Search Results

K., Gellman, S. H., Pautsch, A., Steyaert, J., Weis, W. I., & Kobilka, B. K. (2011).

biophysical fragment screening using polymer-encapsulated nanodiscs Google DeepMind And Isomorphic Labs

Gilman, A.G., G proteins: transducers of receptor-generated signals. 

In every lab, candidates fail not because they lack potency at a receptor, but because they stumble at

AI-Driven Approach to Modern Drug Discovery Arcoscreen will present in the start-up village at Future Labs

NEW Principal Investigator, In Vitro Biology NEW Associate Scientist Postdoctoral Scholar - O’Neill Lab

World Congress of Basic and Clinical Pharmacology 2026 GPCR Jobs NEW Postdoctoral Scholar - O’Neill Lab

Hannes Schihada and his lab team developed fluorescent analogues for real-time binding studies of orphan

of Glioblastoma Associate Director / Director, Clinical Operations Postdoctoral Research Associate Lab

By using two labeled ligands the transference of energy event will only happen when the adequate distance are bound to is promiscuous, it will not compromise assay integrity the same way it would in single-label

A new contributor article from our friends at Celtrays Research outlines how dual-labeled fluorescent Dual-label specificity blocks promiscuous ligand confusion Lanthanide donors + d2 acceptors = high SNR

System-Dependent Activity and Opposing Processes Partial agonists don’t wear single labels.

This applied article walks through ligand-directed labeling, SNAP/Halo tags, and fluorescent ligands Assay flexibility:  Combine self-labeling tags with quantitative readouts (e.g., TR-FRET) to expand mechanism

Flow Cytometry validation performed in the Oncological Pharmacology Laboratory of the University of Turin

Ligand-directed labelling strategies  are a newly developed way to attach a fluorescent tag to a GPCR Another strategy is the use of self-labelling tags  such as SNAP-tag and HaloTag. This provides flexibility in labelling the GPCRs but may interfere with functional activity of the receptors Fluorescence Microscopy validation performed in the ONCOMET laboratory (Health Research Institute of

they do not require complex equipment for analysis and plate readers are usually available in regular laboratories

Real-time dynamic labeling of A 2B AR. Representative confocal images of HCT116 cells pre-stained with CellTracker Green (lower panels) and labeled CAFs are labeled with CellTracker (Green), and cocultures are labeled with CELT-327 250 nM.

Because Tag-lite® is based on FRET, we have collaborated with BMG Labtech to develop an application note Assay Principle CELT-335 is a fluorescently labelled full agonist, which binds to the orthosteric site It binds to the receptor, which is labelled with Tb.

  6  Kd calculated through saturation of CELT-335 in human HEK-293T cells transiently expressing Tb-labeled Tb labelling was performed as described in Materials and Methods. Tb labelling was performed as described in Materials and Methods. Directed Evolution of O6-Alkylguanine-DNA Alkyltransferase for Applications in Protein Labeling. A General Method for the Covalent Labeling of Fusion Proteins with Small Molecules in Vivo.

theory behind the assays FA is based on measuring the change in rotational freedom of the fluorescent label equilibrium properties of CELT-419 to D3R in BBVs FA assay, the ligand must have a suitable fluorescent label For example, some assays benefit from using a more red-shifted fluorescent label or a combination of multiple labels in a single study. For example, a Cy5-labelled fluorescent ligand with the same pharmacophore is available from Celtarys

You’d be tempted to label the first “competitive” and the second “non-competitive.”

Celtarys Research develops high-quality, fluorescently labeled ligands and innovative chemical biology Their proprietary chemistry platform enables rapid generation of conjugates, such as labeled ligands,

Triple Labeling Resolves a GPCR Intermediate State by Using Three-Color Single Molecule FRET .  

An important reason for this unfavourable situation is that laboratory experiments are performed under Dave K, Gelman H, Thu CT, Guin D, Gruebele M.

Heng , Xavier Deupi , Yang Du , Brian K Kobilka Red and far-red cleavable fluorescent dyes for self-labelling obesity drug caused up to 20% weight loss after a year, with no plateau INAUGURATION OF AELIS FARMA NEW LABORATORY cryo-EM structure determination of a Family A GPCR Red and far-red cleavable fluorescent dyes for self-labelling

Rivas-Santisteban , Ana Muñoz , Jaume Lillo , Iu Raïch , Ana Rodríguez-Pérez , Gemma Navarro , José Labandeira-García

including time, financial investment, and specialised expertise, limiting accessibility for some research laboratories BioRxiv (Cold Spring Harbor Laboratory) . https://doi.org/10.1101/2024.04.17.590000 Pines, G., Fankhauser

Therefore, it’s a great molecular tool for proximity labeling approaches in living cells.  During this process, APEX2 can label proteins in the vicinity, allowing the capture of a snapshot of After the labeling reaction, the researchers purified and biotinylated proteins (those that have been labeled by APEX2) and analyzed them using quantitative proteomics such as tandem mass tags.

Updates in GPCR Research A nondestructive membrane engineering method using an amphiphilic polymer Labeling

may miss broader functional regions, while random mutagenesis generates extensive data that require labour-intensive