex assembly and structure, redox homeostasis, along with mitochondrial function and morphology from model systems to clinical samples. 

Articles

Reconstitution of Msp1 Extraction Activity with Fully Purified Components
5:52

Reconstitution of Msp1 Extraction Activity with Fully Purified Components

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Cited by 7

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2021

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Abstracts

Measuring Dynamic Changes in Mitochondrial Membrane Potential and Trafficking in Sensory Neurites

Amy E. Rumora1,

Eva L. Feldman1,

Stephen I. Lentz*2

1Department of Neurology, University of Michigan, Ann Arbor, MI,

2Department of Internal Medicine, Division of Metabolism, Endocrinology & Diabetes, University of Michigan, Ann Arbor, MI

Stop-flow respirometry in Drosophila as a proxy for mitochondrial function.

Richard Sejour1,

Heather Liwanag2,

Roger A. Sanguino1,

Eugenia Villa-Cuesta*1

1Adelphi University,

2California Polytechnic State University

Optimized Seahorse protocols for single-plate runs of Mito Stress and Glycolysis Stress tests using mouse BMDMs and T cells

alla Ivanova*1

1Meharry Medical School, Nashville, TN

Deciphering the foundation of acquired mitochondrial dysfunction involving magnesium, selenium, iron and coenzyme Q10 deficiencies

Roy Moncayo*1,

Helga Moncayo1

1WOMED, Karl-Kapferer-Strasse 5, Innsbruck, Austria