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短波紫外线照射可增强苯二氮䓬类位点的光亲和标记。

Short-wave ultraviolet irradiation increases photo-affinity labeling of benzodiazepine sites.

作者信息

Herblin W F, Mechem C C

出版信息

Life Sci. 1984 Jul 16;35(3):317-24. doi: 10.1016/0024-3205(84)90115-2.

Abstract

Photoaffinity labeling of benzodiazepine sites with [3H]-flunitrazepam was examined using either long-wave (366 nm) or short-wave (254 nm) ultraviolet irradiation. A multiple exposure protocol was employed so that the time course of the process could be determined as well as the fraction of total sites labeled. At 366 nm, approximately 20% of the total sites present were labeled and the remainder showed reduced affinity for flunitrazepam, in agreement with published reports. When membranes from either cortex or cerebellum were irradiated at 254 nm, however, the fraction of sites labeled increased above 40%. The change in the ratio of labeled sites to those showing reduced affinity, as well as differences in the time courses of the two phenomena, are taken as evidence that the labeling and affinity change are independent processes rather than two effects of a single event. Inhibition of labeling by clonazepam and Ro15-1788 indicated the "central" nature of the labeled sites.

摘要

使用长波(366纳米)或短波(254纳米)紫外线照射,研究了用[3H]氟硝西泮对苯二氮䓬位点进行光亲和标记。采用了多次曝光方案,以便确定该过程的时间进程以及被标记的总位点比例。在366纳米处,约20%的总位点被标记,其余位点对氟硝西泮的亲和力降低,这与已发表的报告一致。然而,当来自皮质或小脑的膜在254纳米处照射时,被标记的位点比例增加到40%以上。标记位点与亲和力降低位点的比例变化,以及这两种现象时间进程的差异,被视为标记和亲和力变化是独立过程而非单一事件的两种效应的证据。氯硝西泮和Ro15 - 1788对标记的抑制表明了被标记位点的“中心”性质。

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