https://3demmethods.i2pc.es/index.php?action=history&feed=atom&title=2026Subramaniam_Review2026Subramaniam Review - Revision history2026-07-09T14:03:44ZRevision history for this page on the wikiMediaWiki 1.44.2https://3demmethods.i2pc.es/index.php?title=2026Subramaniam_Review&diff=5228&oldid=prevWikiSysop: Created page with "== Citation == Subramaniam, S., Kühlbrandt, W. and Henderson, R. 2026. Cryo-EM: the revolution continues. IUCrJ. 13, 4 (2026). == Abstract == The near-universal adoption of electron cryo-microscopy (cryo-EM) by structural and cell biologists has led to exponential growth of the field, especially over the last two decades, with a doubling in the number of deposited electronmicroscopy density maps every 2.5 years. This exponential growth has changed in recent years to..."2026-07-09T06:24:53Z<p>Created page with "== Citation == Subramaniam, S., Kühlbrandt, W. and Henderson, R. 2026. Cryo-EM: the revolution continues. IUCrJ. 13, 4 (2026). == Abstract == The near-universal adoption of electron cryo-microscopy (cryo-EM) by structural and cell biologists has led to exponential growth of the field, especially over the last two decades, with a doubling in the number of deposited electronmicroscopy density maps every 2.5 years. This exponential growth has changed in recent years to..."</p>
<p><b>New page</b></p><div>== Citation ==<br />
<br />
Subramaniam, S., Kühlbrandt, W. and Henderson, R. 2026. Cryo-EM: the revolution continues. IUCrJ. 13, 4 (2026).<br />
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== Abstract ==<br />
<br />
The near-universal adoption of electron cryo-microscopy (cryo-EM) by structural<br />
and cell biologists has led to exponential growth of the field, especially over<br />
the last two decades, with a doubling in the number of deposited electronmicroscopy<br />
density maps every 2.5 years. This exponential growth has changed<br />
in recent years to become linear. Cryo-EM methods are now able to contribute<br />
to our structural understanding of biological complexity ranging from atomic<br />
resolution maps of assemblies of multiprotein complexes to in situ investigation<br />
of protein structures in the context of intact cells, snapshots of multiple<br />
conformations and insights into fundamental chemical mechanisms underlying<br />
biological function. Combined with dramatic advances in artificial intelligence,<br />
the increasing democratization and implementation of cryo-EM appears poised<br />
to drive a new revolution in digital biology.<br />
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== Keywords ==<br />
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== Links ==<br />
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https://journals.iucr.org/m/issues/2026/04/00/hi5656/index.html<br />
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== Related software ==<br />
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== Related methods ==<br />
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== Comments ==</div>WikiSysop