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	<id>https://3demmethods.i2pc.es/index.php?action=history&amp;feed=atom&amp;title=2025Wu_ZeroLossCCCorrected</id>
	<title>2025Wu ZeroLossCCCorrected - Revision history</title>
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	<updated>2026-05-24T19:32:04Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://3demmethods.i2pc.es/index.php?title=2025Wu_ZeroLossCCCorrected&amp;diff=5013&amp;oldid=prev</id>
		<title>WikiSysop: Created page with &quot;== Citation ==  J. Wu et al., “Chromatic aberration (Cc) corrected cryo-EM: the structure of pseudorabies virus (PRV) using both zero-loss and energy loss electrons,” Ultramicroscopy, p. 114182, 2025.  == Abstract ==  Here we have investigated the potential improvement in imaging vitrified biological specimens with the help of a chromatic aberration (Cc)-corrector. Using a newly developed chromatic aberration-corrected electron cryomicroscope (cryo-EM), the phase con...&quot;</title>
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		<updated>2025-07-01T06:40:12Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;== Citation ==  J. Wu et al., “Chromatic aberration (Cc) corrected cryo-EM: the structure of pseudorabies virus (PRV) using both zero-loss and energy loss electrons,” Ultramicroscopy, p. 114182, 2025.  == Abstract ==  Here we have investigated the potential improvement in imaging vitrified biological specimens with the help of a chromatic aberration (Cc)-corrector. Using a newly developed chromatic aberration-corrected electron cryomicroscope (cryo-EM), the phase con...&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;
J. Wu et al., “Chromatic aberration (Cc) corrected cryo-EM: the structure of pseudorabies virus (PRV) using both zero-loss and energy loss electrons,” Ultramicroscopy, p. 114182, 2025.&lt;br /&gt;
&lt;br /&gt;
== Abstract ==&lt;br /&gt;
&lt;br /&gt;
Here we have investigated the potential improvement in imaging vitrified biological specimens with the help of a&lt;br /&gt;
chromatic aberration (Cc)-corrector. Using a newly developed chromatic aberration-corrected electron cryomicroscope&lt;br /&gt;
(cryo-EM), the phase contrast micrographs comprising signals from both the zero loss and low energy&lt;br /&gt;
loss (1-100 eV) channels were used to determine the structure of a pseudorabies virus (PRV). Using an energy&lt;br /&gt;
selecting, electron energy loss spectrometer after the Cc corrector, datasets were collected separately yet&lt;br /&gt;
sequentially on the same specimen to allow quantification of the signal in each of the respective channels. Both&lt;br /&gt;
zero-loss first and low-loss first datasets were acquired. For further comparison, datasets from non-Cc-corrected&lt;br /&gt;
cryo-EM were also collected. 3D reconstructions of the virus from all 4 above datasets are presented including&lt;br /&gt;
two maps reconstructed only from electrons having lost 18-28 eV of energy whilst transiting the specimen.&lt;br /&gt;
Although the amplitude contrast of the signals in the low-loss micrographs is opposite in sign to that of typical&lt;br /&gt;
defocused images using only elastically scattered electrons, we show that the inelastic maps also contain detailed&lt;br /&gt;
structural information which can be recovered using Cc correction. This can be verified by comparing the maps&lt;br /&gt;
from each of the channels. Interestingly, the resolution of the reconstructed volume from the low-loss electrons&lt;br /&gt;
decreases with defocus independently of the purely elastic electron images taken from the same specimen, which&lt;br /&gt;
is consistent with previous theoretical predictions and experimental measurements of specimen induced decoherence&lt;br /&gt;
using room temperature test specimens. Together, these results indicate that the inelastically scattered&lt;br /&gt;
electrons do indeed contain useful phase contrast signals, particularly for thick specimens, but their recovery&lt;br /&gt;
requires imaging as close to in-focus as possible. Combing the optical correction demonstrated here, with a&lt;br /&gt;
lossless phase plate for in focus imaging, may offer the most straightforward way to achieve this in the future.&lt;br /&gt;
&lt;br /&gt;
== Keywords ==&lt;br /&gt;
&lt;br /&gt;
== Links ==&lt;br /&gt;
&lt;br /&gt;
https://www.sciencedirect.com/science/article/pii/S0304399125000804&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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