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	<title>2025Levy CryoDRGNAI - Revision history</title>
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	<updated>2026-05-24T21:11:36Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://3demmethods.i2pc.es/index.php?title=2025Levy_CryoDRGNAI&amp;diff=5044&amp;oldid=prev</id>
		<title>WikiSysop: Created page with &quot;== Citation ==  Levy, A., Raghu, R., Feathers, J.R., Grzadkowski, M., Poitevin, F., Johnston, J.D., Vallese, F., Clarke, O.B., Wetzstein, G. and Zhong, E.D. 2025. CryoDRGN-AI: neural ab initio reconstruction of challenging cryo-EM and cryo-ET datasets. Nature Methods. (2025), 1–9.  == Abstract ==  Proteins and other biomolecules form dynamic macromolecular machines that are tightly orchestrated to move, bind and perform chemistry. Cryo-electron microscopy and cryo-elec...&quot;</title>
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		<updated>2025-08-25T08:12:45Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;== Citation ==  Levy, A., Raghu, R., Feathers, J.R., Grzadkowski, M., Poitevin, F., Johnston, J.D., Vallese, F., Clarke, O.B., Wetzstein, G. and Zhong, E.D. 2025. CryoDRGN-AI: neural ab initio reconstruction of challenging cryo-EM and cryo-ET datasets. Nature Methods. (2025), 1–9.  == Abstract ==  Proteins and other biomolecules form dynamic macromolecular machines that are tightly orchestrated to move, bind and perform chemistry. Cryo-electron microscopy and cryo-elec...&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;
Levy, A., Raghu, R., Feathers, J.R., Grzadkowski, M., Poitevin, F., Johnston, J.D., Vallese, F., Clarke, O.B., Wetzstein, G. and Zhong, E.D. 2025. CryoDRGN-AI: neural ab initio reconstruction of challenging cryo-EM and cryo-ET datasets. Nature Methods. (2025), 1–9.&lt;br /&gt;
&lt;br /&gt;
== Abstract ==&lt;br /&gt;
&lt;br /&gt;
Proteins and other biomolecules form dynamic macromolecular machines&lt;br /&gt;
that are tightly orchestrated to move, bind and perform chemistry.&lt;br /&gt;
Cryo-electron microscopy and cryo-electron tomography can access&lt;br /&gt;
the intrinsic heterogeneity of these complexes and are therefore key&lt;br /&gt;
tools for understanding their function. However, three-dimensional&lt;br /&gt;
reconstruction of the collected imaging data presents a challenging&lt;br /&gt;
computational problem, especially without any starting information,&lt;br /&gt;
a setting termed ab initio reconstruction. Here we introduce cryoDRGN-AI,&lt;br /&gt;
a method leveraging an expressive neural representation and combining&lt;br /&gt;
an exhaustive search strategy with gradient-based optimization to&lt;br /&gt;
process challenging heterogeneous datasets. Using cryoDRGN-AI,&lt;br /&gt;
we reveal new conformational states in large datasets, reconstruct&lt;br /&gt;
previously unresolved motions from unfiltered datasets and demonstrate&lt;br /&gt;
ab initio reconstruction of biomolecular complexes from in situ data.&lt;br /&gt;
With this expressive and scalable model for structure determination,&lt;br /&gt;
we hope to unlock the full potential of cryo-electron microscopy and&lt;br /&gt;
cryo-electron tomography as a high-throughput tool for structural biology&lt;br /&gt;
and discovery.&lt;br /&gt;
&lt;br /&gt;
== Keywords ==&lt;br /&gt;
&lt;br /&gt;
== Links ==&lt;br /&gt;
&lt;br /&gt;
https://www.nature.com/articles/s41592-025-02720-4&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>WikiSysop</name></author>
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