One thing I had forgotten to post about this whole story: the fine people running our local cryoEM facility in Uppsala made a 3D print of this ALC1-#nucleosome structure and gifted it to me during the facility's end-of-year social event in December. What a sweet attention!

Finished reading this preprint on the ALC1-#nucleosome complex? ⬆️

The methods section details what worked, but not everything that was tried: it would be way too long for the academic article format (this methods section is already quite long).

Well, if you are curious about the thought process and decision making during data analysis, rejoice! For @HRBridges has written it all up in Part 2 of the case study in the CryoSPARC Guide!

Find it here: https://guide.cryosparc.com/processing-data/tutorials-and-case-studies/case-study-processing-of-a-novel-motor-bound-nucleosome-state-empiar-10739-part-2

Discuss it on the forum here: https://discuss.cryosparc.com/t/case-study-exploratory-processing-of-a-motor-bound-nucleosome-empiar-10739-part-2/24438
Or directly here on the Fediverse.

Case Study: processing of a novel motor-bound nucleosome state (EMPIAR-10739) - part 2 | CryoSPARC Guide

Processing EMPIAR-10739 including using 3DVA to guide classification strategies, separating low population classes, and local refinement of a flexible region.

So what does this new structure look like?

ALC1 is loosely bound to the #nucleosome, in a conformation that likely doesn't allow it to slide the nucleosome along the DNA, since the two ATPase lobes are not clamping the DNA. But we finally see the macro domain, for the first time in a nucleosome-bound structure! It interacts with the N-ATPase lobe, preventing the ATPase domain from fully clamping the DNA. So this looks a lot like an intermediate state in the transition from auto-inhibited to active ALC1.

Another striking observation from this structure is a long alpha-helix just upstream of the macro domain, that lines the nucleosome's minor super-groove.

4/5

As promised, here is a summary of this new preprint on the ALC1-nucleosome complex. 🧵

https://doi.org/10.1101/2025.11.10.687450

First, a reminder of some structural features of the #nucleosome.

Histones H2A and H2B form a negatively charged cleft exposed on the surface of the histone octamer, called the "acidic patch". It is recognized by many chromatin-binding factors. If you have read on these proteins, you have most likely already read about the acidic patch too.

One feature much less commonly mentioned is the "super-groove". The DNA wraps around the histone octamer in such a way that the major and minor grooves perfectly align across the two gyres. In 2004, Dervan, Luger and colleagues synthesized short polyamides able to bind to specific sequences across the super-groove (https://doi.org/10.1073/pnas.0401743101). They hypothesized that some chromatin-binding factors may recognize the super-groove, among other nucleosomal epitopes. Until 2025, there was no direct evidence for this.

1/5

RE: https://fediscience.org/@Guillawme/111534984107819771

Something really cool happened to me this year!

@HRBridges re-processed a #cryoEM dataset from some previous work of mine and colleagues (publicly available as EMPIAR-10739; see quoted post below for a summary of this work). She significantly improved the results we had struggled to obtain at the time of the initial analysis, and wrote it up as a case study for the CryoSPARC Guide: https://guide.cryosparc.com/processing-data/tutorials-and-case-studies/case-study-end-to-end-and-exploratory-processing-of-a-motor-bound-nucleosome-empiar-10739

This is already super cool! Even cooler: she found a structure we had not found in this dataset. And it is a significant piece of result both to complete our understanding of ALC1 (the protein under study) and more broadly to understand one more way in which chromatin-binding factors can recognize the #nucleosome
We wrote an article about it, the preprint went online in November (now trying to get it peer-reviewed, but it might take some time; I can only work on this in my free time): https://doi.org/10.1101/2025.11.10.687450

I wrote some more about the back story here: https://www.gaullier.org/en/blog/2025/12/28/new-preprint-on-alc1
Long story short: this preprint would not have materialized, had we not both attended the CCP-EM Spring Symposium this year and discussed at the poster session.

I will write a summary thread about this new preprint in the near future (hopefully before the spring semester hits me; it's going to be busy...).

Chromatin fiber's genomic 'memory' governs the building blocks of life, study reveals

Northwestern Medicine scientists have discovered new details about how the human genome produces instructions for creating proteins and cells, the building blocks of life, according to a pioneering new study published in Science Advances.

Phys.org
Chromatin fiber's genomic 'memory' governs the building blocks of life, study reveals

Northwestern Medicine scientists have discovered new details about how the human genome produces instructions for creating proteins and cells, the building blocks of life, according to a pioneering new study published in Science Advances.

Phys.org
Repressed but ready to go: How bivalency holds developmental genes in a poised state for expression

As well as being essential in the precise packaging of DNA into the space of the nucleus, histone proteins are also the site of modifications, chemical additions referred to as epigenetic marks, that control whether a gene is silenced or expressed.

Phys.org
6/n In addition to the above shown examples for #MolecularMachines, here a few more #molecules we presented in #AugmentedReality at #IdeenExpo: #Tubulin-stathmin complex, #antibody, #nucleosome particle, #SARSCoV2 #polymerase.
#DIYbio #MINT #STEM #chem #AR #education #TiltFive
A #cryoem model of the RSF–NCP complex reveals distinct binding characteristics compared with the SNF2h–NCP complex and biochemical analyses indicate that RSF possesses unique chromatin-remodeling properties #ChromatinRemodeling #RSF #Nucleosome https://t.co/ZP6ZglquKq
Cryo-EM structure and functional analysis of the chromatin remodeler RSF

RSF1 changes the chromatin-remodeling mode of SNF2h. The RSF complex does not have a nucleosome-recentering capacity and a `critical distance' exists during the action of RSF in vitro; this distance is about 24 base pairs. The RSF complex loosens parts of the nucleosome DNA and undergoes conformational change on linker DNA stimulation.

Acta Crystallographica Section F