@article {4058,
	title = {Phasing electron diffraction data by molecular replacement: strategy for structure determination and refinement.},
	journal = {Methods in Molecular Biology},
	volume = {955},
	year = {2013},
	month = {2013},
	pages = {243-72},
	abstract = {<p>Electron crystallography is arguably the only electron cryomicroscopy (cryo EM) technique able to deliver atomic resolution data (better then 3 {\r A}) for membrane proteins embedded in a membrane. The progress in hardware improvements and sample preparation for diffraction analysis resulted in a number of recent examples where increasingly higher resolutions were achieved. Other chapters in this book detail the improvements in hardware and delve into the intricate art of sample preparation for microscopy and electron diffraction data collection and processing. In this chapter, we describe in detail the protocols for molecular replacement for electron diffraction studies. The use of a search model for phasing electron diffraction data essentially eliminates the need of acquiring image data rendering it immune to aberrations from drift and charging effects that effectively lower the attainable resolution.</p>
},
	issn = {1940-6029},
	doi = {10.1007/978-1-62703-176-9_14},
	author = {Wisedchaisri, G and Gonen, T}
}
