@article {67669,
	title = {Development and Applications of Fluorescent Proteins for Correlative Light and Electron Microscopy},
	journal = {Microscopy and Microanalysis},
	volume = {24},
	year = {2018},
	month = {01/2018},
	pages = {2318 - 2319},
	abstract = {<p>Recent advances in super-resolution microscopy have pushed the resolution limit of light microscopy closer to that of electron microscopy. However, as they invariably rely on fluorescence, light microscopy techniques only visualize whatever gets labeled. On the other hand, while electron microscopy reveals cellular structures at the highest resolution, it offers no specificity. The information gap between the two imaging modalities can only be bridged by correlative light and electron microscopy (CLEM). Previously we have developed a probe (mEos4) whose fluorescence and photoconversion survive 0.5-1\% OsO4 fixation, allowing super-resolution visualization of organelles and fused proteins in the context of resinembedded ultrastructure in both transmission EM (TEM) and scanning EM (SEM) [1,2].</p>
},
	issn = {1431-9276},
	doi = {10.1017/S1431927618012072},
	url = {https://www.cambridge.org/core/product/identifier/S1431927618012072/type/journal_article},
	author = {Paez-Segala, Maria G. and Wang, Yalin and Iyer, Nirmala and Li, Wei-Ping and Rivlin, Patricia K. and Looger, Loren L.}
}
