@article {1160,
	title = {Approaches toward super-resolution fluorescence imaging of mitochondrial proteins using PALM.},
	journal = {Methods},
	volume = {51},
	year = {2010},
	month = {2010 Aug},
	pages = {458-63},
	abstract = {<p>Mitochondria are difficult targets for microscopy because of their small size and highly compartmentalized, membranous interior. Super-resolution fluorescence microscopy methods have recently been developed that exceed the historical limits of optical imaging. Here we outline considerations and techniques in preparing to image the relative location of mitochondrial proteins using photoactivated localization microscopy (PALM). PALM and similar methods have the capacity to dramatically increase our ability to image proteins within mitochondria, and to expand our knowledge of the location of macromolecules beyond the current limits of immunoEM.</p>
},
	keywords = {Animals, Cryoultramicrotomy, Fluorescence, Freeze Substitution, Genetic, Luminescent Proteins, Mice, Microscopy, Mitochondria, Mitochondrial Proteins, NIH 3T3 Cells, Plastic Embedding, Promoter Regions, Recombinant Fusion Proteins, Transfection},
	issn = {1095-9130},
	doi = {10.1016/j.ymeth.2010.01.001},
	author = {Brown, Timothy A and Fetter, Richard D and Tkachuk, Ariana N and Clayton, David A}
}
