4.5 Article

A method for isolating highly purified and active mitochondria from insects

期刊

JOURNAL OF INSECT PHYSIOLOGY
卷 140, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jinsphys.2022.104402

关键词

Insects; Mitochondria isolation; Purity; Integrity; Activity; Storage time

资金

  1. Natural Science Foundation of China [31960286]
  2. Yunnan Fundamental Research Projects [202001AU070076, CB22052C133A]

向作者/读者索取更多资源

This study presents a method for isolating highly purified and active mitochondria from insects. The method combines differential centrifugation and discontinuous Nycodenz density gradient centrifugation and has been validated across three orders and four insect species. The study demonstrates the removal of nonmitochondrial components and the preservation of mitochondria activity/integrity. It also highlights the importance of storing the isolated mitochondria at -20 degrees C for downstream experiments.
So far, methods that yield the high purity and activity of the isolated mitochondria from insects have not been reported and determined. Here, we develop methods that combine differential centrifugation and discontinuous Nycodenz density gradient centrifugation to isolate highly purified mitochondria from the thorax muscle of insects, and the methods were widely validated across three orders (Coleoptera, Hymenoptera, and Blattaria) covering four insect species using Western blot and transmission electron microscopy (TEM) analysis. The results showed the removal of the residual contamination with nonmitochondrial components such as nucleus, sarcolemma, cytosol, and endoplasmic reticulum. Furthermore, TEM, mitochondria staining, fluorescence detection, and flow cytometry analyses were employed to assess membrane integrity and activity of the isolated mitochondria. The results showed no loss of mitochondria activity/integrity after isolation. In addition, temporal dynamics in activity of the isolated mitochondria under commonly used laboratory temperature (-20 degrees C, 4 degrees C, and 25 degrees C) were respectively detected using a fluorescence microplate reader. The results showed that it should be avoided to store the isolated mitochondria at room temperature, and the mitochondria can meet the requirements of the most downstream experiments when they were stored at -20 degrees C. Overall, the study presented a method for isolating highly purified and active mitochondria from insects. This study firstly described a high-speed discontinuous density gradient centrifugation-based method that could be widely applied for mitochondria isolation in insects. The present study also provided an example to assess purity and integrity/activity of the isolated mitochondria.

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