首页> 外文期刊>Biochimica et biophysica acta. Biomembranes >Modification of erythrocyte Na~+/Li~+ countertransport kinetics by two types of thiol group
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Modification of erythrocyte Na~+/Li~+ countertransport kinetics by two types of thiol group

机译:两种巯基对红血球Na〜+ / Li〜+逆向传输动力学的修饰

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摘要

Erythrocyte Na?/Li+ countertransport activity is decreased by reagents that react with thiol groups. An understanding of the role of these groups in control of Na+/Li+ countertransport may help to explain its association with disease states. The effect of thiol reactive agents on the kinetic parameters of Na+/Li+ countertransport has not previously been described. In choline medium, N-ethylmaleimide (NEM) and iodoacetamide (IAamide) cause a rapid decrease of about 40% in Km for external sodium (Km(So)) that is complete in 10 s with a much smaller change in Vmax and an increase in the Vmax/Km ratio. In Na medium, NEM and IAamide both cause a rapid decrease in Km(So) and Vmax. With NEM the partial reduction in Vmax is complete in 100 s although the NEM is sufficient to reduce Vmax up to 15 min. With IAamide the decrease in Vmax is initially slower but it continues apparently towards complete inhibition. These results indicate at least two types of thiol group controlling Na+/Li+ countertransport kinetics. The type 1 thiol reaction is Na independent and causes an increase in the apparent rate constant for Na association with the unloaded carrier so that Vmax/Km rises and Km(So) decreases. The type 2 thiol reaction is facilitated by Na at the outside ion-binding site and causes a decrease in Vmax, possibly by total blockage of carriers with IAamide but by a different mechanism with NEM such as reduced turnover rate.
机译:与硫醇基反应的试剂降低了红血球Na + / Li +的逆向转运活性。了解这些组在控制Na + / Li +逆向转运中的作用可能有助于解释其与疾病状态的关系。硫醇反应剂对Na + / Li +反转运动力学参数的影响以前没有描述过。在胆碱介质中,N-乙基马来酰亚胺(NEM)和碘乙酰胺(IAamide)导致外部钠(Km(So))的Km迅速降低约40%,在10 s内完成,Vmax的变化小得多,并且增加在Vmax / Km比中在Na介质中,NEM和IAamide都会导致Km(So)和Vmax迅速下降。使用NEM,尽管NEM足以将Vmax降低至15分钟,但Vmax的部分降低会在100 s内完成。使用IAamide时,Vmax的降低起初较慢,但显然继续朝着完全抑制的方向发展。这些结果表明至少两种类型的硫醇基团控制Na + / Li +逆向传输动力学。 1型硫醇反应与Na无关,并且会导致与空载的Na缔合时Na的表观速率常数增加,从而Vmax / Km升高而Km(So)降低。在外部离子结合位点的Na促进2型硫醇反应,并导致Vmax降低,可能是由于IAamide完全阻断了载体,但与NEM产生了不同的机制,例如降低了周转率。

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