Maric Lab

@hmariclab.bsky.social

#EmmyNoether Lab of Hans Maric @uni-wuerzburg.de #ChemBio #Peptides #PNA #Microarrays #ChemicalProbes pharmacological targeting of #PPI #IDR #RNA http://MaricLab.com https://www.uni-wuerzburg.de/en/rvz/research-groups/maric-group/ http://bit.ly/14S4Z8k.

Thrilled to see our work on targeted #mRNA blockade using high-throughput #antisense screening, now published in Advanced Science! 🚀 A true team effort in close collaboration with the @jorg-vogel-lab.bsky.social with special credit to Popella & Danti! ASOs for the people! bsky.app/profile/gior...

Giorgia Danti@giorgiadanti.bsky.social · last yr.

First post, first paper 🤭 Proud to share with all of you our work on mRNA blocking using our own high-throughput antisense approach! doi.org/10.1002/advs... Many thanks to @hmariclab.bsky.social, @jorg-vogel-lab.bsky.social and especially Linda for the amazing collaboration 😸

Make sure not to miss our latest paper out now in #JACS - presenting eSylites - small, peptide-based probes for precise mapping of neurons, etc.! Microscale thermophoresis (MST) played a huge part in optimizing the probes structure and sequence for binding affinity. #ChemicalBiology #Synapse

Maric Lab@hmariclab.bsky.social · last yr.

🚀 Excited to share our latest work in #JACS on eSylites! —Synthetic, high-affinity #ChemicalBiology probes for #SuperResolution #Synapse visualization & precise mapping in neurons and brain slices—without the need for antibodies, tags, or transfection! 📢 Read more: pubs.acs.org/doi/10.1021/...

Super happy to see our work on eSylites finally out in #JACS introducing small peptidic probes for simplified excitatory #Synapse visualization with unprecedented resolution! Huge thanks to all authors making this possible!

Maric Lab@hmariclab.bsky.social · last yr.

🚀 Excited to share our latest work in #JACS on eSylites! —Synthetic, high-affinity #ChemicalBiology probes for #SuperResolution #Synapse visualization & precise mapping in neurons and brain slices—without the need for antibodies, tags, or transfection! 📢 Read more: pubs.acs.org/doi/10.1021/...

🚀 Excited to share our latest work in #JACS on eSylites! —Synthetic, high-affinity #ChemicalBiology probes for #SuperResolution #Synapse visualization & precise mapping in neurons and brain slices—without the need for antibodies, tags, or transfection! 📢 Read more: pubs.acs.org/doi/10.1021/...

eSylites: Synthetic Probes for Visualization and Topographic Mapping of Single Excitatory Synapses

The spatiotemporal organization of the postsynaptic density (PSD) is a fundamental determinant of synaptic transmission, information processing, and storage in the brain. The major bottleneck that prevents the direct and precise representation of the nanometer-scaled organization of excitatory glutamatergic synapses is the size of antibodies, nanobodies, and the genetically encoded fluorescent tags. Here, we introduce small, high affinity synthetic probes for simplified, high contrast visualization of excitatory synapses without the limitations of larger biomolecules. In vitro binding quantification together with microscopy-based evaluation identified eSylites, a series of fluorescent bivalent peptides comprising a dye, linker, and sequence composition that show remarkable cellular target selectivity. Applied on primary neurons or brain slices at nanomolar concentrations, eSylites specifically report PSD-95, the key orchestrator of glutamate receptor nanodomains juxtaposed to the presynaptic glutamate release sites that mediate fast synaptic transmission. The eSylite design minimizes a spatial dye offset and thereby enables visualization of PSD-95 with improved localization precision and further time-resolved discrimination. In particular, we find that individual dendritic spines can contain separate nanodomains enriched for either PSD-95 or its closest homologues, PSD-93 or SAP102. Collectively, these data establish eSylites as a broadly applicable tool for simplified excitatory synapse visualization, as well as a high-end microscopy compatible probe for resolving the PSD organization with unprecedented resolution.

pubs.acs.org

🚨 Excited to share our work @elife.bsky.social doi.org/10.7554/eLife.98827.2 on targeting Hepatitis B virus #HBV 🦠 capsid aggregation by designed molecules! #DrugDiscovery #ChemBio Thanks V Khayenko C Makbul @clemensschulte.bsky.social & @boettchercryoem.bsky.social for stunning #CryoEM visuals!

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Bettina Böttcher@boettchercryoem.bsky.social · 2y ago

Our joined effort with the the Maric Lab @hmariclab.bsky.social @uniwuerzburg.bsky.social on how to aggregate capsids of Hepatitis B virus inside cells is now out in Elife doi.org/10.7554/eLif... . #cryoEM 🧪❄️🔬

I am super happy to share our latest article entitled "Decoding the molecular interplay of CD20 and therapeutic antibodies with fast volumetric nanoscopy", now published in Science www.science.org/doi/10.1126/... It was my postdoctoral work mit @sauer-lab.bsky.social Congrats to all the co-authors!

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Julius-Maximilians-Universität Würzburg@uni-wuerzburg.de · 2y ago

Delighted to launch our activities on Bluesky with this great news: Our researchers @sauer-lab.bsky.social show in @science.org, how therapeutic #antibodies interact with B cells – thanks to an innovative method of super-resolution microscopy. Congratulations! ➡️ www.uni-wuerzburg.de/en/news-and-...

Mode of action of the new microscopy method LLS-TDI-DNA-PAINT. On the top right, the RTX antibody was visualised on a Raij-B cell: it is easy to see how it links the CD20 molecules in the membrane. Bottom right: the hedgehog-shaped appearance of a living Raji B cell after the antibody has bound. The surface protein CD45, which is homogeneously distributed on the cell surface, is also labelled in green. (Image: Arindam Ghosh / University of Würzburg)