Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10882945 | Mitochondrion | 2012 | 7 Pages |
Abstract
The visualization and quantification of mitochondria-associated proteins with high power microscopy methods is of particular interest to investigate protein architecture in this organelle. We report the usage of a custom-made STimulated Emission Depletion (STED) fluorescence nanoscope with ~Â 30Â nm lateral resolution for protein mapping of Percoll-purified viable mitochondria from murine heart. Using this approach, we were able to quantify and resolve distinct protein clusters within mitochondria; specifically, cytochrome c oxidase subunit 2 is distributed in clusters of ~Â 28Â nm; whereas the voltage dependent anion channel 1 displays three size distributions of ~Â 33, ~Â 55 and ~Â 83Â nm.
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Authors
Harpreet Singh, Rong Lu, Pedro Felipe Gardeazábal RodrÃguez, Yong Wu, Jean Chrisostome Bopassa, Enrico Stefani, Ligia Toro,