Richard Lincoln, PhD

@rlincolnchemist.bsky.social

Postdoctoral Scientist at EMBL Heidelberg | PhD #Chemistry #ChemBio @mcgillu.bsky.social | Fluorescence probes, fluorophores. 🇨🇦 he/him

📢 I'm thrilled to announce that I'll be joining the HHMI Janelia Research Campus as a Group Leader in MTI! It's an honor to be part of Janelia's Next Chapter, pushing dye development and imaging technologies into new dimensions. The Lincoln Lab launches Sept. 14th, stay tuned for more info! 🔬⚗️👨🏼‍🔬

We have introduced a new biocompatible sulfonium-based building block for generation of non-cytotoxic covalent fluorescent probes. The proof-of-concept paper is on BioRxiv: https://doi.org/10.1101/2025.01.27.635008 . Great job done by @MarieAuvray4 at @mpi_nat ! Enjoy reading!

Biocompatible sulfonium-based covalent probes for endogenous tubulin fluorescence nanoscopy in live and fixed cells

Fluorescent probes enable the visualization of dynamic cellular processes with high precision, particularly when coupled with super-resolution imaging techniques that surpass the diffraction limit. Traditional methods include fluorescent protein fusion (e.g., GFP) or organic fluorophores linked to ligands targeting the protein of interest. However, these approaches often introduce functional disruptions or ligand-associated biological effects. Herein, we address these challenges by developing covalent fluorescent probes for endogenous tubulin, a critical cytoskeletal protein involved in processes such as cell movement, division, and biomolecule trafficking. Using well-known tubulin binder cabazitaxel and cell permeable fluorophore silicon-rhodamine—as a basis, we introduce a novel biocompatible cleavable linker containing a sulfonium center. This allowed the construction of the optimized probe , 6-SiR- o -C9-CTX , demonstrating excellent cell permeability, fluorogenic properties, and the ability to covalently label tubulin across various human cell lines. Importantly, the targeting moiety could be washed out while preserving tubulin staining, ensuring minimal disruption of tubulin function. This labeling technique is compatible with STED nanoscopy in both live and fixed cells, offering a powerful high-resolution imaging tool. ### Competing Interest Statement G.L. is a co-inventor on the patent (EP2748173B1 and US9346957B2, applicant EPFL) describing SiR and its derivatives.

doi.org

Hi there! 👋 We are the PR team of the Max Planck Institute for Medical Research in beautiful Heidelberg and very excited to join Bluesky! 😍🥳 Follow us to learn more about our research, our great people, events, awards etc! We are really looking forward to interacting with you! 🚀🗨️