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Mitochondrial contact sites are protein complexes that interact with mitochondrial inner and outer membrane proteins. These sites are essential for the communication between the mitochondrial membranes and, thus, between the cytosol and the mitochondrial matrix. Here, we describe a method to identify candidates qualifying for this specific class of proteins.
Mitochondria are present in virtually all eukaryotic cells and perform essential functions that go far beyond energy production, for instance, the synthesis of iron-sulfur clusters, lipids, or proteins, Ca2+ buffering, and the induction of apoptosis. Likewise, mitochondrial dysfunction results in severe human diseases such as cancer, diabetes, and neurodegeneration. In order to perform these functions, mitochondria have to communicate with the rest of the cell across their envelope, which consists of two membranes. Therefore, these two membranes have to interact constantly. Proteinaceous contact sites between the mitochondrial inner and outer membranes are essential in this respect. So far, several contact sites have been identified. In the method described here, Saccharomyces cerevisiae mitochondria are used to isolate contact sites and, thus, identify candidates that qualify for contact site proteins. We used this method to identify the mitochondrial contact site and cristae organizing system (MICOS) complex, one of the major contact site-forming complexes in the mitochondrial inner membrane, which is conserved from yeast to humans. Recently, we further improved this method to identify a novel contact site consisting of Cqd1 and the Por1-Om14 complex.
Mitochondria perform a variety of different functions in eukaryotes, with the most well-known being the production of ATP through oxidative phosphorylation. Other functions include the production of iron-sulfur clusters, lipid synthesis, and in higher eukaryotes, Ca2+ signaling, and the induction of apoptosis1,2,3,4. These functions are inseparably linked to their complex ultrastructure.
The mitochondrial ultrastructure was first described by electron microscopy5. It was shown th....
1. Buffers and stock solutions
It is relatively easy to separate mitochondrial inner and outer membranes. However, the generation and separation of contact site-containing vesicles are much more difficult. In our opinion, two steps are critical and essential: the sonication conditions and the gradient used.
Usually, linear gradients are thought to have a better resolution compared to step gradients. However, their reproducible production is tedious and requires special equipment. Therefore, we established a method to genera.......
Mitochondrial subfractionation is a complicated experiment with several highly complex steps. Therefore, we aimed to further improve and, to a certain degree, simplify our established method32. Here, the challenges were the requirement for complicated and highly specialized equipment, which are often individual constructions, and the enormous time and energy consumption. To this end, we tried to remove the pumps and individual constructions used for casting and harvesting the linear gradient and c.......
M.E.H. acknowledges the Deutsche Forschungsgemeinschaft (DFG), project number 413985647, for financial support. The authors thank Dr. Michael Kiebler, Ludwig-Maximilians University, Munich, for his generous and extensive support. We are grateful to Walter Neupert for his scientific input, helpful discussions, and ongoing inspiration. J.F. thanks the Graduate School Life Science Munich (LSM) for support.
....Name | Company | Catalog Number | Comments |
13.2 mL, Open-Top Thinwall Ultra-Clear Tube, 14 x 89mm | Beckman Instruments, Germany | 344059 | |
50 mL, Open-Top Thickwall Polycarbonate Open-Top Tube, 29 x 104mm | Beckman Instruments, Germany | 363647 | |
A-25.50 Fixed-Angle Rotor- Aluminum, 8 x 50 mL, 25,000 rpm, 75,600 x g | Beckman Instruments, Germany | 363055 | |
Abbe refractometer | Zeiss, Germany | discontinued, any pipet controller will suffice | |
accu-jet pro Pipet Controller | Brandtech, USA | BR26320 | discontinued, any pipet controller will suffice |
Beaker 1000 mL | DWK Life Science, Germany | C118.1 | |
Branson Digital Sonifier W-250 D | Branson Ultrasonics, USA | FIS15-338-125 | |
Branson Ultrasonic 3mm TAPERED MICROTIP | Branson Ultrasonics, USA | 101-148-062 | |
Branson Ultrasonics 200- and 400-Watt Sonifiers: Rosette Cooling Cell | Branson Ultrasonics, USA | 15-338-70 | |
Centrifuge Avanti JXN-26 | Beckman Instruments, Germany | B37912 | |
Centrifuge Optima XPN-100 ultra | Beckman Instruments, Germany | 8043-30-0031 | |
cOmplete Proteaseinhibtor-Cocktail | Roche, Switzerland | 11697498001 | |
D-Sorbit | Roth, Germany | 6213 | |
EDTA (Ethylendiamin-tetraacetic acid disodium salt dihydrate) | Roth, Germany | 8043 | |
Erlenmeyer flask, 100 mL | Roth, Germany | X747.1 | |
graduated pipette, Kl. B, 25:0, 0.1 | Hirschmann, Germany | 1180170 | |
graduated pipette, Kl. B, 5:0, 0.05 | Hirschmann, Germany | 1180153 | |
ice bath | neoLab, Germany | S12651 | |
Magnetic stirrer RCT basic | IKA-Werke GmbH, Germany | Z645060GB-1EA | |
MOPS (3-(N-Morpholino)propanesulphonic acid) | Gerbu, Germany | 1081 | |
MyPipetman Select P1000 | Gilson, USA | FP10006S | |
MyPipetman Select P20 | Gilson, USA | FP10003S | |
MyPipetman Select P200 | Gilson, USA | FP10005S | |
Omnifix 1 mL | Braun, Germany | 4022495251879 | |
Phenylmethylsulfonyl fluoride (PMSF) | Serva, Germany | 32395.03 | |
STERICAN cannula 21 Gx4 4/5 0.8x120 mm | Braun, Germany | 4022495052414 | |
stirring bar, 15 mm | VWR, USA | 442-0366 | |
Sucrose | Merck, Germany | S8501 | |
SW 41 Ti Swinging-Bucket Rotor | Beckman Instruments, Germany | 331362 | |
Test tubes | Eppendorf, Germany | 3810X | |
Tissue grinders, Potter-Elvehjem type, 2 mL glass vessel | VWR, USA | 432-0200 | |
Tissue grinders, Potter-Elvehjem type, 2 mL plunger with serrated tip | VWR, USA | 432-0212 | |
Trichloroacetic acid (TCA) | Sigma Aldrich, Germany | 33731 | discontinued, any TCA will suffice (CAS: 73-03-9) |
TRIS | Roth, Germany | 4855 |
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