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Cell-free production, purification and characterization of human mitochondrial ADP/ATP carriers

Authors :
Delphine Baud
Stéphanie Ravaud
Céline Juillan-Binard
Aleksandra Woznicka-Misaila
Eva Pebay-Peyroula
Institut de biologie structurale (IBS - UMR 5075 )
Université Grenoble Alpes [2016-2019] (UGA [2016-2019])-Institut de Recherche Interdisciplinaire de Grenoble (IRIG)
Direction de Recherche Fondamentale (CEA) (DRF (CEA))
Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Direction de Recherche Fondamentale (CEA) (DRF (CEA))
Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Centre National de la Recherche Scientifique (CNRS)
Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes [2016-2019] (UGA [2016-2019])-Institut de Recherche Interdisciplinaire de Grenoble (IRIG)
Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)
Source :
Protein Expression and Purification, Protein Expression and Purification, Elsevier, 2018, 144, pp.46-54. ⟨10.1016/j.pep.2017.11.008⟩, Protein Expression and Purification, 2018, 144, pp.46-54. ⟨10.1016/j.pep.2017.11.008⟩
Publication Year :
2018
Publisher :
Elsevier BV, 2018.

Abstract

International audience; Mitochondrial Carriers (MCs) are responsible for fluent traffic of a variety of compounds that need to be shuttled via mitochondrial inner membranes to maintain cell metabolism. The ADP/ATP Carriers (AACs) are responsible for the import of ADP inside the mitochondria and the export of newly synthesized ATP. In human, four different AACs isoforms are described which are expressed in tissue-specific manner. They are involved in different genetic diseases and play a role in cancerogenesis. Up to now only the structures of the bovine (isoform 1) and yeast (isoforms 2 and 3) AAC have been determined in one particular conformation, obtained in complex with the CATR inhibitor. Herein, we report that full-length human ADP/ATP Carriers isoform 1 and 3 were successfully expressed in cell-free system and purified in milligram amounts in detergent-solubilized state. The proteins exhibited the expected secondary structure content. Thermostability profiles showing stabilization by the CATR inhibitor suggest that the carriers are well folded.

Details

ISSN :
10465928 and 10960279
Volume :
144
Database :
OpenAIRE
Journal :
Protein Expression and Purification
Accession number :
edsair.doi.dedup.....3b01bc2dc3085db36313c03815d91823
Full Text :
https://doi.org/10.1016/j.pep.2017.11.008