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从克隆的互补脱氧核糖核酸表达的钙激活钾通道。

Calcium-activated potassium channels expressed from cloned complementary DNAs.

作者信息

Adelman J P, Shen K Z, Kavanaugh M P, Warren R A, Wu Y N, Lagrutta A, Bond C T, North R A

机构信息

Vollum Institute, Oregon Health Sciences University, Portland 97201.

出版信息

Neuron. 1992 Aug;9(2):209-16. doi: 10.1016/0896-6273(92)90160-f.

Abstract

Calcium-activated potassium channels were expressed in Xenopus oocytes by injection of RNA transcribed in vitro from complementary DNAs derived from the slo locus of Drosophila melanogaster. Many cDNAs were found that encode closely related proteins of about 1200 aa. The predicted sequences of these proteins differ by the substitution of blocks of amino acids at five identified positions within the putative intracellular region between residues 327 and 797. Excised inside-out membrane patches showed potassium channel openings only with micromolar calcium present at the cytoplasmic side; activity increased steeply both with depolarization and with increasing calcium concentration. The single-channel conductance was 126 pS with symmetrical potassium concentrations. The mean open time of the channels was clearly different for channels having different substituent blocks of amino acids. The results suggest that alternative splicing gives rise to a large family of functionally diverse, calcium-activated potassium channels.

摘要

通过注射从果蝇黑腹果蝇slo基因座的互补DNA体外转录的RNA,在非洲爪蟾卵母细胞中表达钙激活钾通道。发现许多cDNA编码约1200个氨基酸的密切相关蛋白质。这些蛋白质的预测序列在假定的细胞内区域中327至797位残基之间的五个已确定位置处通过氨基酸块的取代而不同。切除的内向外膜片仅在细胞质侧存在微摩尔钙时显示钾通道开放;活性随着去极化和钙浓度的增加而急剧增加。在对称钾浓度下,单通道电导为126 pS。具有不同氨基酸取代块的通道的通道平均开放时间明显不同。结果表明,可变剪接产生了一个功能多样的钙激活钾通道大家族。

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