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	<title>2023Langeberg RNAScaffold - Revision history</title>
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	<updated>2026-05-24T21:10:47Z</updated>
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		<id>https://3demmethods.i2pc.es/index.php?title=2023Langeberg_RNAScaffold&amp;diff=4903&amp;oldid=prev</id>
		<title>WikiSysop: Created page with &quot;== Citation ==  C. J. Langeberg and J. S. Kieft, “A generalizable scaffold-based approach for structure determination of RNAs by cryo-EM,” Nucleic Acids Research, vol. 51, no. 20, pp. e100–e100, 2023.  == Abstract ==  Single-particle cryo-electron microscopy (cryo-EM) can reveal the structures of large and often dynamic molecules, but smaller biomolecules remain challenging targets due to their intrinsic low signal to noise ratio. Methods to resolve small proteins...&quot;</title>
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		<updated>2024-12-27T07:53:00Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;== Citation ==  C. J. Langeberg and J. S. Kieft, “A generalizable scaffold-based approach for structure determination of RNAs by cryo-EM,” Nucleic Acids Research, vol. 51, no. 20, pp. e100–e100, 2023.  == Abstract ==  Single-particle cryo-electron microscopy (cryo-EM) can reveal the structures of large and often dynamic molecules, but smaller biomolecules remain challenging targets due to their intrinsic low signal to noise ratio. Methods to resolve small proteins...&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;
C. J. Langeberg and J. S. Kieft, “A generalizable scaffold-based approach for structure determination of RNAs by cryo-EM,” Nucleic Acids Research, vol. 51, no. 20, pp. e100–e100, 2023.&lt;br /&gt;
&lt;br /&gt;
== Abstract ==&lt;br /&gt;
&lt;br /&gt;
Single-particle cryo-electron microscopy (cryo-EM) can reveal the structures of large and often&lt;br /&gt;
dynamic molecules, but smaller biomolecules remain challenging targets due to their intrinsic low signal to&lt;br /&gt;
noise ratio. Methods to resolve small proteins have been applied but development of similar approaches for&lt;br /&gt;
small structured RNA elements have lagged. Here, we present a scaffold-based approach that we used to&lt;br /&gt;
recover maps of sub-25 kDa RNA domains to 4.5 - 5.0 Å. While lacking the detail of true high-resolution&lt;br /&gt;
maps, these are suitable for model building and preliminary structure determination. We demonstrate this&lt;br /&gt;
method faithfully recovers the structure of several RNA elements of known structure, and it promises to be&lt;br /&gt;
generalized to other RNAs without disturbing their native fold. This approach may streamline the sample&lt;br /&gt;
preparation process and reduce the optimization required for data collection. This first-generation scaffold&lt;br /&gt;
approach provides a system for RNA structure determination by cryo-EM and lays the groundwork for&lt;br /&gt;
further scaffold optimization to achieve higher resolution.&lt;br /&gt;
&lt;br /&gt;
== Keywords ==&lt;br /&gt;
&lt;br /&gt;
== Links ==&lt;br /&gt;
&lt;br /&gt;
https://academic.oup.com/nar/article/51/20/e100/7288835&lt;br /&gt;
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== Related software ==&lt;br /&gt;
&lt;br /&gt;
== Related methods ==&lt;br /&gt;
&lt;br /&gt;
== Comments ==&lt;/div&gt;</summary>
		<author><name>WikiSysop</name></author>
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