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	<id>https://3demmethods.i2pc.es/index.php?action=history&amp;feed=atom&amp;title=2016Passmore_Review</id>
	<title>2016Passmore Review - Revision history</title>
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	<updated>2026-05-24T21:05:56Z</updated>
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	<entry>
		<id>https://3demmethods.i2pc.es/index.php?title=2016Passmore_Review&amp;diff=2891&amp;oldid=prev</id>
		<title>CoSS: Created page with &quot;== Citation ==  Passmore, L. &amp; Russo, C. J. Methods in Enzymology. The Resolution Revolution: Recent Advances In cryoEM Specimen preparation for high-resolution cryo-EM Academ...&quot;</title>
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		<updated>2016-08-31T05:03:26Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;== Citation ==  Passmore, L. &amp;amp; Russo, C. J. Methods in Enzymology. The Resolution Revolution: Recent Advances In cryoEM Specimen preparation for high-resolution cryo-EM Academ...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;== Citation ==&lt;br /&gt;
&lt;br /&gt;
Passmore, L. &amp;amp; Russo, C. J. Methods in Enzymology. The Resolution Revolution: Recent Advances In cryoEM Specimen preparation for high-resolution cryo-EM Academic Press, 2016, 51-86&lt;br /&gt;
&lt;br /&gt;
== Abstract ==&lt;br /&gt;
&lt;br /&gt;
Imaging a material with electrons at near-atomic resolution requires a thin specimen&lt;br /&gt;
that is stable in the vacuum of the transmission electron microscope. For biological samples,&lt;br /&gt;
this comprises a thin layer of frozen aqueous solution containing the biomolecular&lt;br /&gt;
complex of interest. The process of preparing a high-quality specimen is often the limiting&lt;br /&gt;
step in the determination of structures by single-particle electron cryomicroscopy&lt;br /&gt;
(cryo-EM). Here, we describe a systematic approach for going from a purified biomolecular&lt;br /&gt;
complex in aqueous solution to high-resolution electron micrographs that are suitable&lt;br /&gt;
for 3D structure determination. This includes a series of protocols for the&lt;br /&gt;
preparation of vitrified specimens on various supports, including all-gold and graphene.&lt;br /&gt;
We also describe techniques for troubleshooting when a preparation fails to yield suitable&lt;br /&gt;
specimens, and common mistakes to avoid during each part of the process. Finally,&lt;br /&gt;
we include recommendations for obtaining the highest quality micrographs from prepared&lt;br /&gt;
specimens with current microscope, detector, and support technology.&lt;br /&gt;
&lt;br /&gt;
== Keywords ==&lt;br /&gt;
&lt;br /&gt;
== Links ==&lt;br /&gt;
&lt;br /&gt;
http://www.sciencedirect.com/science/article/pii/S0076687916300295&lt;br /&gt;
&lt;br /&gt;
== Related software ==&lt;br /&gt;
&lt;br /&gt;
== Related methods ==&lt;br /&gt;
&lt;br /&gt;
== Comments ==&lt;/div&gt;</summary>
		<author><name>CoSS</name></author>
	</entry>
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