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Mitochondria are key metabolic organelles that exhibit a high level of phenotypic plasticity in skeletal muscle. The import of proteins from the cytosol is a critical pathway for organelle biogenesis, essential for the expansion of the reticulum and the maintenance of mitochondrial function. Therefore, protein import serves as a barometer of cellular health.
Mitochondria are key metabolic and regulatory organelles that determine the energy supply as well as the overall health of the cell. In skeletal muscle, mitochondria exist in a series of complex morphologies, ranging from small oval organelles to a broad, reticulum-like network. Understanding how the mitochondrial reticulum expands and develops in response to diverse stimuli such as alterations in energy demand has long been a topic of research. A key aspect of this growth, or biogenesis, is the import of precursor proteins, originally encoded by the nuclear genome, synthesized in the cytosol, and translocated into various mitochondrial sub-compartments. Mitochondria have developed a sophisticated mechanism for this import process, involving many selective inner and outer membrane channels, known as the protein import machinery (PIM). Import into the mitochondrion is dependent on viable membrane potential and the availability of organelle-derived ATP through oxidative phosphorylation. Therefore its measurement can serve as a measure of organelle health. The PIM also exhibits a high level of adaptive plasticity in skeletal muscle that is tightly coupled to the energy status of the cell. For example, exercise training has been shown to increase import capacity, while muscle disuse reduces it, coincident with changes in markers of mitochondrial content. Although protein import is a critical step in the biogenesis and expansion of mitochondria, the process is not widely studied in skeletal muscle. Thus, this paper outlines how to use isolated and fully functional mitochondria from skeletal muscle to measure protein import capacity in order to promote a greater understanding of the methods involved and an appreciation of the importance of the pathway for organelle turnover in exercise, health, and disease.
Mitochondria are organelles that exist in complex morphologies in different cell types and are recognized to possess an increasing array of functions that are critical for cellular health. As such, they can no longer be whittled down merely to energy-producing organelles. Mitochondria are key metabolic regulators, determinants of cell fate, and signaling hubs, the functions of which can serve as useful indicators of overall cellular health. In skeletal muscle cells, electron microscopy studies reveal the presence of geographically distinct subsarcolemmal (SS) and intermyofibrillar (IMF) mitochondria, which exhibit a degree of connectivity1....
All animals used in these experiments are maintained in the animal care facility at York University. The experiments are conducted in accordance with the Canadian Council on Animal Care guidelines with approval from the York University Animal Care Committee (Permit: 2017-08).
1. Functional isolation of subsarcolemmal and intermyofibrillar mitochondria from skeletal muscle
We have extensively illustrated that this protocol is a valid assay for determining the rate of import into functional and intact isolated skeletal muscle mitochondria. In comparison to untreated conditions, the import of typical precursor proteins such as malate dehydrogenase (MDH) into the matrix is sensitive to membrane potential because it can be inhibited by valinomycin, a respiratory chain uncoupler (Figure 2A). Import is also impeded when mitochondrial inner and outer.......
Mitochondria are uniquely dependent on the expression and coordination of both the nuclear and mitochondrial genomes for their synthesis and expansion within cells. However, the nuclear genome encodes the vast majority (99%) of the mitochondrial proteome, and this underscores the importance of the protein import machinery in supporting mitochondrial biogenesis. Import also serves as an important signaling event, as failure to import can promote the initiation of the unfolded protein response and/or mitophagy
The authors would like to thank Dr. G.C. Shore of McGill University, Dr. A. Strauss of the Washington School of Medicine, and Dr. M.T. Ryan of La Trobe University for the original donations of expression plasmids that were used for this research. This work was supported by funding from the Natural Sciences and Engineering Research Council of Canada (NSERC) to D. A. Hood. D. A. Hood is also the holder of a Canada Research Chair in Cell Physiology.
....Name | Company | Catalog Number | Comments |
0.2% BSA | Sigma | A2153 | |
35S-methionine | Perkin Elmer | NEG709A500UC | Purchase requires a valid radioisotope permit |
ATP | Sigma | A7699 | |
Blotting paper; Whatman 3MM CHR Paper | Thermo Fisher | 05-714-5 | |
Cassette for film | Kodak | Kodak Xomatic | |
Centrifugation Tube | Thermo Fisher | 3138-0050 | |
Chloroform | Thermo Fisher | C298-4 | |
DTT | Sigma | D9779-5G | |
EDTA | BioShop | EDT002 | |
EGTA | Sigma | E4378 | |
Gel Dryer | BioRad | Model 583 | |
Gel Drying Kit | Sigma or BioRad | Z377570-1PAK or OW-GDF-10 | Various options are commercially available through many companies, these are just as few examples. |
Glycerol | Caledon Laboratory Chemicals | 5350-1-40 | |
HEPES | Sigma | H3375 | |
High Speed Centrifuge | Beckman Coulter | Avanti J-25 Centrifuge | |
Homogenizer | IKA | T25 Digital Ultra Turrex | |
Isoamylalcohol, or 3-methylbutanol | Sigma | I9392 | |
KAc | BioShop | POA301.500 | |
KCl | Sigma | P3911 | |
M7G | New England Biolab | S1404S | Dilute with 1000ul 20mM HEPES to make 1mM stock |
MgCl | BioShop | MAG510 | |
MgSO4 | Thermo Fisher | M65-500 | |
MOPS | BioShop | MOP001 | |
NaCl | BioShop | SOD001 | |
NTP | Thermo Fisher | R0191 | |
OCT Plasmid | - | - | Donated from Dr. G. C. Shore, McGill University, Montreal, Canada; alternative available through Addgene, plasmid #71877 |
pGEM4Z/hTom40 Plasmid | - | - | Donated from Dr. M. T. Ryan, La Trobe University, Melbourne, Australia |
pGMDH Plasmid | - | - | Donated from Dr. A. Strauss, Washington University School of Medicine |
Phenol | Sigma | P4557 | |
Phenol:Chloroform:Isoamyalcohol | Sigma | P3803 | Can also be made with the ratio provided |
Phosphorus Film | Fujifilm | BAS-IP MS 2025 | |
Rabbit reticulocyte lysate | Promega | L4960 | Avoid freeze-thaw; aliquot lysate upon arrival; amino acids are provided in the kit as well |
RNAsin | Promega | N2311 | |
Rotor for High Speed Centrifuge | Beckman Coulter | JA-25.50 | |
SDS | BioShop | SDS001.500 | Caution: harmful if ingested or inhaled, wear a mask. |
Sodium acetate | Bioshop | SAA 304 | |
Sodium Carbonate | VWR | BDH9284 | |
Sodium salicylate | Millipore Sigma | 106601 | |
Sorbitol | Sigma | S6021 | |
SP6 RNA Polymerase | Promega | P1085 | |
Spectrophotometer | Thermo Fisher | Nanodrop 2000 | |
Spermidine | Sigma | S-2626 | |
Sucrose | BioShop | SUC507 | |
T7 RNA Polymerase | Promega | P2075 | |
Tabletop Centrifuge | Thermo Fisher | AccuSpin Micro 17 | |
Trichloroacetic acid | Thermo Fisher | A322-500 | |
Tris | BioShop | TRS001 | |
β-mercaptoethanol | Sigma | M6250-100ML |
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