Use of in-gel peroxidase assay for cytochrome c to visualize mitochondrial complexes III and IV

• Published in: Biology open 2020-01, Vol.9 (1)
• Main Authors: Hara, Tsukasa, Shibata, Yuma, Amagai, Ryosuke, Okado-Matsumoto, Ayako
• Format: Article
• Language: English
• Subjects: Chemiluminescence; Cytochrome; Cytochrome c; Cytochromes; Electron transport; Electrophoresis; enhanced chemiluminescence; Enzymatic activity; Gel electrophoresis; high-resolution clear native polyacrylamide gel electrophoresis; Immunoglobulin A; in-gel activity assay; Investigations; Methods & Techniques; Mitochondria; mitochondrial respiratory chain complexes; oxidative phosphorylation; Peroxidase; Polyacrylamide; Proteins; Sodium dodecyl sulfate; Sodium lauryl sulfate; Substrates; supercomplex; Ubiquinol; Western blotting
• ISSN: 2046-6390; 2046-6390
• DOI: 10.1242/bio.047936

The in-gel activity assay (IGA) is a powerful technique that uses enzymatic activity and compares intensities of detected bands in mitochondrial respiratory chain supercomplexes, and it is applicable to eukaryotic organisms. However, no IGA has been established for complex III because of the difficulty of access by ubiquinol, a substrate for complex III. Herein, we demonstrate that cytochrome (Cyt ) showed peroxidase activity on IGA as a component of complexes III and IV. We used pre-incubation with sodium dodecyl sulfate (SDS) before IGA to loosen complexes in the gel after high-resolution clear native polyacrylamide gel electrophoresis (hrCN-PAGE), a refinement of blue native PAGE. The signals of IGA based on peroxidase activity were obtained using enhanced chemiluminescence solution. Then, the gel was directly used in western blotting or hrCN/SDS two-dimensional PAGE. Our findings indicate that IGA for Cyt reflected the indirect activity of complexes III and IV.