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通过在昆虫细胞中的异源表达对来自马铃薯的内向整流钾通道SKT1进行表征。

Characterization of SKT1, an inwardly rectifying potassium channel from potato, by heterologous expression in insect cells.

作者信息

Zimmermann S, Talke I, Ehrhardt T, Nast G, Müller-Röber B

机构信息

Max-Planck-Institut für Molekulare Pflanzenphysiologie, Karl-Liebknecht-Strasse 25, Haus 20, D-14476 Golm/Potsdam, Germany.

出版信息

Plant Physiol. 1998 Mar;116(3):879-90. doi: 10.1104/pp.116.3.879.

Abstract

A cDNA encoding a novel, inwardly rectifying K+ (K+in) channel protein, SKT1, was cloned from potato (Solanum tuberosum L.). SKT1 is related to members of the AKT family of K+in channels previously identified in Arabidopsis thaliana and potato. Skt1 mRNA is most strongly expressed in leaf epidermal fragments and in roots. In electrophysiological, whole-cell, patch-clamp measurements performed on baculovirus-infected insect (Spodoptera frugiperda) cells, SKT1 was identified as a K+in channel that activates with slow kinetics by hyperpolarizing voltage pulses to more negative potentials than -60 mV. The pharmacological inhibitor Cs+, when applied externally, inhibited SKT1-mediated K+in currents half-maximally with an inhibitor concentration (IC50) of 105 microM. An almost identical high Cs+ sensitivity (IC50 = 90 microM) was found for the potato guard-cell K+in channel KST1 after expression in insect cells. SKT1 currents were reversibly activated by a shift in external pH from 6.6 to 5.5, which indicates a physiological role for pH-dependent regulation of AKT-type K+in channels. Comparative studies revealed generally higher current amplitudes for KST1-expressing cells than for SKT1-expressing insect cells, which correlated with a higher targeting efficiency of the KST1 protein to the insect cell's plasma membrane, as demonstrated by fusions to green fluorescence protein.

摘要

从马铃薯(Solanum tuberosum L.)中克隆出一个编码新型内向整流钾离子(K⁺in)通道蛋白SKT1的cDNA。SKT1与先前在拟南芥和马铃薯中鉴定出的AKT家族K⁺in通道成员相关。Skt1 mRNA在叶片表皮片段和根中表达最强。在对杆状病毒感染的昆虫(草地贪夜蛾)细胞进行的电生理全细胞膜片钳测量中,SKT1被鉴定为一种K⁺in通道,通过将电压脉冲超极化到比-60 mV更负的电位以缓慢动力学激活。当外部施加药理抑制剂Cs⁺时,它以105 μM的抑制剂浓度(IC50)半最大程度地抑制SKT1介导的K⁺in电流。在昆虫细胞中表达后,马铃薯保卫细胞K⁺in通道KST1对Cs⁺的敏感性几乎相同(IC50 = 90 μM)。SKT1电流通过外部pH从6.6变为5.5而被可逆激活,这表明pH依赖性调节AKT型K⁺in通道具有生理作用。比较研究表明,表达KST1的细胞的电流幅度通常高于表达SKT1的昆虫细胞,这与KST1蛋白对昆虫细胞质膜的更高靶向效率相关,如与绿色荧光蛋白融合所证明的那样。

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