Mitochondrial proteome research: the road ahead

被引:29
作者
Baker, Zakery N. [1 ]
Forny, Patrick [1 ]
Pagliarini, David J. [1 ,2 ,3 ]
机构
[1] Washington Univ, Sch Med, Dept Cell Biol & Physiol, St Louis, MO 63130 USA
[2] Washington Univ, Sch Med, Dept Biochem & Mol Biophys, St Louis, MO 63130 USA
[3] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63130 USA
基金
瑞士国家科学基金会; 美国国家卫生研究院;
关键词
MASS-SPECTROMETRY; LYSINE ACETYLATION; HIGH-THROUGHPUT; OPA1; ISOFORMS; DISEASE GENES; CELL-DEATH; COMPLEX; PHOSPHORYLATION; DEHYDROGENASE; MUTATIONS;
D O I
10.1038/s41580-023-00650-7
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitochondria are multifaceted organelles with key roles in anabolic and catabolic metabolism, bioenergetics, cellular signalling and nutrient sensing, and programmed cell death processes. Their diverse functions are enabled by a sophisticated set of protein components encoded by the nuclear and mitochondrial genomes. The extent and complexity of the mitochondrial proteome remained unclear for decades. This began to change 20 years ago when, driven by the emergence of mass spectrometry-based proteomics, the first draft mitochondrial proteomes were established. In the ensuing decades, further technological and computational advances helped to refine these 'maps', with current estimates of the core mammalian mitochondrial proteome ranging from 1,000 to 1,500 proteins. The creation of these compendia provided a systemic view of an organelle previously studied primarily in a reductionist fashion and has accelerated both basic scientific discovery and the diagnosis and treatment of human disease. Yet numerous challenges remain in understanding mitochondrial biology and translating this knowledge into the medical context. In this Roadmap, we propose a path forward for refining the mitochondrial protein map to enhance its discovery and therapeutic potential. We discuss how emerging technologies can assist the detection of new mitochondrial proteins, reveal their patterns of expression across diverse tissues and cell types, and provide key information on proteoforms. We highlight the power of an enhanced map for systematically defining the functions of its members. Finally, we examine the utility of an expanded, functionally annotated mitochondrial proteome in a translational setting for aiding both diagnosis of mitochondrial disease and targeting of mitochondria for treatment.
引用
收藏
页码:65 / 82
页数:18
相关论文
共 190 条
[1]  
Aebersold R, 2018, NAT CHEM BIOL, V14, P206, DOI [10.1038/NCHEMBIO.2576, 10.1038/nchembio.2576]
[2]   Pathogenic Bi-allelic Mutations in NDUFAF8 Cause Leigh Syndrome with an Isolated Complex I Deficiency [J].
Alston, Charlotte L. ;
Veling, Mike T. ;
Heidler, Juliana ;
Taylor, Lucie S. ;
Alaimo, Joseph T. ;
Sung, Andrew Y. ;
He, Langping ;
Hopton, Sila ;
Broomfield, Alexander ;
Pavaine, Julija ;
Diaz, Jullianne ;
Leon, Eyby ;
Wolf, Philipp ;
McFarland, Robert ;
Prokisch, Holger ;
Wortmann, Saskia B. ;
Bonnen, Penelope E. ;
Wittig, Ilka ;
Pagliarini, David J. ;
Taylor, Robert W. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2020, 106 (01) :92-101
[3]   Bi-allelic Mutations in NDUFA6 Establish Its Role in Early-Onset Isolated Mitochondrial Complex I Deficiency [J].
Alston, Charlotte L. ;
Heidler, Juliana ;
Dibley, Marris G. ;
Kremer, Laura S. ;
Taylor, Lucie S. ;
Fratter, Carl ;
French, Courtney E. ;
Glasgow, Ruth I. C. ;
Feichtinger, Rene G. ;
Delon, Isabelle ;
Pagnamenta, Alistair T. ;
Dolling, Helen ;
Lemonde, Hugh ;
Aiton, Neil ;
Bjornstad, Alf ;
Henneke, Lisa ;
Gaertner, Jutta ;
Thiele, Holger ;
Tauchmannova, Katerina ;
Quaghebeur, Gerardine ;
Houstek, Josef ;
Sperl, Wolfgang ;
Raymond, F. Lucy ;
Prokisch, Holger ;
Mayr, Johannes A. ;
McFarland, Robert ;
Poulton, Joanna ;
Ryan, Michael T. ;
Wittig, Ilka ;
Henneke, Marco ;
Taylor, Robert W. .
AMERICAN JOURNAL OF HUMAN GENETICS, 2018, 103 (04) :592-601
[4]   The i-AAA protease YME1L and OMA1 cleave OPA1 to balance mitochondrial fusion and fission [J].
Anand, Ruchika ;
Wai, Timothy ;
Baker, Michael J. ;
Kladt, Nikolay ;
Schauss, Astrid C. ;
Rugarli, Elena ;
Langer, Thomas .
JOURNAL OF CELL BIOLOGY, 2014, 204 (06) :919-929
[5]  
Anderson KA, 2012, ESSAYS BIOCHEM, V52, P23, DOI [10.1042/BSE0520023, 10.1042/bse0520023]
[6]   Poly(ADP-ribose) polymerase-dependent energy depletion occurs through inhibition of glycolysis [J].
Andrabi, Shaida A. ;
Umanah, George K. E. ;
Chang, Calvin ;
Stevens, Daniel A. ;
Karuppagounder, Senthilkumar S. ;
Gagne, Jean-Philippe ;
Poirier, Guy G. ;
Dawson, Valina L. ;
Dawson, Ted M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2014, 111 (28) :10209-10214
[7]   A High-Density Human Mitochondrial Proximity Interaction Network [J].
Antonicka, Hana ;
Lin, Zhen-Yuan ;
Janer, Alexandre ;
Aaltonen, Mari J. ;
Weraarpachai, Woranontee ;
Gingras, Anne-Claude ;
Shoubridge, Eric A. .
CELL METABOLISM, 2020, 32 (03) :479-+
[8]   A Genome-wide CRISPR Death Screen Identifies Genes Essential for Oxidative Phosphorylation [J].
Arroyo, Jason D. ;
Jourdain, Alexis A. ;
Calvo, Sarah E. ;
Ballarano, Carmine A. ;
Doench, John G. ;
Root, David E. ;
Mootha, Vamsi K. .
Cell Metabolism, 2016, 24 (06) :875-885
[9]   Assigning mitochondrial localization of dual localized proteins using a yeast Bi-Genomic Mitochondrial-Split-GFP [J].
Bader, Gaetan ;
Enkler, Ludovic ;
Araiso, Yuhei ;
Hemmerle, Marine ;
Binko, Krystyna ;
Baranowska, Emilia ;
De Craene, Johan-Owen ;
Ruer-Laventie, Julie ;
Pieters, Jean ;
Tribouillard-Tanvier, Deborah ;
Senger, Bruno ;
di Rago, Jean-Paul ;
Friant, Sylvie ;
Kucharczyk, Roza ;
Becker, Hubert Dominique .
ELIFE, 2020, 9 :1-24
[10]   Tissue Specific Phosphorylation of Mitochondrial Proteins Isolated from Rat Liver, Heart Muscle, and Skeletal Muscle [J].
Bak, Steffen ;
Leon, Ileana R. ;
Jensen, Ole Nerregaard ;
Hojlund, Kurt .
JOURNAL OF PROTEOME RESEARCH, 2013, 12 (10) :4327-4339