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由重组到脂质体中并吸附在黑色脂质膜上的龙虾肌肉部分纯化的钠/钙交换器产生的电流:钙离子光解激活。

Electrical currents generated by a partially purified Na/Ca exchanger from lobster muscle reconstituted into liposomes and adsorbed on black lipid membranes: activation by photolysis of Ca2+.

作者信息

Eisenrauch A, Juhaszova M, Ellis-Davies G C, Kaplan J H, Bamberg E, Blaustein M P

机构信息

Laboratory of Biophysical Chemistry, Max-Planck-Institute für Biophysik, Frankfurt/M, Germany.

出版信息

J Membr Biol. 1995 May;145(2):151-64. doi: 10.1007/BF00237373.

Abstract

The Na/Ca exchanger from lobster muscle crossreacts specifically with antibodies raised against the dog heart Na/Ca exchanger. Immunoblots of the lobster muscle and mammalian heart exchangers, following SDS-PAGE, indicate that the invertebrate and mammalian exchangers have similar molecular weights: about 120 kDa. The exchanger from lobster muscle was partially purified and functionally reconstituted into asolectin vesicles which were loaded with 160 mM NaCl. 45Ca uptake by these proteoliposomes was promoted by replacing 160 mM NaCl in the external medium with 160 mM KCl to produce an outwardly-directed Na+ concentration gradient. When the proteoliposomes were adsorbed onto black lipid membranes (BLM), and DM-Nitrophen-Ca2+ ("caged Ca2+") was added to the KCl medium, photolytically-evoked Ca2+ concentration jumps elicited transient electric currents. These currents corresponded to positive charge exiting from the proteoliposomes, and were consistent with the Na/Ca exchanger-mediated exit of 3 Na+ in exchange for 1 entering Ca2+. The current was dependent upon the Ca2+ concentration jump, the protein integrity, and the outwardly directed Na+ gradient. KCl-loaded proteoliposomes did not produce any current. Low external Na+ concentrations augmented the current, whereas Na+ concentrations > 25 mM reduced the current. The dependence of the current on free Ca2+ was Michaelis-Menten-like, with half-maximal activation (KM(Ca)) at < 10 microM Ca2+. Caged Sr2+ and Ba2+, but not Mg2+, also supported photolysis-evoked outward current, as did Ni2+, but not Mn2+. However, Mg2+ and Mn2+ augmented the Ca-dependent current, perhaps by facilitating the adsorption of proteoliposomes to the BLM. The Ca-dependent current was irreversibly blocked by La3+ (added as 200 microM DMN-La3+). The results indicate that the properties of the Na/Ca exchanger can be studied with these electro-physiological methods.

摘要

龙虾肌肉中的钠钙交换蛋白与针对犬心脏钠钙交换蛋白产生的抗体发生特异性交叉反应。十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)后对龙虾肌肉和哺乳动物心脏交换蛋白进行免疫印迹分析,结果表明,无脊椎动物和哺乳动物的交换蛋白具有相似的分子量:约120 kDa。从龙虾肌肉中部分纯化出交换蛋白,并将其功能重组到装载有160 mM氯化钠的大豆卵磷脂囊泡中。通过用160 mM氯化钾替代外部介质中的160 mM氯化钠以产生外向型钠离子浓度梯度,可促进这些蛋白脂质体对45钙的摄取。当蛋白脂质体吸附到黑色脂质膜(BLM)上,并向氯化钾介质中加入二甲基硝基苯酚-钙(“笼锁钙”)时,光解引发的钙离子浓度跃变会引发瞬态电流。这些电流对应于从蛋白脂质体流出的正电荷,并且与钠钙交换蛋白介导的3个钠离子流出以交换1个进入的钙离子一致。电流取决于钙离子浓度跃变、蛋白质完整性以及外向型钠离子梯度。装载氯化钾的蛋白脂质体不产生任何电流。低外部钠离子浓度会增强电流,而钠离子浓度>25 mM时会降低电流。电流对游离钙离子的依赖性呈米氏(Michaelis-Menten)样,在钙离子浓度<10 microM时达到半数最大激活(KM(Ca))。笼锁锶离子和钡离子(而非镁离子)也支持光解引发的外向电流,镍离子也支持,但锰离子不支持。然而,镁离子和锰离子会增强钙离子依赖性电流,可能是通过促进蛋白脂质体吸附到黑色脂质膜上实现的。钙离子依赖性电流被镧离子(以200 microM二甲基硝基苯酚-镧离子形式添加)不可逆地阻断。结果表明,可以用这些电生理方法研究钠钙交换蛋白的特性。

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