| Autor: |
Vadovsky AC; Department of Physiology, Michigan State University., Quinn M; Department of Kinesiology, Michigan State University., Xia T; Department of Physiology, Michigan State University., Levitsky Y; Department of Physiology, Michigan State University., Bazil JN; Department of Physiology, Michigan State University; jnbazil@msu.edu. |
| Jazyk: |
angličtina |
| Zdroj: |
Journal of visualized experiments : JoVE [J Vis Exp] 2024 Aug 23 (210). Date of Electronic Publication: 2024 Aug 23. |
| DOI: |
10.3791/67093 |
| Abstrakt: |
Mitochondrial isolation has been practiced for decades, following procedures established by pioneers in the fields of molecular biology and biochemistry to study metabolic impairments and disease. Consistent mitochondrial quality is necessary to properly investigate mitochondrial physiology and bioenergetics; however, many different published isolation methods are available for researchers. Although different experimental strategies require different isolation methods, the basic principles and procedures are similar. This protocol details a method capable of extracting well-coupled mitochondria from a variety of tissue sources, including small animals and cells. The steps outlined include organ dissection, mitochondrial purification, protein quantification, and various quality control checks. The primary quality control metric used to identify high-quality mitochondria is the respiratory control ratio (RCR). The RCR is the ratio of the respiratory rate during oxidative phosphorylation to the rate in the absence of ADP. Alternative metrics are discussed. While high RCR values relative to their tissue source are obtained using this protocol, several steps can be optimized to suit the individual needs of researchers. This procedure is robust and has consistently resulted in isolated mitochondria with above-average RCR values across animal models and tissue sources. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
|
