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小牛皮层苯二氮䓬结合位点特性的研究。

Studies on the properties of benzodiazepine-binding sites from calf cortex.

作者信息

Dudai Y, Sherman-Gold R

出版信息

Prog Biochem Pharmacol. 1980;16:95-108.

PMID:6108569
Abstract

[3H]Flunitrazepam ([3H]FNZ) specifically binds to a single class of sites in calf cortex homogenate at a level of about 1 pmol/mg protein. Essentially all binding sites sediment after a 30 min centrifugation at 20,000 X g. The affinity of the sites decreases with increasing temperature both in a homogenate and in a washed membranes preparation. Binding sites in the washed membranes preparation display lower affinity than those in the homogenate (e.g., KD of 14.8 nM vs. 7.6 nM respectively at 37 degrees C), but membrane-sites affinity can be increased by aliquots of high-speed supernatant as well as by GABA (> 10(-7) M). GABA has only a small effect on the on-reaction but slows the off-reaction. The binding sites require chloride ions (approximately 100 mM) for optimal activity, are inhibited by Hg+2, and are partially released into a high-speed supernatant by several detergents.

摘要

[3H]氟硝西泮([3H]FNZ)特异性结合小牛皮层匀浆中一类位点,结合水平约为1皮摩尔/毫克蛋白质。在20,000×g下离心30分钟后,基本上所有结合位点都会沉淀。无论是在匀浆还是在洗涤过的膜制剂中,这些位点的亲和力都随温度升高而降低。洗涤过的膜制剂中的结合位点比匀浆中的结合位点亲和力更低(例如,在37℃时,KD分别为14.8 nM和7.6 nM),但膜位点的亲和力可通过加入高速上清液等分试样以及γ-氨基丁酸(>10^(-7) M)来提高。γ-氨基丁酸对结合反应的起始阶段影响较小,但会减缓解离反应。这些结合位点需要氯离子(约100 mM)以实现最佳活性,会被Hg+2抑制,并会被几种去污剂部分释放到高速上清液中。

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