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niels-fischer.bsky.social

@niels-fischer.bsky.social
88 followers 71 following 5 posts

Group Leader @ MPI-NAT | Translation regulation in health & disease | Structural biology

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erzbergerlab.bsky.social @erzbergerlab.bsky.social · 22/07/2026
www.biorxiv.org/content/10.6...
biorxiv.org
Ribosome biogenesis bottlenecks reveal vulnerabilities in cancer
Cell growth requires elevated protein synthesis, which depends on the production of ribosomes. Ribosome biogenesis is a complex, multi-step pathway in which newly transcribed precursor ribosomal RNA (...
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Reposted by niels-fischer.bsky.social
Bronwyn Lucas @bronwynalucas.bsky.social · 25/07/2026
New preprint from the lab! Led by graduate student @lainahall.bsky.social we show a new method to thin cells for cryo-EM imaging with minimal damage. www.biorxiv.org/content/10.6...
biorxiv.org
Optimized cryo-FIB milling strategy to generate thin, minimally damaged biological lamellae
Focused ion beam (FIB)-milling has been adapted to thin frozen cells for visualization of macromolecular structures in situ with cryogenic electron microscopy. However, only a few large and abundant c...
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Reposted by niels-fischer.bsky.social
Florent Waltz @florentwaltz.bsky.social · 27/07/2026
This story is now published in @natplants.nature.com ! 🎉🎩 Check out the final article here: nature.com/articles/s41477-026-02361-1 Very similar to the original bioRxiv preprint, with the addition of some cool polysome analysis (in the supplementals)! Thanks and congrats to everyone involved! 🙏
nature.com
Chloroplast-encoded small subunit extensions reshape the Chlamydomonas chlororibosome - Nature Plants
Using in situ cryo-electron tomography, researchers found a unique ‘arm’ domain on the small subunit of Chlamydomonas chlororibosomes. This discovery suggests that chlororibosome structure is more evo...
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Reposted by niels-fischer.bsky.social
Misha Kudryashev @mishakudryashev.bsky.social · 01/08/2026
Take a look at our new paper on the structure of the EHD2 that, upon oligomerization, forms rings that remodel the plasma membrane and form caveolae. Beautiful work by Elena, Vasya @vasiliimikirtumov.bsky.social, Jeff & Oliver Dumke's team; take a look: www.nature.com/articles/s41...
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Reposted by niels-fischer.bsky.social
Biohub @biohub.org · 11/06/2026
In a series of 3 papers and preprints, we’re thrilled to share with you the working laser phase plate. In collaboration with research led by Holger Müller at UC Berkeley, this is a huge innovation in imaging to make small and faint objects inside cells visible. bit.ly/4vK9LVn
Waves of laser light coming from four different directions and meeting in the middle brightly inside the cavity of the laser phase plate
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niels-fischer.bsky.social @niels-fischer.bsky.social · 28/05/2026
“Speed bumps” for mitoribosomes! Our joint MPI-NAT/UMG press release highlights the story behind our NSMB paper: Mitochondrial ribosomes slow down at defined positions while newly made membrane proteins fold and enter the inner mitochondrial membrane. #Mitochondria #CryoEM #Ribosome
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Reposted by niels-fischer.bsky.social
Maximilian Madern @maxmadern.bsky.social · 20/01/2026
Excited to share our new paper! We developed a method to visualize proteasomal degradation at the single–molecule level in live cells, enabling us to dissect distinct modes of substrate engagement, probe co-factor dependence, and study proteasome–ribosome collisions. www.biorxiv.org/content/10.6...
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Reposted by niels-fischer.bsky.social
Marvin Tanenbaum @marvintanenbaum.bsky.social · 12/02/2026
Out now in Cell Systems: We develop a technique to visualize influenza A virus in live cells with single viral RNA resolution. Combined with precise readouts of viral transcription, we map the whole influenza A viral life cycle and identify key bottlenecks in infection. www.cell.com/cell-systems...
cell.com
Live-cell single-vRNP imaging identifies viral gene expression signatures that shape influenza infection heterogeneity
In this study, an imaging technology, “VISUN,” is developed that allows live-cell visualization of unmodified influenza virus during infection with single-vRNP resolution. Combining VISUN with multipl...
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niels-fischer.bsky.social @niels-fischer.bsky.social · 13/05/2026
How does a scanning ribosome decide where to start protein synthesis? In our new bioRxiv preprint, we identify an extended translation initiation sequence, the eTIS, an ~80-nt region around the start codon that shapes initiation efficiency: www.biorxiv.org/content/10.6... #Ribosome #CryoEM #mRNA
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Reposted by niels-fischer.bsky.social
Bram Verhagen @bramverhagen.bsky.social · 13/05/2026
Happy to share our preprint! Using massively parallel reporter assays, single-molecule imaging, deep learning and cryo-EM, we decode the sequence requirements for translation initiation and describe the “extended translation initiation sequence” (eTIS) that modulates start codon recognition. 🧵👇
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Reposted by niels-fischer.bsky.social
Elias Adriaenssens @elias-adriaenssens.bsky.social · 25/07/2025
And it's out! I'm thrilled to share our new paper (Adriaenssens et al., Nat Cell Biol 2025). This paper describes a new mechanism for the initiation of autophagosome biogenesis. We found that this WIPI-ATG13-driven pathway is preferentially used by a group of transmembrane autophagy receptors.
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niels-fischer.bsky.social @niels-fischer.bsky.social · 07/05/2026
How do mitochondrial ribosomes keep pace with membrane insertion? Now out in NSMB: We show that mitoribosomes slow down at defined positions linked to membrane insertion and protein topology: rdcu.be/fhqIT #Mitochondria #Ribosome #CryoEM
rdcu.be
Membrane insertion of mitochondrial-encoded proteins regulates ribosome decoding speed
Nature Structural & Molecular Biology - Schöndorf and Petrychenko et al. show that mitochondrial translation speed is coupled to OXA1L-mediated inner membrane insertion, with...
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