Kay Schink
@kschink.bsky.social
1.3K followers 1K following 9 posts
Cell Biologist interested in membrane trafficking, phosphoinositides, macropinosomes and fancy microscopes. Associate Professor, UiO
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Reposted by Kay Schink
retof.bsky.social
We present multi-immersion Oblique Plane microscope (miOPM), a light-sheet platform that can be adapted to a wide range of applications, from sensitive live cell imaging to imaging organs and cleared tissues.
www.biorxiv.org/content/10.1...
Reposted by Kay Schink
nadlerlab.bsky.social
Out today in @nature.com: Together with the Honigmann, Shevchenko, Drobot and Hof labs, we present a general workflow for imaging the localization and transport of individual lipids in cells and mapping their metabolism.
www.nature.com/articles/s41...
kschink.bsky.social
Amazing story, André. Congratulations!
Reposted by Kay Schink
clausenlab.bsky.social
big one! a decade in the making. nadler & team develop tools to track lipid transport in living cells at single-species resolution. turns out non-vesicular, asymmetry-driven transport is the main architect of organelle identity. feels like the dawn of a golden era for lipid biology. rdcu.be/eBGJv
Quantitative imaging of lipid transport in mammalian cells
Nature - Directional, non-vesicular lipid transport is responsible for fast, species-selective lipid sorting into organelle membranes.
rdcu.be
Reposted by Kay Schink
tafesselab.bsky.social
Have you published lipid-protein interactome data? Please let us know, we’d love to include it in the repository. The goal is to build a centralized hub for the scientific community.

Huge thanks to Gaelen Guzman, a graduate student/postdoc in the lab who built it from scratch.
Reposted by Kay Schink
ragnhildes.bsky.social
We are hiring! A 3-year postdoc in #Chromatin #Cancer #Epigenetics at University of Oslo, Norway and co-supervised by @amathelier.bsky.social You will be part of @cancelluio.bosky.social. We focus on #Sarcoma #Epigenome #CRISPR and Drug screen studies. Find out more and apply here: shorturl.at/DtLHM
Postdoctoral Research Fellowship in Chromatin Biology and Cancer Epigenetics (283381) | University of Oslo
Job title: Postdoctoral Research Fellowship in Chromatin Biology and Cancer Epigenetics (283381), Employer: University of Oslo, Deadline: Wednesday, August 20, 2025
shorturl.at
Reposted by Kay Schink
amathelier.bsky.social
🚨 We're hiring! NCMBM @ncmbm.bsky.social is looking for 2 new group leaders to join our vibrant research community. Ready to build your own group with strong support and a solid startup package?

Interested and attending #ISMBECCB2025? Let’s connect!

🔗 www.jobbnorge.no/en/available...
Group Leader (282908) | University of Oslo
Job title: Group Leader (282908), Employer: University of Oslo, Deadline: Monday, September 8, 2025
www.jobbnorge.no
Reposted by Kay Schink
amsikking.bsky.social
The power of basic optical design knowledge and CAD!

-> Here's a fast laser point scanner that connects to a commercial microscope. The design, build and alignment are relatively simple. Much harder is agile software control that integrates with the existing system... Custom hardware is hard!
Reposted by Kay Schink
felixmendu.bsky.social
Announcing a new @embo.org Workshop on "Intracellular mechanics and organelle mechanobiology" that we are organizing with Michael Krieg and Verena Ruprecht at @icfo.eu (Barcelona) on 16-20 February, 2026. Please, repost and spread the word! 🙏 #EMBOmechanobio

meetings.embo.org/event/26-org...
Intracellular mechanics and organelle mechanobiology
Mechanobiology is an interdisciplinary field that emerges at the cross-section of biology, physics and engineering. It aims to understand how living cells, tissues and animals sense and respond to me…
meetings.embo.org
Reposted by Kay Schink
joachimgoedhart.bsky.social
De novo designed bright, hyperstable rhodamine binders for fluorescence microscopy by Bo Huang and team: www.biorxiv.org/content/10.1...
Fig. 4 Super-resolution microscopy in live and fixed cells with Rhobin.
(A) Rhobin transiently binds rhodamine molecules and thereby constantly replenishes signal lost
through photobleaching of dyes. (B-D) No-wash STED microscopy of live U2OS cells transiently
expressing LifeAct-Rhobin2 labeled with 100 nM JFX650. (C, D) Zoom-ins of regions highlighted
in (B) imaged either with confocal or STED microscopy. Scale bar: 20 μm (B) and 10 μm (C, D).
(E-H) Rhobin enables timelapse STED microscopy of fast ER dynamics with minimal signal loss.
U2OS stably expressing N-terminal tag fusions of SEC61B were stained with 1 μM Halo-JFX650
(HaloTag7, reHaloF) or 2 μM SiRhP (Rhobin2) and imaged at a frame rate of 0.387 fps for at least
100 time points. (F, G) Selected frames from timelapse acquisitions of Rhobin2:SEC61B labeled
with SiRhP (F) or HaloTag7:SEC61B labeled with Halo-JFX650 (G). Scale bar: 2 μm. (H) Signal
.CC-BY-NC 4.0 International licenseavailable under a
(which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made
The copyright holder for this preprintthis version posted June 25, 2025.;https://doi.org/10.1101/2025.06.24.661379doi:bioRxiv preprint
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loss during timelapse imaging. Mean ± SD signal inside cells over time for indicated constructs.
(I-K) PAINT-type super-resolution microscopy with Rhobin. Rhobin2-SEC61B was transiently
expressed in U2OS cells and labeled with 5 nM SiRhP after chemical fixation. Imaging under no-
wash conditions and near-TIRF illumination. (I) Repeated, but transient binding of SiRhP
molecules to Rhobin2 at low nanomolar concentrations can be observed as intensity bursts in
intensity time traces extracted from a diffraction-limited area. See movie S3 for raw data of
binding-induced blinking. (J) Sum image across 10,000 frames of an image stack, simulating a
diffraction-limited image. (K). Reconstructed image from localized molecules in the full stack.
Reposted by Kay Schink
drmichaelway.bsky.social
🔎 Looking to start a PhD in Sept 2025?
The Crick Institute spring round for PhD recruitment is open!
If you are interested in actin cytoskeleton and imaging 🔬 then check out my project on role of Arp2/3 iso-complexes in regulating invadopodia👇please RT

www.crick.ac.uk/careers-stud...
Reposted by Kay Schink
Reposted by Kay Schink
Reposted by Kay Schink
pasteur.fr
Welcome to the official Bluesky page of the Institut Pasteur!

🔬 Explore with us the frontiers of biomedical research

🧪 Follow us to uncover groundbreaking discoveries

💡 Share knowledge for global health

🌍 Join a community passionate about progress and open science.
Reposted by Kay Schink
jytinevez.bsky.social
Pasteur is on bluesky!
pasteur.fr
The Institut Pasteur has decided to leave X (formerly Twitter) to join BlueSky! 🦋
The Institut Pasteur made this decision due to several serious issues observed on the X platform since its acquisition. Join us here to continue advocating for science. www.pasteur.fr/en/home/pres...
Institut Pasteur decides to leave X
The Institut Pasteur, a research organization which for more than 130 years has been committed to tackling infectious diseases, sharing knowledge and defending science, has decided to leave X because ...
www.pasteur.fr
Reposted by Kay Schink
robertarkowitz.bsky.social
Very nice
clairedeo.bsky.social
We made a photoswitchable HaloTag (psHaloTag), which can reversibly turn-on fluorogenic dyes upon illumination 💡. Congrats to Franzi, Bego and all co-authors, check out our preprint below 👇
www.biorxiv.org/content/10.1...
Reposted by Kay Schink
christlet.bsky.social
How it started How it's going
Reposted by Kay Schink
loogerl.bsky.social
have ppl found any funders that support toolmaking? I want to keep making tools for people, but there is a seemingly irresistible force pushing us towards hypothesis-driven research. In my experience, funders don't want to hear about tech dev. Any insights? for both neuro & climate would be great tx
Reposted by Kay Schink
chrmosimann.bsky.social
"Till you have sequence confirmation, you are not cloning but clowning." 🧬⭕🤡
- Lab Saying.

#PILife #AlwaysBeCloning