Takashi Tatsuta
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Explore the profile of Takashi Tatsuta including associated specialties, affiliations and a list of published articles.
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46
Citations
2708
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Recent Articles
1.
Tiku V, Fakih Z, Tatsuta T, Jung M, Rapaport D, Dimmer K
J Biol Chem
. 2025 Jan;
301(3):108217.
PMID: 39863106
Mitochondria derive the majority of their lipids from other organelles through contact sites. These lipids, primarily phosphoglycerolipids, are the main components of mitochondrial membranes. In the cell, neutral lipids like...
2.
Sawczyc H, Tatsuta T, Oster C, Kosteletos S, Lange S, Bohg C, et al.
Nat Commun
. 2024 Aug;
15(1):7533.
PMID: 39215029
Polymers can facilitate detergent-free extraction of membrane proteins into nanodiscs (e.g., SMALPs, DIBMALPs), incorporating both integral membrane proteins as well as co-extracted native membrane lipids. Lipid-only SMALPs and DIBMALPs have...
3.
Kohler A, Carlstrom A, Nolte H, Kohler V, Jung S, Sridhara S, et al.
Mol Cell
. 2023 Sep;
83(19):3470-3484.e8.
PMID: 37751741
Folding of newly synthesized proteins poses challenges for a functional proteome. Dedicated protein quality control (PQC) systems either promote the folding of nascent polypeptides at ribosomes or, if this fails,...
4.
Tanaka T, Tatsuta T, Ikenishi K
Dev Growth Differ
. 2023 Jun;
37(1):111-122.
PMID: 37281447
In the process of monoclonal antibody (mAb) production against the 38kDa protein which is lacking in the gastrula arrested mutant embryos in Xenopus we incidentally obtained two kinds of mAb...
5.
Deshwal S, Onishi M, Tatsuta T, Bartsch T, Cors E, Ried K, et al.
Nat Cell Biol
. 2023 Jan;
25(2):246-257.
PMID: 36658222
Coenzyme Q (or ubiquinone) is a redox-active lipid that serves as universal electron carrier in the mitochondrial respiratory chain and antioxidant in the plasma membrane limiting lipid peroxidation and ferroptosis....
6.
Miliara X, Tatsuta T, Eiyama A, Langer T, Rouse S, Matthews S
Biochim Biophys Acta Proteins Proteom
. 2022 Oct;
1871(1):140867.
PMID: 36309326
The PRELID-TRIAP1 family of proteins is responsible for lipid transfer in mitochondria. Multiple structures have been resolved of apo and lipid substrate bound forms, allowing us to begin to piece...
7.
Konig T, Nolte H, Aaltonen M, Tatsuta T, Krols M, Stroh T, et al.
Nat Cell Biol
. 2021 Dec;
23(12):1271-1286.
PMID: 34873283
Mitochondrial-derived vesicles (MDVs) are implicated in diverse physiological processes-for example, mitochondrial quality control-and are linked to various neurodegenerative diseases. However, their specific cargo composition and complex molecular biogenesis are still...
8.
Cretin E, Lopes P, Vimont E, Tatsuta T, Langer T, Gazi A, et al.
EMBO Mol Med
. 2021 May;
13(6):e13579.
PMID: 34014035
Mutations in OPA1 cause autosomal dominant optic atrophy (DOA) as well as DOA+, a phenotype characterized by more severe neurological deficits. OPA1 deficiency causes mitochondrial fragmentation and also disrupts cristae,...
9.
Laborenz J, Bykov Y, Knoringer K, Raschle M, Filker S, Prescianotto-Baschong C, et al.
Mol Biol Cell
. 2021 Feb;
32(8):664-674.
PMID: 33596095
For the biogenesis of mitochondria, hundreds of proteins need to be targeted from the cytosol into the various compartments of this organelle. The intramitochondrial targeting routes these proteins take to...
10.
Eiyama A, Aaltonen M, Nolte H, Tatsuta T, Langer T
J Biol Chem
. 2021 Jan;
296:100335.
PMID: 33497623
Lipid transfer proteins of the Ups1/PRELID1 family facilitate the transport of phospholipids across the intermembrane space of mitochondria in a lipid-specific manner. Heterodimeric complexes of yeast Ups1/Mdm35 or human PRELID1/TRIAP1...