Henri Niskanen
@henriniskanen.bsky.social
94 followers 100 following 18 posts
Postdoc @ Hnisz lab | Max Planck Institute for Molecule Genetics, Berlin | Condensates & Gene regulation | Past: PhD (Molecular Medicine, Uni. East Finland) MSc (biochemistry, Uni. Turku)
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Reposted by Henri Niskanen
bulutkarslioglu.bsky.social
⚠️ I am really excited to share the work of Anastasios Balaskas, an excellent PhD candidate in the lab, with the wider world. Tasos made a significant advance: generating a stem cell-based embryo model that contains both posterior and anterior neural tissues of the late-stage gastrulating embryo.
Reposted by Henri Niskanen
akispapantonis.bsky.social
This is a piece that I and @karsten-rippe.bsky.social discussing a lot, and a topic that is very close to my heart. The editors @naturerevgenet.bsky.social gave us the stage to do so, and the final version of our review is now available under this link: rdcu.be/erP1u

A short thread follows 1/n
Reposted by Henri Niskanen
molgen.mpg.de
Work is a collaboration with @matthewkraushar.bsky.social, @aktast.bsky.social and the MPIMG Service Groups FACS, microscopy, sequencing and mass spec, as well as researchers from Austria, the US and Switzerland. Link to the publication:
www.nature.com/articles/s41...
Reposted by Henri Niskanen
molgen.mpg.de
In @nature.com Yaotian Zhang and @henriniskanen.bsky.social from the Hnisz Lab discovered a micropeptide, the "Killswitch," which alters the physical state of biomolecules in condensates. This tool solidifies dynamic, liquid-like droplets, affecting their function.
--> www.molgen.mpg.de/4884827
Reposted by Henri Niskanen
sshadan.bsky.social
A bottleneck for studying the biological function of biomolecular condensates is unavailability of tools to selectively probe them within living cells. @nature, researchers report one such tool, showcasing its use in various contexts including disease. www.nature.com/articles/s41...
Probing condensate microenvironments with a micropeptide killswitch - Nature
Targeting a non-natural micropeptide ‘killswitch’ to several biomolecular condensates altered condensate compositions and revealed condensate functions in human cells
www.nature.com
henriniskanen.bsky.social
7/7
In summary, the killswitch is a versatile tool that alters condensate material properties in live cells. It revealed that condensate composition and functions rely on their microenvironments, paving the way for new biology and therapeutic strategies
henriniskanen.bsky.social
6/7
In zebrafish embryos, killswitch targeted to transcriptional condensates via NANOG suppressed miRNA transcription. Across models, killswitch reveals functional consequences of changing condensate material property, without dissolving the structures themselves.
henriniskanen.bsky.social
5/7
In adenoviral 52K condensates, killswitch reduced dynamics and blocked recruitment of capsid protein IIIa, despite preserved binding interfaces. Viral progeny production dropped >90%. The KS thus uncovers hidden roles of condensate microenvironments for condensate regulation.
henriniskanen.bsky.social
4/7
Targeting BRD4::NUT condensates with killswitch disrupted RNA Pol II partitioning and reduced transcription. In NUP98::KDM5A-driven AML cells, killswitch caused proteasome-mediated degradation of fusion condensates and impaired leukemia cell growth.
henriniskanen.bsky.social
3/7
To analyze compositional changes, we developed NuFANCI, a FACS-based method to isolate nuclear condensates. Applied to killswitch-targeted nucleoli, mass spectrometry revealed selective depletion of ~20 RNA-binding proteins, demonstrating condensate-material-property–dependent partitioning.
henriniskanen.bsky.social
2/7
Using the nanobody system, killswitch can be targeted to a wide range of endogenous condensates, including nucleoli, nuclear speckles, chromocenters, and disease-specific condensates.
henriniskanen.bsky.social
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Killswitch (KS) is a non-natural, self-associating micropeptide that can be genetically fused to condensate proteins or recruited via GFP-nanobody. It immobilizes scaffold proteins without affecting soluble pools—letting us perturb condensates selectively in live cells.
henriniskanen.bsky.social
Special thanks to the great team that made this work possible: @idamarii.bsky.social Pablo Fernandez-Pernas, Melanie A, Matt C, Alex M, Melanie P-S @nvastenhouw.bsky.social ‪@weitzmanlab.bsky.social @floriangrebien.bsky.social @aktast.bsky.social @molgen.mpg.de @childrensphila.bsky.social
henriniskanen.bsky.social
What controls condensate composition and function beyond binding stoichiometry? We show that condensate microenvironments play a key role, and can be probed by a micropeptide killswitch in live cells. www.nature.com/articles/s41... in @nature.com ‬ with @yaotianzhang.bsky.social Denes Hnisz & team.
www.nature.com
henriniskanen.bsky.social
In summary, the killswitch is a versatile tool that alters condensate material properties in live cells. It revealed that condensate composition and functions rely on their microenvironments, paving the way for new biological insights and therapeutic strategies.
henriniskanen.bsky.social
5/7
In adenoviral 52K condensates, killswitch reduced dynamics and blocked recruitment of capsid protein IIIa, despite preserved binding interfaces. Viral progeny production dropped >90%. The KS thus uncovers hidden roles of condensate microenvironments for condensate regulation.
henriniskanen.bsky.social
4/7
Targeting BRD4::NUT condensates with killswitch disrupted RNA Pol II partitioning and reduced transcription. In NUP98::KDM5A-driven AML cells, killswitch caused proteasome-mediated degradation of fusion condensates and impaired leukemia cell growth.
henriniskanen.bsky.social
3/7
To analyze compositional changes, we developed NuFANCI, a FACS-based method to isolate nuclear condensates. Applied to killswitch-targeted nucleoli, mass spectrometry revealed selective depletion of ~20 RNA-binding proteins, demonstrating condensate-material-property–dependent partitioning.
henriniskanen.bsky.social
2/7
Using the nanobody system, killswitch can be targeted to a wide range of endogenous condensates, including nucleoli, nuclear speckles, chromocenters, and disease-specific condensates.
henriniskanen.bsky.social
Killswitch (KS) is a non-natural, self-associating micropeptide that can be genetically fused to condensate proteins or recruited via GFP-nanobody. It immobilizes scaffold proteins without affecting soluble pools—letting us perturb condensates selectively in live cells.
henriniskanen.bsky.social
Special thanks to the great team that made this work possible: @idamarii.bsky.social Pablo, Melanie, Matt, Alex, Melanie P-S. @nvastenhouw.bsky.social ‪‪ @floriangrebien.bsky.social @matthewkraushar.bsky.social @aktast.bsky.social @molgen.mpg.de