Eva-Maria Schentarra
@evaschentarra.bsky.social
56 followers 77 following 12 posts
Biotechnologist - PhD student @jungmannlab.bsky.social Enjoying the little things in life using #DNAPAINT 🔬🧬 @mpibiochem.bsky.social @lmumuenchen.bsky.social @imprs-ml.bsky.social
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evaschentarra.bsky.social
Mirror, mirror on the wall... 🪞 I'm super proud to have contributed to our latest work on left-handed DNA-PAINT! Here we introduce 6 new sequences using the left-handed enantiomers of our speed-optimized DNA-PAINT palette, enabling out-of-the-box 12-plex imaging without extra hybridization steps. 🌈🔬
jungmannlab.bsky.social
Highly efficient 12-color multiplexing with speed-optimized DNA-PAINT. We are excited to share our latest paper in @natcomms.nature.com, using left-handed DNA to extend speed-optimized DNA-PAINT to 12 targets in a simple and straightforward way! 🧬👈🚀https://www.nature.com/articles/s41467-025-64228-x
Reposted by Eva-Maria Schentarra
christlet.bsky.social
Our new preprint is up! This is the main postdoc work of @wiesner-t.bsky.social focusing on exocytosis along the axon shaft and its regulation by the sub membrane actin-spectrin scaffold: www.biorxiv.org/content/10.1...
Read the thread below for a summary of our findings 🧵1/11
Reposted by Eva-Maria Schentarra
florianschueder.bsky.social
🚨 2 × PhD positions @EPFL! 🚨
Help us push the boundaries of fluorescence microscopy - DNA nanotech, custom optics & spatial omics in Lausanne 🇨🇭. Start Jan 2026. Send CV + motivation + 2 refs → [email protected]
#PhD #Hiring #microscopy #SuperResolution #SpatialOmics #DNAPAINT #FLASHPAINT
Reposted by Eva-Maria Schentarra
mpibiochem.bsky.social
Congratulations to Ralf on your election as a new EMBO member:

❕Original press release from @embo.org : www.embo.org/press-releas...
Reposted by Eva-Maria Schentarra
jungmannlab.bsky.social
Great science, great company and stunning views at our Lab retreat on Schloss Ringberg 🏰🧬🔬. Big thanks to our guests Sabrina Simoncelli, Sebastian Kobold, Thomas Schlichthärle, @massivephotonics.bsky.social & students from the @lfmilles.bsky.social and @mlsb-borgwardt.bsky.social Labs for joining!
Reposted by Eva-Maria Schentarra
lumasullo.bsky.social
Very excited to present our latest work: SPINNA, an analysis framework and software package for single-protein resolution data! 🖥️🤩

We can directly quantify stoichiometry and oligomerization from super-res (DNA-PAINT, RESI) images!! 🧬🎨
Reposted by Eva-Maria Schentarra
moniquehonsa.bsky.social
IMAGING LIGAND-RECEPTOR INTERACTIONS AT SINGLE-PROTEIN RESOLUTION WITH DNA-PAINT🔬
Ever wonder how cells "talk"? It starts when ligands bind to receptors on cell surfaces. We have cracked the challenge of imaging small ligands on cell surfaces. #DNAPAINT #celltalk 💬
doi.org/10.1002/smtd...
evaschentarra.bsky.social
Thanks to @eduardunterauer.bsky.social, @jekristina.bsky.social, @forna.bsky.social, @opazo.bsky.social and @carstenmarr.bsky.social for putting together this great step-by-step guide on how to achieve up to 30-color DNA-PAINT spatial proteomics at sub-15 nm resolution. 🚀
Reposted by Eva-Maria Schentarra
lumasullo.bsky.social
ÅNGSTRÖM-RESOLUTION IMAGING OF CELL-SURFACE GLYCANS 🧬🎨🍬

The glycocalyx, our cells' sugar coat, holds secrets in immunology, cancer, viral infections, and more. Visualizing its molecular architecture was impossible… until now. #glycotime #microscopy

www.biorxiv.org/content/10.1...
evaschentarra.bsky.social
Whipped up a DNA-themed cake for the
@JungmannLab - sweet science at its finest! 🍰🔬 #PhDlife
evaschentarra.bsky.social
Do you know what I love most about my PhD @JungmannLab? Actually seeing the things I learned from biology textbooks come to life🪄. Check out this DNA-PAINT image of the Golgi, showing both cis (GM130) and trans (TGN38) faces together with peroxisomes. Happy
#FluorescenceFriday😊
evaschentarra.bsky.social
If you're curious about imaging more than 6 targets using DNA-PAINT, take a look at our recent publication on SUM-PAINT for high-throughput multiplexing

cell.com/cell/fulltext/…
evaschentarra.bsky.social
Looking at this beautifully detailed neuron, stained for 9 different proteins using SUM-PAINT, feels like stepping into one of David S. Goodsell's paintings illustrating the crowded cellular environment. #FluorescenceFriday #phdlife @JungmannLab
evaschentarra.bsky.social
Excited to attend my first ever conference on single molecule approaches to biology by @GordonConf in beautiful Maine!
Caught a fun 'Where's Waldo' moment in the hotel lobby - can you spot Ralf Jungmann and Luciano Masullo waving at me in the background? 🔍 @JungmannLab @l_masu
evaschentarra.bsky.social
Happy Friday! To wrap up another exciting week of learning highly multiplexed DNA-PAINT in the @JungmannLab, here's a nice #cellfie of a rat hippocampal neuron stained for synaptic vesicle markers (Vamp2, VGlut1 and synaptotagmin), clathrin, neurofilament and peroxisomes.
evaschentarra.bsky.social
With this my MINFLUX chapter may has concluded for now, but this was just the kick-off to my journey into super-resolution microscopy as a PhD student @JungmannLab 🚀
evaschentarra.bsky.social
My first preprint as a joint first author together with Otto Wirth and I couldn't be more excited! 📚 🔬
Exploring kinesin with MINFLUX during my Master's thesis was a blast while working with such talented minds in the Hell Lab.

x.com/Stefan_W_Hell/… biorxiv.org/content/10.110…
Uncovering kinesin dynamics in neurites with MINFLUX
Neurons grow neurites of several tens of micrometers in length, necessitating active transport from the cell body by motor proteins. By tracking fluorophores as minimally invasive labels, MINFLUX is able to quantify the motion of those proteins with nanometer/millisecond resolution. Here we study the substeps of a truncated kinesin-1 mutant in primary rat hippocampal neurons, which have so far been mainly observed on microtubules polymerized on glass coverslips. A gentle fixation protocol largely maintains the structure and surface modifications of the microtubules in the cell. By analyzing the time between the substeps, we identify the ATP-binding state of kinesin-1 and observe the associated rotation of the kinesin-1 head in neurites. We also observed kinesin-1 switching microtubules mid-walk, highlighting the potential of MINFLUX to study the details of active cellular transport. ### Competing Interest Statement S.W.H. is inventor on patent applications WO 2013/072273 and WO 2015/097000 filed by the Max Planck Society that cover basic principles and arrangements of MINFLUX, including single-molecule tracking. S.W.H. is inventor on patent application WO 2020/064108 submitted by the Max Planck Society that covers principles and arrangements of the phase/amplitude modulator for shifting the intensity minimum. S.W.H. is a cofounder of the company Abberior Instruments, which commercializes MINFLUX microscopes. The remaining authors declare no competing interests.
www.biorxiv.org