Han Kim

@trancekr.bsky.social

The national center for inter-university research facilities at Seoul National University. Cryo-EM / Structural Biology

Following the PLK1 datasets, the Maltose Binding protein data from the same study is now available on EMPIAR. www.ebi.ac.uk/empiar/EMPIA... Now that both datasets are accessible, it’s a great opportunity for those interested in small protein cryo-EM processing to evaluate or test their methods.

EMPIAR-13097 High-resolution cryo-EM structure of Maltose Binding Protein

EMPIAR, the Electron Microscopy Public Image Archive centered at EMBL-EBI, is a public resource for raw electron microscopy images related to EMDB, contains micrographs, particle sets and tilt-ser...

ebi.ac.uk

So it looks like only the PLK1 kinase domain–onvansertib datasets are available right now. Not sure about the MBP datasets, but if you’re interested in small-protein cryo-EM processing, it might still be worth taking a look at the currently available data. www.ebi.ac.uk/empiar/EMPIA...

EMPIAR-13098 High-resolution cryo-EM structure of human Polo-like kinase 1 in complex with onvansertib

EMPIAR, the Electron Microscopy Public Image Archive centered at EMBL-EBI, is a public resource for raw electron microscopy images related to EMDB, contains micrographs, particle sets and tilt-ser...

ebi.ac.uk

‘CryoDUCK Tokyo Days’ day 1 off to a great start. Really nice catching up with familiar faces, and finally meeting in person people I had only known online. And somehow we already got a Tokyo Skytree reference in the slides on the first day

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The early release version of our #cryoEM work on CDK11-cyclin L-SAP30BP has now been published at Nature Communications: www.nature.com/articles/s41... We got very helpful comments from the reviewers and added more structural analysis and biochemistry to support our conclusions. Please have a look!

Cryo-EM structures of the CDK11-cyclin L-SAP30BP complex reveal mechanisms of CDK11 regulation - Nature Communications

McGeoch and co-authors use cryogenic electron microscopy and biochemistry to determine the structure of the CDK11-cyclin L-SAP30BP complex and elucidate the regulation of CDK11 by SAP30BP within the t...

nature.com

Basil Greber@bjgreber.bsky.social · 4mo ago

Have a look at our latest results on #CDK regulation, just posted as a pre-print! This study was spearheaded by PhD student Amy McGeoch. Amy has determined the #cryoEM structure of the CDK11-cyclin L-SAP30B complex, an important regulator of #spliceosome activation. www.biorxiv.org/content/10.6...

Depictions of the structure of CDK11-cyclin L-SAP30BP. Four cryo-EM densities are shown at the top, two molecules models at the bottom. CDK11 is green, cyclin L is purple, and SAP30BP is yellow.

Apoferritin: 1.67 Å from the ~3,600 micrographs (~21k by collected/Krios G4, Falcon4i, SelectrisX) Collected and processed a subset in some spare time, with some help from Claude. Still, it’s not quite there yet when it comes to picking good 2D classes or dealing with issues during processing.

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1. After going back through the RELION tutorial run with Claude and correcting several issues, the reconstruction reached 2.9 Å, matching the tutorial result. The first run had given 3.22 Å, which led me to look more carefully at what had happened in the processing. So I reviewed the workflow again.

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it’s been a while. Since I have no local workstation for data processing in my new role yet, I’ve been playing with AWS. In my downtime, I asked Claude Code to follow a RELION tutorial from scratch. With a few fixes, I got a 3.22 Å result. Not bad for AI handling routine tasks! :P

initial model - class 3d -
post-processing

I think this will be my last post on this topic. I don’t want to keep talking about the authorship issue. Even though I wasn’t directly involved in the experiments/analyses for the paper, I believe this achievement wouldn’t have been possible without the discussions I led on SNS and the work

Just received this response about why I was excluded from authorship on the small protein cryo-EM paper "We have to respect the opinions of the members who actually conducted the research. What they confirmed is that the research was conducted after Dr. Kim left the company." 1/3

When I was at BaobabAiBIO, I was hesitant to publish the results because the PLK1 map was incomplete (I wrote about my concerns on Twitter). Before quitting my job, I tried to finish at least these 2 things: - getting a complete PLK1 map - uploading MBP/PLK1 data to EMPIAR

Oli Clarke@olibclarke.bsky.social · 12mo ago

This is an *excellent* review, and I hadn’t heard of PREreview before and I love the idea! On another note (as you & Gabe highlight) looking at the PLK1 map really brings home that we need mandatory reporting of some kind of anisotropy metric - that map is not buildable, & def not close to 3Å IMHO

Starting from September, I will begin working at the Core Facility for Cell and Macromolecule Imaging and the National Center for Inter-university Research Facilities at Seoul National University to manage the cryo-EM equipment and provide research support.

Update on our kinase domain side project (37 kDa with a ligand): Previous sample had severe preferred orientation issue, pausing the project. Now back at it with new 2D classification results. Still preferred orientation persists, but we're optimistic about getting a map. keep the fingers crossed.

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Oli B. Clarke (I’m mot sure he is using bluesky or not) asked about the ice thickness of our MBP dataset. So I checked the relative ice thickness plot in cryoSPARC and compared our membrane protein dataset. Here is the result.

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Sharing our IMC20 poster here. With all the feedbacks from twitter and IMC20, we will test more MBP samples internally and externally (with help from ThermoFisher). Stay tuned.

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