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Poly-L-glutamine forms cation channels: relevance to the pathogenesis of the polyglutamine diseases.

机译:聚-L-谷氨酰胺形成阳离子通道:与聚谷氨酰胺疾病的发病机理有关。

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摘要

We report that long-chain poly-L-glutamine forms cation-selective channels when incorporated into artificial planar lipid bilayer membranes. The channel was permeable to alkali cations and H(+) ions and virtually impermeable to anions; the selectivity sequence based on the single-channel conductance was H(+) >> Cs(+) > K(+) > Na(+). The cation channel was characterized by long-lived open states (often lasting for several minutes to tens of minutes) interrupted by brief closings. The appearance of the channel depended critically on the length of polyglutamine chains; ion channels were observed with 40-residue stretches, whereas no significant conductance changes were detected with 29-residue tracts. The channel-forming threshold length of poly-L-glutamine was thus between 29 and 40 residues. A molecular mechanics calculation suggests a mu-helix (. Biophys. J. 69:1130-1141) as a candidate molecular structure of the channel. The channel-forming nature of long-chain poly-L-glutamine may provide a clue to the elucidation of the pathogenetic mechanism of the polyglutamine diseases, a group of inherited neurodegenerative disorders including Huntington's disease.
机译:我们报告说,当掺入人工平面脂质双层膜时,长链聚-L-谷氨酰胺形成阳离子选择性通道。该通道可渗透碱金属阳离子和H(+)离子,而几乎不渗透阴离子。基于单通道电导的选择性序列为H(+) Cs(+)> K(+)> Na(+)。阳离子通道的特征是长期处于打开状态(通常持续数分钟至数十分钟),并被短暂的关闭打断。通道的出现关键取决于聚谷氨酰胺链的长度。在40个残基的拉伸中观察到离子通道,而在29个残基的通道中未检测到明显的电导变化。因此,聚-L-谷氨酰胺的通道形成阈值长度在29至40个残基之间。分子力学计算表明,mu-螺旋(。Biophys。J. 69:1130-1141)作为通道的候选分子结构。长链聚-L-谷氨酰胺的通道形成性质可以为阐明聚谷氨酰胺疾病的发病机理提供线索,聚谷氨酰胺疾病是包括亨廷顿氏病在内的一组遗传性神经退行性疾病。

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