ChemUniCologne

@chemunicologne.bsky.social

Official account of the Department of Chemistry and Biochemistry at the University of Cologne, sharing news about teaching and research. To learn more please visit https://chemie.uni-koeln.de/.

🎉Important day for our Department! The construction of the new building for Chemistry and for Teacher Education is progressing at pace. Completion of the first part is anticipated for 2029🤞, enabling research and teaching in close proximity. And it already looks FANTASTIC!

Universität zu Köln@unicologne.bsky.social · 2mo ago

⚗️🧪 Universität zu Köln legt Grundstein der neuen Chemie Heute, am 1. Juni, wurde der Grundstein für die Neubauten der Chemischen Institute für die Bereiche Chemie und Biochemie und der Didaktiken in einem feierlichen Akt gelegt. Mehr dazu ▶️ uni.koeln/EX7YJ #uniköln #unicologne #unibaut #chemie

Fünf Personen stehen bei einer Grundsteinlegung vor einem Steinblock mit der Aufschrift „GRUNDSTEIN 01.06.2026“ auf einer Baustelle.

Congratulations @gabriellapetti.bsky.social and @teamthomma.bsky.social on this fantastic study! It has been a pleasure collaborating with you, and we are very happy to have contributed with #NMR to such an exciting project. We truly enjoyed working together with you!

Gabriella Petti@gabriellapetti.bsky.social · 2mo ago

Excited to share our latest study with @nicksnelders.bsky.social and @teamthomma.bsky.social! We uncover the mode of action of the V. dahliae antimicrobial effector Ave1 and show that it binds LTA and disrupts bacterial membranes 🦠 www.biorxiv.org/cgi/content/...

Many thanks again for the great collaboration @gabriellapetti.bsky.social and @teamthomma.bsky.social!

Team Thomma@teamthomma.bsky.social · 2mo ago

📣Last week another @biorxivpreprint.bsky.social dropped: "A fungal pathogen effector that shapes host plant microbiota kills bacteria through lipoteichoic acid binding and membrane disruption" a joint effort by @nicksnelders.bsky.social & @gabriellapetti.bsky.social www.biorxiv.org/content/10.6...

📣 Looking for a #PhD position in #organic #electronics, #molecular #templates or #optoelectronic devices? Then check out the new funding round of the research training group TIDE! Up to 13 projects available 👇

TIDE (RTG 2591)@tide-rtg.bsky.social · 3mo ago

The #DFG funded TIDE RTG invites applications for up to 13 #PhDPositions starting in April 2027 across the @unicologne.bsky.social, @unibonn.bsky.social, and @uni-wuppertal.bsky.social. Learn more and apply: tide.uni-koeln.de/open-positions jobportal.uni-koeln.de/bewerben/2616 #PhD #Hiring #jobs

Graphic announcing PhD opportunities in the DFG-funded Research Training Group “Template-Designed Organic Electronics (TIDE).” The post advertises up to 13 PhD positions starting in April 2027 in interdisciplinary research areas including organic synthesis, interface science, device physics, ultrafast spectroscopy, and quantum chemical modelling across the Universities of Cologne, Bonn, and Wuppertal.

New publication from the lab of Prof. Mathur: "Mannose-Conjugation Resolves the Efficiency–Toxicity Trade-Off in Amine Functionalized Silica Nanocarriers via Tunable pH-Responsive Drug Release" pubs.acs.org/doi/full/10....

Mannose-Conjugation Resolves the Efficiency–Toxicity Trade-Off in Amine Functionalized Silica Nanocarriers via Tunable pH-Responsive Drug Release

Mesoporous silica nanoparticles (mSiO2–NPs) are efficient drug delivery vehicles, yet their surface chemistry critically dictates payload uptake, therapeutic efficiency, and biocompatibility. Conventional organic coatings on the surface, such as polyethylenimine (PEI), improve drug loading capacity but substantiate cytotoxicity, while inorganic coatings/surface functionalization (e.g., (3-aminopropyl)trimethoxysilane (APTMS)) grafting reduces toxicity but offers uncontrolled drug release. Here, we present the first systematic comparison of APTMS- and PEI-functionalized mSiO2, with and without mannose conjugation, to establish how sequential surface modification governs nicotinic acid (NA) loading, release kinetics, and cellular response. Using NA as a model drug, PEI-coated carriers achieved the highest loading (DEE = 83%) and sustained, pH-responsive release (41% in 24 h at pH 5.5) but displayed pronounced cytotoxicity in breast cancer cells (MCF-7) and peripheral blood mononuclear cells (PBMCs). Mannose conjugation substantially reduced this toxicity, while maintaining drug loading efficiency and enhancing cellular uptake in both epithelial and immune cell cultures. Notably, mannose-functionalized PEI carriers exhibited targeted, stimulus-sensitive release and selective enrichment in monocyte subsets without inducing immune activation, consistent with uptake mediated by carbohydrate-binding receptors confirmed via confocal colocalization analysis. These findings establish mannose coating as an effective strategy to reconcile efficiency and safety in amine-functionalized silica nanocarriers, providing a practical design principle for targeted and biocompatible drug delivery systems.

pubs.acs.org

39th "Technetium Matters" online seminar on zoom Thursday March 19th 16:00 MET Vijay Kumar (HZDR Dresden) "Pyrite solubility and its capacity to immobilize technetium-99 in metabolite-rich environments" Please send me a DM if you like to participate. 🧪

🧬🔬 A research team led by @kathlab.bsky.social has developed an artificial DNA base pair that works according to a new chemical principle. In contrast to natural bases, the novel artificial base pairs use halogen bonds that are enzymatically incorporated into DNA. Read more: ➡️ uni.koeln/AP4XF

Artificial DNA base pair developed based on halogen bonds

A research team at the University of Cologne has developed an artificial DNA base pair that works according to a new chemical principle. In contrast to natural bases, the novel artificial base pairs u...

uni.koeln

✂️ Tie off When Professor Dr Sanjay Mathur arrived in Cologne, he soon experienced a culture shock: during his first Carnival, a colleague snipped off his tie to great applause. Coming from India and having worked in Saarbrücken and Würzburg, he wasn’t prepared for this tradition ▶️ uni.koeln/VGD7X

Person in Anzug mit grün gestreifter Krawatte, umgeben von Händen, die alte Krawatten aus den Jahren 2010 bis 2023 mit Scheren abschneiden.

New paper in @jacs.acspublications.org 🎉: A de novo designed unnatural base pair that exploits halogen bonding as pairing force in DNA for genetic alphabet expansion. 🧬 ⚗️ @unicologne.bsky.social @chemunicologne.bsky.social @breugstlab.bsky.social pubs.acs.org/doi/abs/10.1...

Investigating Halogen Bonds as Pairing Force in an Artificial DNA Base Pair

The past decades have seen significant expansion of the nucleic acid space with the development of modified artificial base pairs based on natural nucleic acid analogues and even entirely new designed base pairs. This expansion has led to tremendous potential for applications such as site-specific labeling and structural investigations. However, natural nucleic acids rely strongly on hydrogen bonding as the attraction force, which has driven the development of artificial base pairs that adapt this mechanism. To achieve orthogonality with natural bases, unnatural base pairs with alternative attraction forces, such as hydrophobic interactions, have been developed which however can perturb duplex structures. Our work introduces a completely newly designed artificial base pair that leverages halogen bonding (R–Hal···) as a directional hydrogen bonding-like interaction. We report computational studies that led to the development of this novel unnatural base pair and its synthesis. Our results demonstrate the successful acceptance of a bulky iodinated nucleoside triphosphate by KlenTaq DNA polymerase, enabling the selective enzymatic synthesis of a DNA strand containing the dIIPO–doIPP base pair. Our work presents the first demonstration of a novel base pair with halogen bonding potential that is enzymatically incorporated into DNA.

pubs.acs.org