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作为红细胞渗透系统探针的有毒化学试剂。

Toxic chemical agents as probes for permeation systems of the red blood cell.

作者信息

Rothstein A, Knauf P A

出版信息

Adv Exp Med Biol. 1977;84:319-51. doi: 10.1007/978-1-4684-3279-4_16.

Abstract

Chemical agents with different capacities to penetrate into the membrane and with different chemical reactivities can be used to gain information concerning the location of transport sites in the membrane structure and the particular functional ligands. If the agents are highly specific in their interactions and if their inhibitory effects are irreversible, they can also be used as probes to identify the transport components. Several examples are cited using the human red blood cells as a model. The anion transport system in particular has been studied by the use of nonpenetrating irreversible inhibitors, and more recently with a photoaffinity probe, NAP-taurine. In the dark the latter is transported in competition with the normal inorganic anions but after exposure to light, it becomes fixed in an irreversible bond that allows identification of the sites of its transport. It is proposed that anion transport involves a transmembrane protein of about 90,000 daltons that forms a channel through the lipid bilayer. The exchange of anions occurs via a gating mechanism containing a specific anion-binding site. Transport of water, cations and sugars may also involve similar transmembrane protein channels.

摘要

具有不同穿透膜能力和不同化学反应性的化学试剂,可用于获取有关膜结构中转运位点位置及特定功能配体的信息。如果这些试剂在相互作用中具有高度特异性,且其抑制作用是不可逆的,那么它们也可用作探针来识别转运成分。以人类红细胞为模型列举了几个例子。特别是阴离子转运系统已通过使用非穿透性不可逆抑制剂进行研究,最近还使用了光亲和探针 NAP-牛磺酸。在黑暗中,后者与正常无机阴离子竞争转运,但在光照后,它会形成不可逆的键,从而能够识别其转运位点。有人提出,阴离子转运涉及一种约90,000道尔顿的跨膜蛋白,该蛋白形成一个穿过脂质双层的通道。阴离子的交换通过包含特定阴离子结合位点的门控机制发生。水、阳离子和糖类的转运可能也涉及类似的跨膜蛋白通道。

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