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蜘蛛毒液可抑制L-谷氨酸与脑突触膜受体的结合。

Spider venoms inhibit L-glutamate binding to brain synaptic membrane receptors.

作者信息

Michaelis E K, Galton N, Early S L

出版信息

Proc Natl Acad Sci U S A. 1984 Sep;81(17):5571-4. doi: 10.1073/pnas.81.17.5571.

Abstract

The venoms from three spider species, Araneus gemma, Neoscona arabesca, and Argiope aurantia, were shown to inhibit the high-affinity, sodium-independent L-glutamate-binding sites in rat brain synaptic membranes. The same three venoms caused concentration-dependent inhibition of the activity of the glutamate-binding glycoprotein purified from rat brain synaptic membranes. The venom milked from the glands of Araneus gemma was the most active inhibitor of L-glutamate binding, causing 60-80% inhibition of both synaptic membrane and purified protein binding activity at 0.01 unit. The inhibitory activity of this venom was associated with a single protein peak obtained from gel permeation chromatography of the venom. Finally, the effect of the venom from Araneus gemma on the synaptic membrane glutamate-binding sites was slowly reversible. These observations indicate that the spider venoms have a direct effect on the recognition sites for L-glutamic acid in brain synaptic membranes and that these sites are related to the physiologic glutamate receptors.

摘要

研究表明,球腹蛛、横纹金蛛和金蛛这三种蜘蛛的毒液能够抑制大鼠脑突触膜中高亲和力、不依赖钠的L-谷氨酸结合位点。同样这三种毒液对从大鼠脑突触膜中纯化得到的谷氨酸结合糖蛋白的活性产生浓度依赖性抑制作用。从球腹蛛腺体采集的毒液是L-谷氨酸结合的最有效抑制剂,在0.01单位时可导致突触膜和纯化蛋白结合活性60%-80%的抑制。这种毒液的抑制活性与毒液经凝胶渗透色谱法得到的单一蛋白峰相关。最后,球腹蛛毒液对突触膜谷氨酸结合位点的作用是缓慢可逆的。这些观察结果表明,蜘蛛毒液对脑突触膜中L-谷氨酸的识别位点有直接作用,且这些位点与生理性谷氨酸受体相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd07/391748/ce6e860768cc/pnas00618-0300-a.jpg

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