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亲环毒素的光敏类似物对使君子氨酸敏感的谷氨酸受体的失活作用

Inactivation of a quisqualate-sensitive glutamate receptor by photosensitive analogues of philanthotoxin.

作者信息

Goodnow R A, Nakanishi K, Sudan H L, Usherwood P N

机构信息

Department of Chemistry, Columbia University, New York, NY.

出版信息

Neurosci Lett. 1991 Apr 15;125(1):62-4. doi: 10.1016/0304-3940(91)90131-c.

Abstract

Three photosensitive, synthetic analogues of delta-philanthotoxin (PhTX-433) have been tested on the locust, excitatory nerve-muscle system. At 10(-9) M they inhibit reversibly the postjunctional currents (EPSCs) recorded from muscle fibres during motor nerve stimulation, mainly by non-competitively antagonizing postjunctional quisqualate-sensitive glutamate receptors (Quis-R), probably through open channel block. This use-dependent antagonism is characteristic of the philanthotoxins. When the preparation was irradiated with 270 nm U.V. during toxin application and nerve stimulation the EPSCs were inhibited irreversibly. Irradiation of the preparation alone or in the presence of philanthotoxins (e.g. PhTX-433) which are not photosensitive did not lead to irreversible inhibition of the EPSC. It is concluded that the three photosensitive toxins bind covalently to Quis-R in its open channel conformation during U.V. irradiation, thereby irreversibly blocking the channel gated by this receptor.

摘要

已对三种δ- philanthotoxin(PhTX - 433)的光敏合成类似物在蝗虫兴奋性神经肌肉系统上进行了测试。在10^(-9) M浓度下,它们可逆地抑制运动神经刺激期间从肌肉纤维记录到的接头后电流(EPSCs),主要是通过非竞争性拮抗接头后quisqualate敏感型谷氨酸受体(Quis - R),可能是通过开放通道阻断。这种使用依赖性拮抗作用是 philanthotoxins 的特征。当在毒素应用和神经刺激期间用270 nm紫外线照射标本时,EPSCs 被不可逆地抑制。单独照射标本或在存在非光敏的 philanthotoxins(例如 PhTX - 433)的情况下照射,均不会导致 EPSC 的不可逆抑制。得出的结论是,在紫外线照射期间,这三种光敏毒素以开放通道构象与 Quis - R 共价结合,从而不可逆地阻断该受体门控的通道。

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