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本文引用的文献

1
Thimerosal interacts with the Ca2+ release channel ryanodine receptor from skeletal muscle sarcoplasmic reticulum.硫柳汞与骨骼肌肌浆网中的钙离子释放通道兰尼碱受体相互作用。
J Biol Chem. 1995 Dec 15;270(50):29644-7. doi: 10.1074/jbc.270.50.29644.
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The effects of thimerosal on calcium uptake and inositol 1,4,5-trisphosphate-induced calcium release in cerebellar microsomes.硫柳汞对小脑微粒体钙摄取及肌醇1,4,5-三磷酸诱导的钙释放的影响。
Biochem J. 1993 Feb 1;289 ( Pt 3)(Pt 3):883-7. doi: 10.1042/bj2890883.
3
Sulfhydryl reagents and cAMP-dependent kinase increase the sensitivity of the inositol 1,4,5-trisphosphate receptor in hepatocytes.巯基试剂和环磷酸腺苷依赖性激酶可提高肝细胞中肌醇1,4,5-三磷酸受体的敏感性。
J Biol Chem. 1993 Aug 25;268(24):17917-23.
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Thiol reagents increase the affinity of the inositol 1,4,5-trisphosphate receptor.硫醇试剂可增加肌醇1,4,5-三磷酸受体的亲和力。
J Biol Chem. 1993 Aug 5;268(22):16488-94.
5
Redundant mechanisms of calcium-induced calcium release underlying calcium waves during fertilization of sea urchin eggs.海胆卵受精过程中钙波产生时钙诱导钙释放的冗余机制。
Science. 1993 Jul 16;261(5119):348-52. doi: 10.1126/science.8392748.
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Nature. 1993 Jan 28;361(6410):315-25. doi: 10.1038/361315a0.
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The high affinity state of inositol 1,4,5-trisphosphate receptor is a functional state.肌醇1,4,5-三磷酸受体的高亲和力状态是一种功能状态。
J Biol Chem. 1993 Nov 15;268(32):24078-82.
8
Two calcium-binding sites mediate the interconversion of liver inositol 1,4,5-trisphosphate receptors between three conformational states.两个钙结合位点介导肝脏肌醇1,4,5-三磷酸受体在三种构象状态之间的相互转化。
Biochem J. 1994 Jul 15;301 ( Pt 2)(Pt 2):591-8. doi: 10.1042/bj3010591.
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Purified reconstituted inositol 1,4,5-trisphosphate receptors. Thiol reagents act directly on receptor protein.
J Biol Chem. 1994 Nov 18;269(46):28972-8.
10
ATP modulates the function of inositol 1,4,5-trisphosphate-gated channels at two sites.三磷酸腺苷(ATP)在两个位点调节肌醇1,4,5-三磷酸门控通道的功能。
Neuron. 1993 Jun;10(6):1175-84. doi: 10.1016/0896-6273(93)90065-y.

肌醇1,4,5-三磷酸门控钙离子通道:蛋白质硫醇试剂硫柳汞对通道活性的影响。

The inositol 1,4,5-trisphosphate-gated Ca2+ channel: effect of the protein thiol reagent thimerosal on channel activity.

作者信息

Thrower E C, Duclohier H, Lea E J, Molle G, Dawson A P

机构信息

School of Biological Sciences, University of East Anglia, Norwich, U.K.

出版信息

Biochem J. 1996 Aug 15;318 ( Pt 1)(Pt 1):61-6. doi: 10.1042/bj3180061.

DOI:10.1042/bj3180061
PMID:8761453
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1217589/
Abstract

The solubilized partially purified Ins(1,4,5)P3-sensitive Ca2+ channel from rat cerebellum has been reconstituted into planar lipid bilayer membranes by the 'tip-dip' method [Ehrlich (1992) Methods Enzymol. 207, 463-471] allowing low noise current records. Single-channel events have been recorded. In the presence of 10 microM Ins(1,4,5)P3, 50 microM ATP, and 0.2 microM Ca2+ the Ins(1,4,5)P3 receptor channel opens to a conductance level of 53 pS. In the presence of 100 microM thimerosal (TMS), a sulphydryl-oxidizing agent, three subconductance levels (60 pS, 80 pS and 120 pS) were observed. More than one population of mean open times was found, both in the absence and presence of TMS, although TMS affected the length of the open time by decreasing the short opening significantly from 4.05 ms to 2.78 ms and increasing the longer open time from 27.8 ms to 94.8 ms. The results indicate that TMS enhances Ins(1,4,5)P3-induced Ca2+ release by both altering the open times of the channel significantly and causing a shift to higher subconductance levels.

摘要

通过“尖端浸渍”法[埃利希(1992年),《酶学方法》第207卷,第463 - 471页],已将从大鼠小脑中溶解并部分纯化的对肌醇 - 1,4,5 - 三磷酸(Ins(1,4,5)P3)敏感的钙离子通道重组到平面脂质双分子层膜中,从而实现低噪声电流记录。已记录到单通道事件。在存在10微摩尔Ins(1,4,5)P3、50微摩尔三磷酸腺苷(ATP)和0.2微摩尔钙离子的情况下,Ins(1,4,5)P3受体通道开放至53皮西门子的电导水平。在存在100微摩尔硫柳汞(TMS)(一种巯基氧化剂)的情况下,观察到三个亚电导水平(60皮西门子、80皮西门子和120皮西门子)。在不存在和存在TMS的情况下均发现不止一种平均开放时间群体,尽管TMS通过将短开放时间从4.05毫秒显著降低至2.78毫秒,并将长开放时间从27.8毫秒增加至94.8毫秒,从而影响了开放时间的长度。结果表明,TMS通过显著改变通道的开放时间并导致向更高亚电导水平的转变,增强了Ins(1,4,5)P3诱导的钙离子释放。