Development of an Affinity-Based Probe to Profile Endogenous Human Adenosine A 3 Receptor Expression .
Bert L H BeerkensInge M SnijdersJoep SnoeckRongfang LiuAnton T J ToolSylvia E Le DévédecWillem JespersTaco W KuijpersGerard van WestenLaura H HeitmanAdriaan P IJzermanLaura H HeitmanPublished in: Journal of medicinal chemistry (2023)
The adenosine A 3 receptor (A 3 AR) is a G protein-coupled receptor (GPCR) that exerts immunomodulatory effects in pathophysiological conditions such as inflammation and cancer. Thus far, studies toward the downstream effects of A 3 AR activation have yielded contradictory results, thereby motivating the need for further investigations. Various chemical and biological tools have been developed for this purpose, ranging from fluorescent ligands to antibodies. Nevertheless, these probes are limited by their reversible mode of binding, relatively large size, and often low specificity. Therefore, in this work, we have developed a clickable and covalent affinity-based probe (AfBP) to target the human A 3 AR. Herein, we show validation of the synthesized AfBP in radioligand displacement, SDS-PAGE, and confocal microscopy experiments as well as utilization of the AfBP for the detection of endogenous A 3 AR expression in flow cytometry experiments. Ultimately, this AfBP will aid future studies toward the expression and function of the A 3 AR in pathologies.
Keyphrases
- living cells
- flow cytometry
- endothelial cells
- poor prognosis
- quantum dots
- binding protein
- induced pluripotent stem cells
- oxidative stress
- pluripotent stem cells
- fluorescent probe
- label free
- small molecule
- long non coding rna
- young adults
- current status
- photodynamic therapy
- fluorescence imaging
- real time pcr
- nucleic acid