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Single chloride-selective channel from cardiac sarcoplasmic reticulum studied in planar lipid bilayers.

作者信息

Rousseau E

机构信息

Department of Biochemistry and Nutrition, University of North Carolina, Chapel Hill 27599.

出版信息

J Membr Biol. 1989 Aug;110(1):39-47. doi: 10.1007/BF01870991.

DOI:10.1007/BF01870991
PMID:2477549
Abstract

The behavior of single Cl- channel was studied by fusing isolated canine cardiac sarcoplasmic reticulum (SR) vesicles into planar lipid bilayers. The channel exhibited unitary conductance of 55 pS (in 260 mM Cl-) and steady-state activation. Subconductance states were observed. Open probability was dependent on holding potentials (-60 to +60 mV) and displayed a bell-shaped relationship, with probability values ranging from 0.2 to 0.8 with a maximum at -10 mV. Channel activity was irreversibly inhibited by DIDS, a stilbene derivative. Time analysis revealed the presence of one time constant for the full open state and three time constants for the closed states. The open and the longer closed time constants were found to be voltage dependent. The behavior of the channel was not affected by changing Ca2+ and Mg2+ concentrations in both chambers, nor by adding millimolar adenosine triphosphate, or by changing the pH from 7.4 to 6.8. The presence of sulfate anions decreased the unit current amplitude, but did not affect the open probability. These results reveal that at the unitary level the cardiac SR anion-selective channel has distinctive as well as similar electrical properties characteristic of other types of Cl- channels.

摘要

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本文引用的文献

1
Kinetic analysis of the inhibition of anion transport in sarcoplasmic reticulum vesicles by a disulfonic stilbene derivative. Measurement of the change in chloride-diffusion potential by using a fluorescent cyanine dye.二磺酸芪衍生物对肌浆网囊泡中阴离子转运抑制作用的动力学分析。使用荧光花青染料测量氯离子扩散电位的变化。
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他莫昔芬对心肌肌浆网氯通道的抑制作用。
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A large-conductance anion channel of the Golgi complex.高尔基体复合体的一种大电导阴离子通道。
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GOLAC: an endogenous anion channel of the Golgi complex.GOLAC:高尔基体复合物的一种内源性阴离子通道。
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10
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J Membr Biol. 1995 Sep;147(1):7-22. doi: 10.1007/BF00235394.
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