首页> 美国卫生研究院文献>Biochemical Journal >Trafficking of Kv1.4 potassium channels: interdependence of a pore region determinant and a cytoplasmic C-terminal VXXSL determinant in regulating cell-surface trafficking.
【2h】

Trafficking of Kv1.4 potassium channels: interdependence of a pore region determinant and a cytoplasmic C-terminal VXXSL determinant in regulating cell-surface trafficking.

机译:Kv1.4钾通道的贩运:孔区域决定因素和细胞质C端VXXSL决定因素在调节细胞表面运输中的相互依赖性。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Kv1.4 and Kv1.1 potassium channel homomers have been shown to exhibit different intracellular trafficking programmes and cell-surface expression levels in cell lines: a determinant in the pore region of Kv1.4 and Kv1.1 [Zhu, Watanabe, Gomez and Thornhill (2001) J. Biol. Chem. 276, 39419-39427] and a cytoplasmic C-terminal VXXSL determinant on Kv1.4 [Li, Takimoto and Levitan (2000) J. Biol. Chem. 275, 11597-11602] have been described, which affected trafficking and cell-surface expression levels. In the present study, we examined whether trafficking pore determinants influenced any cytoplasmic C-terminal trafficking determinant. We found that removal of VXXSL from a Kv1.4 chimaera that contained the pore of Kv1.1 did not affect cell-surface trafficking. Therefore removal of the C-terminal VXXSL of Kv1.4 inhibited protein surface levels only in the presence of the Kv1.4 pore. In contrast, truncating the cytoplasmic C-terminus of Kv1.1 or truncating a Kv1.1 chimaera with the pore of Kv1.4, had little effect on surface protein levels. Furthermore, the subregion of the Kv1.4 pore trafficking determinant that was required for the inhibitory effect of VXXSL removal was mapped to a threonine residue in the deep pore region. Therefore the Kv1.4 pore determinant affected the trafficking and cell-surface levels directed by the C-terminal VXXSL determinant. Different Kv1 trafficking programmes would affect cell-surface expression levels either positively or negatively and also cell signalling. Cells may use differential trafficking programmes of membrane proteins as a post-translational mechanism to regulate surface protein levels and cell function.
机译:已显示Kv1.4和Kv1.1钾通道同源物在细胞系中表现出不同的细胞内运输程序和细胞表面表达水平:Kv1.4和Kv1.1孔区域的决定因素[Zhu,Watanabe,Gomez and Thornhill(2001)J.Biol。化学276,39419-39427]和Kv1.4上的胞质C端VXXSL决定簇[Li,Takimoto and Levitan(2000)J.化学[275,11597-11602]已经描述,其影响运输和细胞表面表达水平。在本研究中,我们检查了运输孔决定因素是否影响任何细胞质C端运输决定因素。我们发现,从包含Kv1.1孔的Kv1.4嵌合体中去除VXXSL不会影响细胞表面运输。因此,仅在存在Kv1.4孔的情况下,去除Kv1.4的C端VXXSL才能抑制蛋白质表面水平。相反,截短Kv1.1的胞质C末端或截短Kv1.4的孔的Kv1.1嵌合体对表面蛋白水平影响很小。此外,将抑制VXXSL去除所需的Kv1.4孔运输决定簇的子区域映射到深孔区域的苏氨酸残基。因此,Kv1.4孔决定簇影响了C末端VXXSL决定簇指导的运输和细胞表面水平。不同的Kv1贩运计划将正面或负面地影响细胞表面表达水平,并影响细胞信号传导。细胞可以使用膜蛋白的差异运输程序作为翻译后机制来调节表面蛋白水平和细胞功能。

著录项

相似文献

  • 外文文献
  • 中文文献
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号