Konrad Chudzik
@konrad-chudzik.bsky.social
190 followers 310 following 16 posts
PhD Candidate in Regulatory Genome program (IRTG2403) | Robson lab - Berlin Institute for Medical Systems Biology (MDC-BIMSB) & Mundlos Lab - Max Planck Institute for Molecular Genetics | Genome Regulation, Nuclear Envelope, LADs
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Reposted by Konrad Chudzik
annaamonaco.bsky.social
Pretty surreal to see my artwork on the cover of Nature Genetics! Big congrats to @julianeg.bsky.social, @stemundi.bsky.social and the others, and thank you Juliane for letting me help bring your research to life visually.

www.nature.com/ng/volumes/5...
The cover of Nature Genetics July 2025 issue. Digital art of a mouse paw skeletal prep on dark background, digits I to IV disintegrating into viral particles. A caption says “An endogenous retrovirus causes limb malformation”.
Reposted by Konrad Chudzik
drmrobson.bsky.social
Calling all aspiring Postdocs! One extra week to apply to join our exciting HFSP-funded project to uncover how chromatin moves to function.

Deadline July 15th.

www.mdc-berlin.de/career/jobs/...
Reposted by Konrad Chudzik
evgenykvon.bsky.social
How do non-coding variants in enhancers lead to disease? Happy to share our recent work, led by @ewholling.bsky.social, in which we discovered that poised chromatin sensitizes enhancers to aberrant activation by non-coding mutations, contributing to disease. www.biorxiv.org/content/10.1... 1/
Reposted by Konrad Chudzik
Reposted by Konrad Chudzik
drmrobson.bsky.social
We're thrilled to continue our deep dive into how chromatin mechanics govern how our genomes function with our A-team @andersshansen.bsky.social @Davide Michieletto, and @Sandra Tenreiro.

A huge thanks to the @dfg.de and @hfspo.bsky.social for supporting us.

Stay tuned! PhDs/Postdocs coming soon!
mdc-berlin.bsky.social
@drmrobson.bsky.social has won two grants from @dfg.de & @hfspo.bsky.social totaling over €2 million. He and his lab now work to decode the mechanics of #chromatin, hoping to finally define its physical state and better understand how it governs gene regulation
www.mdc-berlin.de/news/news/mi...
portrait of a man
Reposted by Konrad Chudzik
mdc-berlin.bsky.social
@drmrobson.bsky.social has won two grants from @dfg.de & @hfspo.bsky.social totaling over €2 million. He and his lab now work to decode the mechanics of #chromatin, hoping to finally define its physical state and better understand how it governs gene regulation
www.mdc-berlin.de/news/news/mi...
portrait of a man
konrad-chudzik.bsky.social
Thanks also to the @stemundi.bsky.social lab where this work started and the Robson lab where it was finished! Last, my amazing supervisor @drmrobson.bsky.social who devised the inducible DamID mouse and spearheaded the project!
konrad-chudzik.bsky.social
Huge thanks to the Wunder-Kinder @imguerreiro.bsky.social, Samy & @jopkind.bsky.social without whom this project wouldn’t have happened, and to Alex and Andrea from @marionicodemi.bsky.social lab for modeling.
konrad-chudzik.bsky.social
3️⃣ So what links this pre-activation repositioning to multipotency? We find it's closely tied to increased chromatin accessibility at sites bound by key limb transcription factors. This includes several factors shown to act together via a “coordinator motif” doi.org/10.1016/j.ce...
konrad-chudzik.bsky.social
2️⃣ But not only genes reposition. Genes escape the periphery together with the surrounding enhancers and TADs that control their expression. Using polymer modeling & mutants, we show that CTCF boundaries and 3D chromatin topology prevent this repositioning from spreading to neighboring regions.
konrad-chudzik.bsky.social
1️⃣ At the start of limb formation, hundreds of genes move away from the repressive nuclear periphery in multipotent progenitors. Amazingly, this repositioning can precede gene activation by up to four developmental days (E9.5 -> E13.5), suggesting it is a key priming step for multipotency!
konrad-chudzik.bsky.social
Developmental genes have really precise expression in time and space and so must spend most of their time inactive. So how and when do they "wake up" to perform their function? Leveraging scDam&T-seq in embryonic limb development, we uncover three exciting new insights:
konrad-chudzik.bsky.social
🚨 Preprint 🚨
Ever wondered how cells prepare their genomes to enable new cell-fates? In this team up with the Kind lab, we show that genes are repositioned in the nucleus to get ready for future activation and tissue formation. Read 🧵👇 to find out how and when this happens!

doi.org/10.1101/2025...
Reconfiguration of genome-lamina interactions marks the commissioning of limb cell-fates
Diverse forms of heterochromatin block inappropriate transcription and safeguard differentiation and cell identity. Yet, how and when heterochromatin is reconfigured to facilitate changes in cell-fate...
www.biorxiv.org
Reposted by Konrad Chudzik
michaeltmont.bsky.social
I am elated to share that our manuscript describing Variant-EFFECTS, a high-throughput technology we developed to precisely and quantitatively measure the effects of CRISPR-mediated edits on gene expression, is now published at @cellpress.bsky.social: authors.elsevier.com/c/1kxgiL7PXu...
authors.elsevier.com
konrad-chudzik.bsky.social
Grateful to my wonderful collaborators worldwide:
Yuko Sato, Xingchi Yan, Simon Ulrich, @watanyatra.bsky.social, Lothar Schermelleh, Hiroshi Kimura, IrinaSolovei & my supervisor @drmrobson.bsky.social. Thank you for your hard work & support throughout! 🌍🙏
konrad-chudzik.bsky.social
Is your rim staining real, or Ab-trapping? Solutions:
✅ Increase incubation time
✅ Tissue sections (antigen retrieval)
✅ Use lower-affinity antibodies/nanobodies
✅ Check cell-to-cell expression: rims only in high-expression cells = likely artifact
konrad-chudzik.bsky.social
This artifact can impact any assay that relies on antibody diffusion, such as classic fluorescence microscopy, but also new-generation genomics techniques, such as CUT&Tag and CUT&RUN - SO WATCH OUT. See falsely peripheral H3K9Me2 Cut&Tag in mouse rod cells 👇
konrad-chudzik.bsky.social
Ab-trapping occurs when antibodies fail to penetrate due to:
1️⃣ High epitope abundance
2️⃣ High antibody affinity
3️⃣ Low diffusion rate
Any one factor is enough! Potentially affects many antibody–epitope pairs under the right conditions. Examples 👇
konrad-chudzik.bsky.social
🚨 Preprint alert 🚨
Excited to share our work on "Ab-trapping," an antibody artifact causing misleading peripheral ("rim") staining in imaging & genomics (IF, CUT&Tag, CUT&RUN). Antibodies fail to penetrate structures, accumulating at the periphery. A 🧵👇
doi.org/10.1101/2025...
Ab-trapping - a peripheral staining artifact in antibody-based microscopy and genomics
Antibodies (Ab) are essential for detecting specific epitopes in microscopy and genomics, but can produce artifacts leading to erroneous interpretations. Here, we characterize a novel artifact, Ab-tra...
doi.org
konrad-chudzik.bsky.social
Grateful to my wonderful collaborators worldwide:
Y. Sato, X. Yan, S. Urlich, @watanyatra.bsky.social, L. Schermelleh, @gfudenberg.bsky.social, H. Kimura, I. Solovei & my supervisor @mikerobson.bsky.social. Thanks for your hard work & support! 🤝🌍