Giraudat J, Gali J, Revah F, Changeux J, Haumont P, Lederer F
URA CNRS 0210, Départment des Biotechnologies, Institut Pasteur, Paris, France.
FEBS Lett. 1989 Aug 14;253(1-2):190-8. doi: 10.1016/0014-5793(89)80957-3.
The membrane bound acetylcholine receptor from Torpedo marmorata was photolabeled by the noncompetitive channel blocker ]3H]chlorpromazine under equilibrium conditions in the presence of the agonist carbamoylcholine. The radioactivity incorporated into the AChR subunits was reduced by addition of phencyclidine, a specific ligand for the high-affinity side for noncompetitive blockers. The alpha-subunit was purified and digested with trypsin and/or CNBr and the resulting fragments fractionated by HPLC. Sequence analysis resulted in the identification of Ser-248 as a major residue labeled by [3H]chlorpromazine in a phencyclidine-sensitive manner. This residue is located in the hydrophobic and putative transmembrane segment M2 of the alpha-subunit, a region homologous to that containing the chlorpromazine-labeled Ser-262 in the delta-chain [1] and Ser-254 and Leu-257 in the beta-chain [2]. Extended sequence analysis of the hydrophobic segment M1 further showed that no labeling-occurred in this region.
在激动剂氨甲酰胆碱存在的平衡条件下,用非竞争性通道阻滞剂[³H]氯丙嗪对电鳐的膜结合型乙酰胆碱受体进行光标记。加入苯环己哌啶(一种非竞争性阻滞剂高亲和力位点的特异性配体)后,掺入乙酰胆碱受体亚基的放射性降低。纯化α亚基并用胰蛋白酶和/或溴化氰消化,所得片段通过高效液相色谱法进行分离。序列分析确定Ser-248是以苯环己哌啶敏感的方式被[³H]氯丙嗪标记的主要残基。该残基位于α亚基的疏水且假定的跨膜片段M2中,该区域与δ链中含氯丙嗪标记的Ser-262[1]以及β链中Ser-254和Leu-257的区域同源。对疏水片段M1的进一步序列分析表明该区域未发生标记。