ZANIN LAB

@zaninlab.bsky.social

@fau.de Excited about Cell division, Cytoskeleton dynamics, Microscopy, C. elegans, photopharmacology 💡 ♥️😎🐛🔬

Proud that our work was published in JACS! 💫🧪🧫 This was a fruitful collaboration with the @dubelab.bsky.social. A true interdisciplinary effort to build multifunctional light controllable molecules for biomedical applications and future drugs. Amazing job by Manuel Valentin and David Féval! 👏

A Multifunctional and Secure Photoresponsive Proteasome Inhibitor to Control Cell Fate

Abstract. Precise external control of biological processes represents a central interest in the life sciences. Specifically designed molecular tools are id

pubs.acs.org

New Paper Alert! 💥 Check out our next generation multifunctional proteasome inhibitor controlled by light. A versatile and customizable chem-bio tool for steering cell fate. Congratulations to David and Manuel from the @dubelab.bsky.social on this fruitful interdisciplinary collaboration! 🧪 🔬

A Multi-Functional and Secure Photoresponsive Proteasome Inhibitor | ChemRxiv

Precise external control of biological processes represents a central interest in the life sciences. Specifically designed molecular tools are ideally suited for this purpose and consequentially have found widespread applications including fundamental ...

chemrxiv.org

Künstliche Muskeln mithilfe von winzigen molekularen Maschinen herstellen: Prof. Dr. Henry Dube (FAU) möchte Materialien für völlig neue Anwendungen entwickeln. Diese könnten durch Licht gesteuert werden und programmierbar sein. Das Projekt wird mit mehr als 900.000€ gefördert: go.fau.de/1dife

Person lächelt zur Kamera; auf der rechten Bildhälfte ein Regal, in dem sich verschiedene Behältnisse befinden.

It’s a big leap forward to describe centriolar satellites in C. elegans! This will open new avenues to study their functions during development. Congratulations @tdvalilab.bsky.social and the students Zakiah Talib and @beriltiryakiler.bsky.social. Happy that the Zanin lab could contribute. 🎉

TDvaliLab@tdvalilab.bsky.social · 5mo ago

#C.elegans is about to join the 'centriolar satellites' club. Check out our new preprint #centriolarsatellites: www.biorxiv.org/content/10.6...

Thrilled to report another milestone: 900 nm photoswitching enables NIR-light detection and reversible invisible writing of high-contrast 2D and 3D displays! Check out our newest molecular photoswitch PBFT (peri-benzo[a]fluoranthenethioindigo) at ChemRxiv - doi.org/10.26434/che...

Congratulations to Tamara and Alina! 🫶🏻🎊🎉🥳 It was a pleasure to contribute to the story. If you want to learn more about how the shape and mechanical properties of centrosomes are regulated during mitosis - a must read.

TDvaliLab@tdvalilab.bsky.social · 9mo ago

Our paper on PCMD-1 and centrosome stability is finally online! Congratulations 🎉🎉🎉 to Alina and the entire team! Very proud and grateful - it was an incredible teamwork @zaninlab.bsky.social! @lifescimunich.bsky.social. If you want to read more check it out on JCB! rupress.org/jcb/article-...

Stop by at the two lab posters at the @dgz.bsky.social Meeting in Heidelberg! Esther will present Mikhail’s work on asymmetric furrow ingression and Sophia on a novel signaling pathway that positions the cleavage furrow at the right place.

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We are excited to share our latest work on the role of anillin during unilateral cytokinesis. Congratulations to Mikhail, the leading author, for his excellent work. Big thanks to the @tdvalilab.bsky.social lab for their tremendous support.

Journal of Cell Biology@jcb.org · last yr.

Lebedev et al. @zaninlab.bsky.social @fau.de show that anillin mediates unilateral #cytokinesis by blocking the effector binding site of active RhoA. rupress.org/jcb/article/... #Development #CellDivision

Happy that we could contribute to the story: From Bones to Bugs: Structure-Based Development of Raloxifene-Derived Pathoblockers That Inhibit Pyocyanin Production in Pseudomonas aeruginosa | Journal of Medicinal Chemistry pubs.acs.org/doi/full/10....

From Bones to Bugs: Structure-Based Development of Raloxifene-Derived Pathoblockers That Inhibit Pyocyanin Production in Pseudomonas aeruginosa

The human pathogen Pseudomonas aeruginosa is particularly notorious for its multiple resistance mechanisms. A new concept for anti-infectives is the “pathoblocker” approach, which targets virulence factors to disarm rather than kill pathogens and thus attenuates the development of resistance. Based on the estrogen receptor modulator raloxifene, which had previously been identified as a potential biosynthesis inhibitor of the virulence factor pyocyanin via in silico screening, analogues have been developed as pathoblockers against P. aeruginosa. These compounds reduce the production of pyocyanin by binding to the phenazine biosynthesis enzyme PhzB. Structure–activity relationships (SAR) were explored using nano differential scanning fluorimetry, isothermal titration calorimetry, and 12 X-ray cocrystal structures. Compared to raloxifene, congener 20c shows a 60-fold lower affinity for the human estrogen receptor with a 15-fold increase in pyocyanin inhibitory activity. The comprehensive structural information gathered in this study paves the way for the development of improved pathoblockers with increased potency and selectivity.

pubs.acs.org