Laboratoire d'Innovation Thérapeutique, UMR7200 CNRS/Université de Strasbourg, Strasbourg Drug Discovery and Development Institute (IMS), 74 route du Rhin, 67401 Illkirch-Graffenstaden, France.
Plate-forme de chimie biologique intégrative de Strasbourg (PCBiS), UMS 3286 CNRS/Université de Strasbourg, Strasbourg Drug Discovery and Development Institute (IMS), ESBS Pôle API, Bld Sébastien Brant, 67412 Illkirch-Graffenstaden, France.
ACS Chem Biol. 2021 Apr 16;16(4):651-660. doi: 10.1021/acschembio.0c00897. Epub 2021 Mar 18.
The local lipid microenvironment of transmembrane receptors is an essential factor in G protein coupled receptor (GPCR) signaling. However, tools are currently missing for studying endogenously expressed GPCRs in primary cells and tissues. Here, we introduce fluorescent environment-sensitive GPCR ligands for probing the microenvironment of the receptor in living cells using fluorescence microscopy under no-wash conditions. We designed and synthesized antagonist ligands of the oxytocin receptor (OTR) by conjugating a high-affinity nonpeptidic OTR ligand PF-3274167 to the environment-sensitive fluorescent dye Nile Red. The length of the polar PEG spacer between the pharmacophore and the fluorophore was adjusted to lower the nonspecific interactions of the probe while preserving a strong fluorogenic response. We demonstrated that the new probes embed into the lipid bilayer in the vicinity of the receptor and convey information about the local polarity and the lipid order via the wavelength-shifting emission of the Nile Red fluorophore.
跨膜受体的局部脂质微环境是 G 蛋白偶联受体 (GPCR) 信号转导的一个重要因素。然而,目前还缺乏用于研究原代细胞和组织中内源性表达的 GPCR 的工具。在这里,我们引入了荧光环境敏感的 GPCR 配体,用于在无洗涤条件下使用荧光显微镜研究活细胞中受体的微环境。我们通过将高亲和力非肽 OT 受体 (OTR) 配体 PF-3274167 偶联到环境敏感的荧光染料尼罗红,设计并合成了 OTR 的拮抗剂配体。在药效团和荧光团之间的极性 PEG 间隔臂的长度进行了调整,以降低探针的非特异性相互作用,同时保持强荧光响应。我们证明,新的探针嵌入受体附近的脂质双层中,并通过尼罗红荧光团的波长移动发射传递有关局部极性和脂质有序性的信息。