Zhao Qi, Ran Xu-Qin, Yan Zhu-Ying, Qian Hai-Long, Yan Xiu-Ping
State Key Laboratory of Food Science and Resources, Jiangnan University, Wuxi, 214122, China.
International Joint Laboratory on Food Safety, Jiangnan University, Wuxi, 214122, China.
Nat Commun. 2025 Feb 20;16(1):1820. doi: 10.1038/s41467-025-57064-6.
Histamine receptor, one typical G-protein-coupled receptor (GPCR), can be activated by histamine and form the most important drug targets involved in allergy and reflux diseases. Here, we report an artificial model to mimic the wettability-induced activation of natural GPCRs via histamine-modulated enhancement of wettability in a bionic nanochannel. The artificial receptor is constructed by introducing key recognition factors in nature, L-lysine modified fluorescein isothiocyanate (L-lysine-FITC), into a conical nanochannel. The conductance of the L-lysine-FITC-modified nanochannel increases with the histamine-induced wettability enhancement due to the various interactions between histamine and L-lysine-FITC molecules including hydrogen bonding and π-π interactions, as well as the proton transfer reaction. This study represents a crucial step towards the design of artificial GPCRs with wettability-induced activation and provides an opportunity to construct artificial models of GPCRs in a non-lipid environment. The developed artificial receptor has great potential application in medicinal chemistry, biosensors, and healthcare systems.
组胺受体是一种典型的G蛋白偶联受体(GPCR),可被组胺激活,并构成过敏和反流疾病中最重要的药物靶点。在此,我们报告了一种人工模型,该模型通过仿生纳米通道中组胺调节的润湿性增强来模拟天然GPCR的润湿性诱导激活。通过将自然界中的关键识别因子L-赖氨酸修饰的异硫氰酸荧光素(L-赖氨酸-FITC)引入锥形纳米通道来构建人工受体。由于组胺与L-赖氨酸-FITC分子之间存在包括氢键和π-π相互作用以及质子转移反应在内的各种相互作用,L-赖氨酸-FITC修饰的纳米通道的电导率随着组胺诱导的润湿性增强而增加。这项研究是设计具有润湿性诱导激活的人工GPCR的关键一步,并为在非脂质环境中构建GPCR的人工模型提供了机会。所开发的人工受体在药物化学、生物传感器和医疗保健系统中具有巨大的潜在应用价值。