Müller Christa E, Baqi Younis, Namasivayam Vigneshwaran
PharmaCenter Bonn, Pharmaceutical Institute, Pharmaceutical & Medicinal Chemistry, University of Bonn, Bonn, Germany.
Department of Chemistry, Sultan Qaboos University, Muscat, Oman.
Methods Mol Biol. 2020;2041:45-64. doi: 10.1007/978-1-4939-9717-6_3.
Membrane receptors that are activated by the purine nucleoside adenosine (adenosine receptors) or by purine or pyrimidine nucleotides (P2Y and P2X receptors) transduce extracellular signals to the cytosol. They play important roles in physiology and disease. The G protein-coupled adenosine receptors comprise four subtypes: A, A, A, and A. The G-protein-coupled P2Y receptors are subdivided into eight subtypes: P2Y, P2Y, P2Y, P2Y, P2Y, P2Y, P2Y, and P2Y, while the P2X receptors represent ATP-gated homomeric or heteromeric ion channels consisting of three subunits; the most important subunits are P2X1, P2X2, P2X3, P2X4, and P2X7. This chapter provides guidance for selecting suitable tool compounds for studying these large and important purine receptor families.
被嘌呤核苷腺苷(腺苷受体)或嘌呤或嘧啶核苷酸(P2Y和P2X受体)激活的膜受体将细胞外信号转导至细胞质。它们在生理和疾病中发挥重要作用。G蛋白偶联腺苷受体包括四种亚型:A1、A2、A3和A4。G蛋白偶联P2Y受体细分为八种亚型:P2Y1、P2Y2、P2Y4、P2Y6、P2Y11、P2Y12、P2Y13和P2Y14,而P2X受体代表由三个亚基组成的ATP门控同聚体或异聚体离子通道;最重要的亚基是P2X1、P2X2、P2X3、P2X4和P2X7。本章为研究这些庞大且重要的嘌呤受体家族选择合适的工具化合物提供指导。