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Cell-free production, purification and characterization of human mitochondrial ADP/ATP carriers
- 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.
- Subjects :
- 0301 basic medicine
Gene isoform
Gene Expression
Mitochondrion
Cell-free protein expression
Protein Structure, Secondary
03 medical and health sciences
Mitochondrial carriers
Humans
Protein secondary structure
Mitochondrial ADP-ATP Carriers
Thermostability
Cell-Free System
[SDV.BBM.BS]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Structural Biology [q-bio.BM]
Chemistry
Yeast
030104 developmental biology
Membrane
Membrane protein
Biochemistry
ADP/ATP carrier
Crystallization
Mitochondrial ADP, ATP Translocases
Biotechnology
Subjects
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