Amitai G, Avissar S, Balderman D, Sokolovsky M
Proc Natl Acad Sci U S A. 1982 Jan;79(2):243-7. doi: 10.1073/pnas.79.2.243.
Highly potent photoaffinity probes for muscarinic binding sites were prepared by the incorporation of an azido group into the benzilic acid moiety in two compound, 3-quinuclidinyl benzilate (3QNB) and N-methyl-4-piperidyl benzilate (4NMPB). Inactivation of muscarinic sites in rat cortex depends on the formation of a reversible complex with the azides prior to their photolytic conversion to the highly reactive nitrenes. During photolysis, radiolabeled azido-4NMPB interacted specifically and with high affinity (Kd = 1.06 nM) with the muscarinic receptors, and the ligand could be covalently incorporated into a macromolecule of about 86,000 Mr, presumably the muscarinic receptor. The incorporation was almost stoichiometric when compared to determination of receptor density by reversible ligands. Atropine (10 microM) afforded specific protection (greater than 83%) of the receptor against inactivation by azido-[3H]4NMPB. This compound and the other ligands described here (i.e., amino-4NMPB, amino-3QNB, and azido-3QNB) represent powerful potential probes for the biochemical isolation and characterization of muscarinic receptors.
通过将叠氮基引入两种化合物——3-喹核醇苯甲酸酯(3QNB)和N-甲基-4-哌啶醇苯甲酸酯(4NMPB)的二苯乙醇酸部分,制备了用于毒蕈碱结合位点的高效光亲和探针。大鼠皮层中毒蕈碱位点的失活取决于叠氮化物在光解转化为高反应性氮烯之前与叠氮化物形成可逆复合物。在光解过程中,放射性标记的叠氮基-4NMPB与毒蕈碱受体特异性且高亲和力地相互作用(Kd = 1.06 nM),并且配体可以共价结合到大约86,000 Mr的大分子中,推测该大分子是毒蕈碱受体。与通过可逆配体测定受体密度相比,这种结合几乎是化学计量的。阿托品(10 microM)为受体提供了针对叠氮基-[3H]4NMPB失活的特异性保护(大于83%)。该化合物以及此处描述的其他配体(即氨基-4NMPB、氨基-3QNB和叠氮基-3QNB)代表了用于毒蕈碱受体生化分离和表征的强大潜在探针。