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		<title>WikiSysop: Created page with &quot;== Citation ==  Arnold, William R. / Asarnow, Daniel / Cheng, Yifan. Classifying liganded states in heterogeneous single-particle cryo-EM datasets. 2022. Microscopy, Vol. 71, No. Supplement_1, p. i23-i29  == Abstract ==  A powerful aspect of single-particle cryogenic electron microscopy is its ability to determine high-resolution structures from samples containing heterogeneous mixtures of the same macromolecule in different conformational or compositional states. Beyond...&quot;</title>
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		<updated>2024-09-05T06:41:14Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;== Citation ==  Arnold, William R. / Asarnow, Daniel / Cheng, Yifan. Classifying liganded states in heterogeneous single-particle cryo-EM datasets. 2022. Microscopy, Vol. 71, No. Supplement_1, p. i23-i29  == Abstract ==  A powerful aspect of single-particle cryogenic electron microscopy is its ability to determine high-resolution structures from samples containing heterogeneous mixtures of the same macromolecule in different conformational or compositional states. Beyond...&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;
Arnold, William R. / Asarnow, Daniel / Cheng, Yifan. Classifying liganded states in heterogeneous single-particle cryo-EM datasets. 2022. Microscopy, Vol. 71, No. Supplement_1, p. i23-i29&lt;br /&gt;
&lt;br /&gt;
== Abstract ==&lt;br /&gt;
&lt;br /&gt;
A powerful aspect of single-particle cryogenic electron microscopy is its ability to determine high-resolution structures from samples containing&lt;br /&gt;
heterogeneous mixtures of the same macromolecule in different conformational or compositional states. Beyond determining structures at&lt;br /&gt;
higher resolutions, one outstanding question is if macromolecules with only subtle conformation differences, such as the same protein bound&lt;br /&gt;
with different ligands in the same binding pocket, can be separated reliably, and if information concerning binding kinetics can be derived&lt;br /&gt;
from the particle distributions of different conformations obtained in classification. In this study, we address these questions by assessing the&lt;br /&gt;
classification of synthetic heterogeneous datasets of Transient Receptor Potential Vanilloid 1 generated by combining different homogeneous&lt;br /&gt;
experimental datasets. Our results indicate that classification can isolate highly homogeneous subsets of particle for calculating high-resolution&lt;br /&gt;
structures containing individual ligands, but with limitations.&lt;br /&gt;
&lt;br /&gt;
== Keywords ==&lt;br /&gt;
&lt;br /&gt;
== Links ==&lt;br /&gt;
&lt;br /&gt;
https://academic.oup.com/jmicro/article/71/Supplement_1/i23/6414663&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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