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首页> 外文期刊>Pediatric cardiology >Stoichiometry of the slow I ks potassium channel in human embryonic stem cell-derived myocytes
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Stoichiometry of the slow I ks potassium channel in human embryonic stem cell-derived myocytes

机译:人胚胎干细胞来源的心肌细胞中慢Iks钾通道的化学计量

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摘要

The delayed rectifier Iks potassium channel is composed of α-(KCNQ1) and β-(KCNE1) subunits. The stoichiometry of I ks channels is a matter of some debate. Recently some investigators proposed that the number of KCNE1 subunits per KCNQ1 tetramer could be vary from one to four depending on the relative expression of these two genes. Here we review our previous study of biophysical properties of I ks in human embryonic stem cell-derived cardiomyocytes (hESC-CMs) showed that I ks in hESC-CMs is a coassembly channel with a stoichiometry other than 1:1, which could be further modulated by additional KCNE1.
机译:延迟整流器Iks钾离子通道由α-(KCNQ1)和β-(KCNE1)亚基组成。 I ks通道的化学计量是一个有争议的问题。最近,一些研究者提出,根据这两个基因的相对表达,每个KCNQ1四聚体的KCNE1亚基数量可以从一到四个变化。在这里,我们回顾我们以前在人类胚胎干细胞源性心肌细胞(hESC-CMs)中Iks的生物物理特性研究,结果表明hESC-CMs中的Iks是化学计量比为1:1的复合通道,这可能是进一步的由附加的KCNE1调制。

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