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低钾绵羊红细胞硫醇激活的钾氯共转运体中抑制性巯基的证据。

Evidence for inhibitory SH groups in the thiol activated K:Cl cotransporter of low K sheep red blood cells.

作者信息

Ryu K H, Lauf P K

机构信息

Department of Physiology and Biophysics, Wright State University School of Medicine, Dayton, OH 45401.

出版信息

Mol Cell Biochem. 1990 Dec 20;99(2):135-40. doi: 10.1007/BF00230343.

Abstract

The monofunctional thiol reagents N-ethylmaleimide (NEM) and methyl methanethiosulfonate (MMTS) stimulate ouabain resistant (OR) electroneutral K:Cl cotransport in LK sheep red blood cells at low, but not at high concentrations. Diamide (DM), on the other hand, only stimulates OR K:Cl flux (Lauf, P.K., J. Memb. Biol. 101: 179-188, 1988). The DM stimulated K:Cl cotransport was decreased toward the control value prior to DM stimulation when NEM or MMTS were added, subsequently. The inhibitory effect was dependent on the compound's concentration and exposure time and, in the case of MMTS, was reversed upon addition of dithiothreitol (DTT). The inhibition was more prominent when NEM treatment was performed at pH 8.0 and disappeared at pH 6.0. In contrast the NEM stimulatory effect was most effective when the pH of NEM treatment was 6.0 (Bauer, J. & Lauf, P.K., J. Memb. Biol. 73: 257-261, 1983). The results suggest the existence of additional, however, inhibitory thiol groups in the already thiol-activated K:Cl cotransporter, with a different pKa value and a lower affinity for NEM or MMTS as compared to the stimulatory thiol groups. Like the activating thiols, the inhibitory sulfhydryls appeared to be inaccessible to non-penetrating thiol reagents and hence, must be located deeper within the red cell membrane.

摘要

单功能硫醇试剂N-乙基马来酰亚胺(NEM)和甲硫基磺酸甲酯(MMTS)在低浓度而非高浓度时,可刺激LK绵羊红细胞中哇巴因抗性(OR)的电中性K:Cl协同转运。另一方面,二酰胺(DM)仅刺激OR K:Cl通量(Lauf, P.K., J. Memb. Biol. 101: 179 - 188, 1988)。当随后添加NEM或MMTS时,DM刺激的K:Cl协同转运在DM刺激前朝对照值降低。抑制作用取决于化合物的浓度和暴露时间,就MMTS而言,添加二硫苏糖醇(DTT)后抑制作用可逆转。当在pH 8.0进行NEM处理时抑制作用更显著,而在pH 6.0时消失。相反,当NEM处理的pH为6.0时,NEM的刺激作用最有效(Bauer, J. & Lauf, P.K., J. Memb. Biol. 73: 257 - 261, 1983)。结果表明,在已被硫醇激活的K:Cl协同转运蛋白中存在另外的抑制性硫醇基团,其pKa值不同,与刺激性硫醇基团相比,对NEM或MMTS的亲和力较低。与激活硫醇一样,抑制性巯基似乎对非穿透性硫醇试剂不可及,因此,必定位于红细胞膜更深层。

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