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	<title>2021Tegunov M - Revision history</title>
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	<updated>2026-05-24T21:11:36Z</updated>
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	<entry>
		<id>https://3demmethods.i2pc.es/index.php?title=2021Tegunov_M&amp;diff=3928&amp;oldid=prev</id>
		<title>WikiSysop: Created page with &quot;== Citation ==  Tegunov, D.; Xue, L.; Dienemann, C.; Cramer, P. &amp;amp; Mahamid, J. Multi-particle cryo-EM refinement with M visualizes ribosome-antibiotic complex at 3.5 &amp;Aring...&quot;</title>
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		<updated>2021-04-05T08:07:11Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;== Citation ==  Tegunov, D.; Xue, L.; Dienemann, C.; Cramer, P. &amp;amp; Mahamid, J. Multi-particle cryo-EM refinement with M visualizes ribosome-antibiotic complex at 3.5 &amp;amp;Aring...&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;
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Tegunov, D.; Xue, L.; Dienemann, C.; Cramer, P. &amp;amp;amp; Mahamid, J. Multi-particle cryo-EM refinement with M visualizes ribosome-antibiotic complex at 3.5 &amp;amp;Aring; in cells. Nature Methods, 2021, 18, 186-193 &lt;br /&gt;
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== Abstract ==&lt;br /&gt;
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Cryo-electron microscopy (cryo-EM) enables macromolecular structure determination in vitro and inside cells. In addition to aligning individual particles, accurate registration of sample motion and three-dimensional deformation during exposures are crucial for achieving high-resolution reconstructions. Here we describe M, a software tool that establishes a reference-based, multi-particle refinement framework for cryo-EM data and couples a comprehensive spatial deformation model to in silico correction of electron-optical aberrations. M provides a unified optimization framework for both frame-series and tomographic tilt-series data. We show that tilt-series data can provide the same resolution as frame-series data on a purified protein specimen, indicating that the alignment step no longer limits the resolution obtainable from tomographic data. In combination with Warp and RELION, M resolves to residue level a 70S ribosome bound to an antibiotic inside intact bacterial cells. Our work provides a computational tool that facilitates structural biology in cells. &lt;br /&gt;
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== Keywords ==&lt;br /&gt;
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== Links ==&lt;br /&gt;
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https://www.nature.com/articles/s41592-020-01054-7&lt;br /&gt;
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== Related software ==&lt;br /&gt;
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== Related methods ==&lt;br /&gt;
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== Comments ==&lt;/div&gt;</summary>
		<author><name>WikiSysop</name></author>
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