Lipids of mitochondria

SE Horvath, G Daum - Progress in lipid research, 2013 - Elsevier
A unique organelle for studying membrane biochemistry is the mitochondrion whose
functionality depends on a coordinated supply of proteins and lipids. Mitochondria are …

Metabolism and Regulation of Glycerolipids in the Yeast Saccharomyces cerevisiae

SA Henry, SD Kohlwein, GM Carman - Genetics, 2012 - academic.oup.com
Due to its genetic tractability and increasing wealth of accessible data, the yeast
Saccharomyces cerevisiae is a model system of choice for the study of the genetics …

Autoregulatory control of mitochondrial glutathione homeostasis

Y Liu, S Liu, A Tomar, FS Yen, G Unlu, N Ropek… - Science, 2023 - science.org
Mitochondria must maintain adequate amounts of metabolites for protective and biosynthetic
functions. However, how mitochondria sense the abundance of metabolites and regulate …

Metabolism and function of mitochondrial cardiolipin

M Ren, CKL Phoon, M Schlame - Progress in lipid research, 2014 - Elsevier
Since it has been recognized that mitochondria are crucial not only for energy metabolism
but also for other cellular functions, there has been a growing interest in cardiolipin, the …

Phospholipid subcellular localization and dynamics

Y Yang, M Lee, GD Fairn - Journal of Biological Chemistry, 2018 - ASBMB
Membrane biology seeks to understand how lipids and proteins within bilayers assemble
into large structures such as organelles and the plasma membranes. Historically, lipids were …

Thematic Review Series: Glycerolipids. Cardiolipin synthesis for the assembly of bacterial and mitochondrial membranes

M Schlame - Journal of lipid research, 2008 - ASBMB
In this article, the formation of prokaryotic and eukaryotic cardiolipin is reviewed in light of its
biological function. I begin with a detailed account of the structure of cardiolipin, its …

Cardiac and skeletal muscle defects in a mouse model of human Barth syndrome

D Acehan, F Vaz, RH Houtkooper, J James… - Journal of biological …, 2011 - ASBMB
Barth syndrome is an X-linked genetic disorder caused by mutations in the tafazzin (taz)
gene and characterized by dilated cardiomyopathy, exercise intolerance, chronic fatigue …

The enzymatic function of tafazzin

Y Xu, A Malhotra, M Ren, M Schlame - Journal of Biological Chemistry, 2006 - ASBMB
Tafazzin is a putative enzyme that is involved in cardiolipin metabolism, it may carry
mutations responsible for Barth syndrome. To identify the biochemical reaction catalyzed by …

Yeast mitochondria: an overview of mitochondrial biology and the potential of mitochondrial systems biology

C Malina, C Larsson, J Nielsen - FEMS yeast research, 2018 - academic.oup.com
Mitochondria are dynamic organelles of endosymbiotic origin that are essential components
of eukaryal cells. They contain their own genetic machinery, have multicopy genomes and …

DNAJC19, a mitochondrial cochaperone associated with cardiomyopathy, forms a complex with prohibitins to regulate cardiolipin remodeling

R Richter-Dennerlein, A Korwitz, M Haag, T Tatsuta… - Cell metabolism, 2014 - cell.com
Prohibitins form large protein and lipid scaffolds in the inner membrane of mitochondria that
are required for mitochondrial morphogenesis, neuronal survival, and normal lifespan. Here …