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红细胞膜的水交换:生物化学和核磁共振研究重新评估巯基试剂和蛋白水解酶对人膜的影响。

Water exchange through erythrocyte membranes: biochemical and nuclear magnetic resonance studies re-evaluating the effects of sulfhydryl reagents and of proteolytic enzymes on human membranes.

作者信息

Benga G, Popescu O, Borza V, Pop V I, Hodârnău A

机构信息

Department of Cell Biology, Faculty of Medicine, Medical and Pharmaceutical Institute Cluj-Napoca, Roumania.

出版信息

J Membr Biol. 1989 May;108(2):105-13. doi: 10.1007/BF01871022.

Abstract

The water permeability of human red blood cell (RBC) membrane has been monitored by a doping nuclear magnetic resonance (NMR) technique on intact cells and resealed ghosts following exposure to various sulfhydryl-reacting (SH) reagents and proteolytic enzymes. The main conclusions are the following: (i) When appropriate conditions for exposure of erythrocytes or ghosts to mercury-containing SH reagents (concentration, temperature and duration of incubation) were found, the maximal inhibition of water diffusion could be obtained with all mercurials (including HgCl2 and mersalyl that failed to show their inhibitory action on RBC water permeability in some investigations). While previous studies claimed that long incubation times are required for the development of maximal inhibition of water diffusion by mercurials, the present results show that it can be induced in a much shorter time (5-15 min at 37 degrees C) if relatively high concentrations of PCMBS (2-4 mM) are used and no washings of the inhibitor are performed after incubation. Higher than optimal concentrations of mercurials and/or longer incubation times result in lower values of inhibition, sometimes a loss of inhibition, or can even lead to higher values of permeability compared to control RBCs. (ii) The conditions for inhibition by mercurials are drastically changed by preincubation of erythrocytes with noninhibitory SH reagents (such as NEM or IAM) or by exposure to proteolytic enzymes. If the cells are digested with papain, the duration of incubation with PCMBS should be decreased in order for inhibition to occur. This explains the lack of inhibition reported previously, when a relatively long duration of incubation with PCMBS was used subsequent to papain digestion.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过掺杂核磁共振(NMR)技术,在完整细胞以及暴露于各种巯基反应(SH)试剂和蛋白水解酶后重新封闭的血影上,监测了人类红细胞(RBC)膜的水渗透性。主要结论如下:(i)当找到红细胞或血影暴露于含汞SH试剂的合适条件(浓度、温度和孵育持续时间)时,所有汞剂(包括在一些研究中未能显示对RBC水渗透性有抑制作用的HgCl2和汞撒利)都能获得最大程度的水扩散抑制。虽然先前的研究声称汞剂对水扩散的最大抑制作用需要较长的孵育时间,但目前的结果表明,如果使用相对高浓度的对氯汞苯甲酸(PCMBS,2 - 4 mM)且孵育后不洗涤抑制剂,在更短的时间(37℃下5 - 15分钟)内就能诱导出这种抑制作用。高于最佳浓度的汞剂和/或更长的孵育时间会导致较低的抑制值,有时抑制作用丧失,甚至与对照RBC相比导致更高的渗透性值。(ii)红细胞预先用非抑制性SH试剂(如N - 乙基马来酰亚胺或碘乙酰胺)孵育或暴露于蛋白水解酶后,汞剂的抑制条件会发生剧烈变化。如果用木瓜蛋白酶消化细胞,为了产生抑制作用,与PCMBS的孵育时间应缩短。这解释了先前报道的在木瓜蛋白酶消化后使用相对较长时间的PCMBS孵育时缺乏抑制作用的原因。(摘要截于250字)

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