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N-(对叠氮基-3-[¹²⁵I]碘苯乙基)螺哌隆与人神经母细胞瘤细胞中的P-糖蛋白及另一种多药结合蛋白——螺哌嗜素的特定区域结合。

N-(p-azido-3-[125I]iodophenethyl)spiperone binds to specific regions of P-glycoprotein and another multidrug binding protein, spiperophilin, in human neuroblastoma cells.

作者信息

Safa A R, Agresti M, Bryk D, Tamai I

机构信息

Department of Medicine, University of Chicago, Illinois 60637-1470.

出版信息

Biochemistry. 1994 Jan 11;33(1):256-65. doi: 10.1021/bi00167a034.

Abstract

P-glycoprotein (P-gp) is an energy-dependent drug extrusion pump with broad specificity for diverse hydrophobic anticancer agents and compounds known to reverse multidrug resistance (MDR). Among MDR reversing agents, phenothiazines (PTZs) and related compounds may sensitize MDR by interacting with a specific binding site(s) on P-gp and by other mechanisms. In order (1) to identify a binding site for PTZs and related compounds on P-gp, (2) to examine whether these compounds and other MDR modulators bind to the same domains of P-gp, and (3) to identify proteins with high specificity for these neuroleptic agents and other MDR modulators, we used a butyrophenone D2-dopamine receptor photoaffinity probe, N-(p-azido-3-[125I]iodophenethyl)spiperone ([125I]NAPS). [125I]NAPS was actively effluxed from vincristine (VCR)-resistant SH-SY5Y/VCR human neuroblastoma cells, and nonradioactive I-NAPS was a potent chemosensitizing agent. After photolabeling, the probe bound specifically and with high efficiency to P-gp and to another multidrug binding 17-kDa membrane-bound protein, spiperophilin, in these cells. The efficiency of [125I]NAPS binding to P-gp was 5-6-fold more than [3H]azidopine and [125I]arylazidoprazosin ([125I]AAP), known photoaffinity analogs for P-gp. [125I]NAPS photolabeling of P-gp was preferentially competed by MDR-related drugs, with vinblastine > VCR > colchicine > doxorubicin > actinomycin D. Many drugs that are known to reverse MDR were potent inhibitors of [125I]NAPS binding to P-gp. While PTZs and related compounds were potent inhibitors of [125I]NAPS binding to P-gp, most of them enhanced the binding of [125I]AAP significantly. cis-Flupentixol increased the binding of [125I]AAP to P-gp 9-fold more than did trans-flupentixol, but both were potent inhibitors of [125I]NAPS binding, suggesting their stereoselective effect on the [125I]AAP binding site. Proteolysis of [125I]NAPS-bound P-gp with Staphylococcus aureus V8 protease revealed that this probe binds to two major peptides, 6 and 8 kDa, and a number of minor ones, while [125I]AAP binds to only an 8-kDa peptide. These results suggest that modulators of MDR may interact with separate or overlapping domains. Furthermore, most MDR modulators, dopaminergic drugs, and beta-adrenergic antagonists used also inhibited binding of [125I]-NAPS to spiperophilin, suggesting that this protein may be a target for these drugs.

摘要

P-糖蛋白(P-gp)是一种能量依赖性药物外排泵,对多种疏水性抗癌药物和已知可逆转多药耐药性(MDR)的化合物具有广泛的特异性。在MDR逆转剂中,吩噻嗪类(PTZs)及相关化合物可通过与P-gp上的特定结合位点相互作用以及其他机制使MDR致敏。为了(1)确定PTZs及相关化合物在P-gp上的结合位点,(2)研究这些化合物和其他MDR调节剂是否结合到P-gp的相同结构域,以及(3)鉴定对这些抗精神病药物和其他MDR调节剂具有高特异性的蛋白质,我们使用了一种丁酰苯D2-多巴胺受体光亲和探针,N-(对叠氮基-3-[125I]碘苯乙基)螺哌隆([125I]NAPS)。[125I]NAPS从长春新碱(VCR)耐药的SH-SY5Y/VCR人神经母细胞瘤细胞中被主动外排,且非放射性的I-NAPS是一种有效的化学增敏剂。光标记后,该探针在这些细胞中特异性且高效地结合到P-gp以及另一种多药结合的17 kDa膜结合蛋白,螺哌隆亲和蛋白上。[125I]NAPS与P-gp的结合效率比已知的P-gp光亲和类似物[3H]叠氮平及[125I]芳基叠氮哌唑嗪([125I]AAP)高5至6倍。P-gp的[125I]NAPS光标记优先被MDR相关药物竞争,其竞争能力顺序为长春碱>VCR>秋水仙碱>阿霉素>放线菌素D。许多已知可逆转MDR的药物是[125I]NAPS与P-gp结合的有效抑制剂。虽然PTZs及相关化合物是[125I]NAPS与P-gp结合的有效抑制剂,但它们中的大多数显著增强了[125I]AAP的结合。顺式氟哌噻吨使[125I]AAP与P-gp的结合比反式氟哌噻吨增加9倍,但两者都是[125I]NAPS结合的有效抑制剂,表明它们对[125I]AAP结合位点具有立体选择性作用。用金黄色葡萄球菌V8蛋白酶对[125I]NAPS结合的P-gp进行蛋白水解显示,该探针结合到两条主要肽段,6 kDa和8 kDa,以及一些较小的肽段,而[125I]AAP仅结合到一条8 kDa的肽段。这些结果表明MDR调节剂可能与不同或重叠的结构域相互作用。此外,所使用的大多数MDR调节剂、多巴胺能药物和β-肾上腺素能拮抗剂也抑制[125I]-NAPS与螺哌隆亲和蛋白的结合,表明该蛋白可能是这些药物的作用靶点。

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