Shimazaki K, Hagiwara K, Hirata Y, Nakajima T, Kawai N
Department of Neurobiology, Tokyo Metropolitan Institute for Neurosciences, Japan.
Neurosci Lett. 1988 Jan 22;84(2):173-7. doi: 10.1016/0304-3940(88)90403-x.
Distribution of the binding sites of Joro spider toxin (JSTX), a specific inhibitor of the glutamate receptors in the crustacean neuromuscular synapse, was studied by using autoradiography. JSTX was synthesized and made radioactive by conjugation with iodine-125. 125I-JSTX irreversibly blocked the excitatory postsynaptic potentials of the lobster neuromuscular synapse in a similar manner as the natural spider toxin. Light microscopic autoradiography of 125I-JSTX treated muscle showed sporadic aggregates of reduced silver grains on the surface of muscles. Electron microscopy of adjoining ultrathin sections revealed that these spots corresponded to the fraction of sarcolemma apposed to axonal terminals with or without synaptic junctional profiles. This finding gives morphological support to the formulation that JSTX binds to the glutamate receptor-ion channel molecules.
利用放射自显影技术研究了龙虾神经肌肉突触中谷氨酸受体特异性抑制剂——乔罗蜘蛛毒素(JSTX)结合位点的分布情况。通过与碘-125结合,合成并标记了放射性的JSTX。125I-JSTX以与天然蜘蛛毒素相似的方式不可逆地阻断了龙虾神经肌肉突触的兴奋性突触后电位。对经125I-JSTX处理的肌肉进行光学显微镜放射自显影显示,肌肉表面有散在的银颗粒减少的聚集区。相邻超薄切片的电子显微镜观察表明,这些位点对应于与有或无突触连接结构的轴突终末相对的肌膜部分。这一发现为JSTX与谷氨酸受体离子通道分子结合的假说提供了形态学支持。