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从纹状体膜中溶解和重组D-1多巴胺受体所需的特定磷脂

Specific phospholipid requirements for the solubilization and reconstitution of D-1 dopamine receptors from striatal membranes.

作者信息

Balen P, Kimura K, Sidhu A

机构信息

Department of Pediatrics, Georgetown University Children's Medical Center, Georgetown University, Washington, D.C. 20007.

出版信息

Biochemistry. 1994 Feb 15;33(6):1539-44. doi: 10.1021/bi00172a034.

Abstract

We have reported the solubilization and reconstitution of functional D-1 dopamine receptors from rat striatal tissue, using sodium cholate as detergent [Sidhu, A. (1988) Biochemistry 27, 8768-8776]. Critical to our method of extraction was the absolute requirement for the persistent presence of a crude extract of phospholipids (PLs) from bovine brain, during both solubilization of membranes and reconstitution of the soluble extract into PL vesicles. In the absence of PLs, fewer than 10% of the receptors were recovered, while in the presence of PLs, 40% of the receptors were reconstituted into vesicles. To probe the composition of PLs required by D-1 dopamine receptors during these extraction procedures, specific PLs of a defined composition were used during either solubilization or reconstitution alone or during both solubilization and reconstitution. Phosphatidylcholine (PC), when used during the solubilization procedure alone or during both solubilization and reconstitution, resulted in recovery of 41-48% of the D-1 dopamine receptors but was 3.7-fold less effective when present during reconstitution alone (11%). Phosphatidylethanolamine (PE), when used during reconstitution alone, resulted in recovery of nearly 25% of the D-1 dopamine receptors. When PE was present during either solubilization or both solubilization and reconstitution, 6-11% of the receptors were recovered. If PE was used with PC in ratios of 1:1 or 2:1, respectively, 28-38% of the receptors were recovered. When PL vesicles of PE:PC were present in ratios of 1:2 during both solubilization and reconstitution, the maximum theoretical (74-87%) recovery of total receptor binding sites was achieved.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们曾报道过,利用胆酸钠作为去污剂,从大鼠纹状体组织中增溶并重构功能性D-1多巴胺受体[西杜,A.(1988年)《生物化学》27卷,8768 - 8776页]。我们的提取方法的关键在于,在膜增溶以及将可溶性提取物重构到磷脂(PL)囊泡的过程中,绝对需要持续存在牛脑粗制磷脂提取物。在没有磷脂的情况下,回收的受体不到10%,而在有磷脂的情况下,40%的受体被重构到囊泡中。为了探究在这些提取过程中D-1多巴胺受体所需磷脂的组成,在单独的增溶或重构过程中,或在增溶和重构过程中都使用了特定组成的磷脂。单独在增溶过程中或在增溶和重构过程中都使用磷脂酰胆碱(PC)时,可回收41 - 48%的D-1多巴胺受体,但仅在重构过程中存在时效果要低3.7倍(11%)。单独在重构过程中使用磷脂酰乙醇胺(PE)时,可回收近25%的D-1多巴胺受体。当PE存在于增溶过程中或增溶和重构过程中时,回收的受体为6 - 11%。如果将PE与PC分别以1:1或2:1的比例使用,可回收28 - 38%的受体。当在增溶和重构过程中,PE:PC的磷脂囊泡以1:2的比例存在时,实现了总受体结合位点的最大理论回收率(74 - 87%)。(摘要截选至250字)

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