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通过肽图谱鉴定多巴胺转运体上的光亲和标记配体结合结构域。

Photoaffinity-labeled ligand binding domains on dopamine transporters identified by peptide mapping.

作者信息

Vaughan R A

机构信息

Neuroscience Branch, National Institute on Drug Abuse Addiction Research Center, Baltimore, Maryland 21224, USA.

出版信息

Mol Pharmacol. 1995 May;47(5):956-64.

PMID:7746282
Abstract

Binding domains on rat dopamine transporters for cocaine and 1-(2-diphenylmethoxy)ethyl-4-(3-phenylpropyl)piperazine compounds were identified using controlled proteolysis of photoaffinity-labeled protein and epitope-specific immunoprecipitation of the labeled fragments. Rat dopamine transporters were photoaffinity labeled with 1-[2-(diphenylmethoxy)ethyl]-4-[2-(4-azido- 3-[125I]iodophenyl)ethyl]piperazine ([125I]DEEP) [a 1-(2-di- phenylmethoxy)ethyl-4-(3-phenylpropyl)piperazine analog] or 3 beta-(p-chlorophenyl)tropane-2 beta-carboxylic acid, 4'-azido-3'- [125I]iodophenylethyl ester ([125I]RTI 82) (a cocaine analog) and were gel purified to remove contaminating radioactivity. The resulting samples were treated with V8 protease or trypsin and analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The peptide maps generated with each enzyme were different for each of the ligands, suggesting that the ligands were incorporated into different regions of the protein. Identical peptide maps were generated from striatum- and nucleus accumbens-derived transporters, indicating that these polypeptides are highly similar in primary sequence. The proteolytic fragments generated by V8 protease were localized to specific domains of the protein using antipeptide antibodies corresponding to five different regions of the transporter. Fragments of 10 and 7 kDa from [125I]DEEP-labeled transporters were specifically immunoprecipitated with an antibody generated against amino acids 42-59 (near the first putative trans-membrane domain), whereas a 34-kDa fragment from [125I]RTI 82-labeled transporters was precipitated with three different sera corresponding to regions in the carboxyl-terminal two thirds of the protein. None of the V8 fragments smaller than 45 kDa, containing either photolabel, was altered in molecular mass by N-deglycosylation. The results indicate that photoincorporation of [125I]DEEP occurs in the amino half of the dopamine transporter, near the first two transmembrane helices, whereas [125I]RTI 82 labels the carboxyl-terminal region of the protein, between transmembrane domains 4 and 12.

摘要

通过对光亲和标记蛋白进行可控蛋白酶解以及对标记片段进行表位特异性免疫沉淀,确定了大鼠多巴胺转运体上可卡因和1-(2-二苯基甲氧基)乙基-4-(3-苯基丙基)哌嗪化合物的结合结构域。大鼠多巴胺转运体用1-[2-(二苯基甲氧基)乙基]-4-[2-(4-叠氮基-3-[125I]碘苯基)乙基]哌嗪([125I]DEEP)[一种1-(2-二苯基甲氧基)乙基-4-(3-苯基丙基)哌嗪类似物]或3β-(对氯苯基)托烷-2β-羧酸4'-叠氮基-3'-[125I]碘苯乙酯([125I]RTI 82)(一种可卡因类似物)进行光亲和标记,然后进行凝胶纯化以去除污染性放射性。将所得样品用V8蛋白酶或胰蛋白酶处理,并通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳进行分析。每种配体用每种酶生成的肽图都不同,这表明配体被掺入到蛋白质的不同区域。从纹状体和伏隔核来源的转运体生成了相同的肽图,表明这些多肽的一级序列高度相似。使用对应于转运体五个不同区域的抗肽抗体,将V8蛋白酶产生的蛋白水解片段定位到蛋白质的特定结构域。来自[125I]DEEP标记转运体的10 kDa和7 kDa片段用针对氨基酸42-59(靠近第一个假定跨膜结构域)产生的抗体进行特异性免疫沉淀,而来自[125I]RTI 82标记转运体的34 kDa片段用对应于蛋白质羧基末端三分之二区域的三种不同血清进行沉淀。小于45 kDa的含有任何一种光标记的V8片段,其分子量都不会因N-去糖基化而改变。结果表明,[125I]DEEP的光掺入发生在多巴胺转运体的氨基端一半,靠近前两个跨膜螺旋,而[125I]RTI 82标记蛋白质的羧基末端区域,在跨膜结构域4和12之间。

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