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依次使用去污剂对膜离子转运蛋白进行增溶和重组。

Sequential use of detergents for solubilization and reconstitution of a membrane ion transporter.

作者信息

Ambesi A, VanAlstyne E L, Bagwell E E, Lindenmayer G E

机构信息

Department of Pharmacology, Medical University of South Carolina, Charleston 29425.

出版信息

Anal Biochem. 1991 Nov 1;198(2):312-7. doi: 10.1016/0003-2697(91)90431-r.

Abstract

Solubilization and reconstitution of the cardiac sarcolemmal Na+/Ca2+ exchanger by use of the anionic detergent cholate and its application for reconstitution of the exchanger following solubilization with zwitterionic or nonionic detergents is described. Solubilization and reconstitution with cholate provided a 32.6-fold enrichment of Na+/Ca2+ exchange activity over sarcolemmal vesicles (5.2 to 170 nmol/mg/s) with 202% recovery of total activity. In combination with asolectin, the cholate dilution technique (H. Miyamoto and E. Racker, J. Biol. Chem. 255, 2656, 1980) offers a rapid and simple means for reconstitution and provides good recovery of total and specific Na+/Ca2+ exchange activity. However, the use of anionic detergents for solubilization precludes the use of certain chromatographic procedures for protein purification. Conversely, nonionic and zwitterionic detergents permit effective use of available chromatographic techniques, but can be troublesome during reconstitution. We have combined the advantages of solubilization with nonionic and zwitterionic detergents with the advantages of reconstitution by cholate dilution. Reconstitution of the exchanger, after solubilization with 3-[(3-cholamidopropyl)-dimethyl-ammonio]-1-propanesulfonate (Chaps) or n-octyl-beta-D-glucoside, was accomplished by the addition of a cholate/asolectin medium followed by dilution. Na+/Ca2+ exchange activity was enriched 30.7-fold with 196% recovery with Chaps and 34.1-fold with 204% recovery with n-octyl-beta-D-glucoside. The presence of Chaps was found to shift the optimal asolectin concentration for reconstitution from 15 mg/ml (cholate alone) to 25 mg/ml. In addition, pelleting of proteoliposomes subsequent to reconstitution resulted in greatest recovery of total activity when volumes were kept below 1.0 ml.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

描述了使用阴离子去污剂胆酸盐对心肌肌膜钠钙交换体进行增溶和重构,以及其在两性离子或非离子去污剂增溶后对该交换体进行重构的应用。用胆酸盐进行增溶和重构使钠钙交换活性比肌膜小泡富集了32.6倍(5.2至170纳摩尔/毫克/秒),总活性回收率达202%。与大豆卵磷脂结合,胆酸盐稀释技术(H. 宫本和E. 拉克尔,《生物化学杂志》255, 2656, 1980)提供了一种快速简便的重构方法,并能很好地回收总钠钙交换活性和特异性钠钙交换活性。然而,使用阴离子去污剂进行增溶排除了使用某些蛋白质纯化色谱方法的可能性。相反,非离子和两性离子去污剂允许有效使用现有的色谱技术,但在重构过程中可能会有麻烦。我们将非离子和两性离子去污剂增溶的优点与胆酸盐稀释重构的优点结合起来。在用3-[(3-胆酰胺丙基)-二甲基-铵基]-1-丙烷磺酸盐(Chaps)或正辛基-β-D-葡萄糖苷增溶后,通过加入胆酸盐/大豆卵磷脂培养基然后稀释来完成交换体的重构。用Chaps时钠钙交换活性富集了30.7倍,回收率为196%,用正辛基-β-D-葡萄糖苷时富集了34.1倍,回收率为204%。发现Chaps的存在使重构的最佳大豆卵磷脂浓度从15毫克/毫升(单独使用胆酸盐时)变为25毫克/毫升。此外,重构后蛋白脂质体沉淀时,当体积保持在1.0毫升以下时,总活性回收率最高。(摘要截短于250字)

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