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酮诺司特罗氮丙啶,一种激动性雌激素受体亲和标记物:其生物活性及雌激素受体共价标记的研究

Ketononestrol aziridine, an agonistic estrogen receptor affinity label: study of its bioactivity and estrogen receptor covalent labeling.

作者信息

Elliston J F, Zablocki J A, Katzenellenbogen B S, Katzenellenbogen J A

出版信息

Endocrinology. 1987 Aug;121(2):667-76. doi: 10.1210/endo-121-2-667.

Abstract

Ketononestrol aziridine [(6R,TS)1-(N-aziridinyl)6,7-bis-(4-hydroxyphenyl)5-nonamone (KNA)], an aziridine derivative of hexestrol, is an estrogenic affinity label for the estrogen receptor (ER). It has an apparent relative binding affinity 8% that of estradiol and shows time-dependent irreversible binding to the ER in uterine cytosol preparations and intact human breast cancer cells (MCF-7). The agonistic activity of KNA is evident in MCF-7 cells in culture, where it increases the cell growth rate and elevates the level of progesterone receptor. KNA was prepared in high specific activity tritium-labeled form by iodination of a methanesulfonate precursor, followed by catalytic tritium-iodine exchange and aziridinylation; the material prepared has high radiochemical purity and a specific activity of 67 Ci/mmol. The covalent attachment of [3H]KNA to the ER can be followed directly by a solvent precipitation assay. In cytosol preparations of uterine ER, labeling with [3H]KNA proceeds in a time-, concentration-, and temperature-dependent manner; labeling is efficient and selective and, by competition studies, was shown to be estrogen specific. ER in intact MCF-7 cells can also be covalently labeled by treatment with [3H]KNA. Receptor covalently labeled with [3H]KNA sediments as a 4S species on high salt sucrose gradients, and its sedimentation position is shifted by treatment with monoclonal antireceptor antibodies. On sodium dodecyl sulfate-polyacrylamide gels, the principal labeled species migrates with a mol wt of 66,000. KNA should prove to be a useful probe for studies on receptor structure, function, and chromatin interactions, particularly when the behavior of a receptor-agonist complex is being investigated.

摘要

酮诺雌醇氮丙啶[(6R,TS)1-(N-氮丙啶基)6,7-双-(4-羟基苯基)5-壬酮(KNA)],己烯雌酚的氮丙啶衍生物,是雌激素受体(ER)的一种雌激素亲和标记物。它的表观相对结合亲和力为雌二醇的8%,并在子宫胞质溶胶制剂和完整的人乳腺癌细胞(MCF-7)中显示出与ER的时间依赖性不可逆结合。KNA的激动活性在培养的MCF-7细胞中很明显,它能提高细胞生长速率并提高孕酮受体水平。KNA通过甲磺酸酯前体的碘化制备成高比活度的氚标记形式,随后进行催化氚-碘交换和氮丙啶化;所制备的材料具有高放射化学纯度和67 Ci/mmol的比活度。[3H]KNA与ER的共价结合可以通过溶剂沉淀法直接跟踪。在子宫ER的胞质溶胶制剂中,用[3H]KNA标记以时间、浓度和温度依赖性方式进行;标记是高效且选择性的,通过竞争研究表明是雌激素特异性的。完整的MCF-7细胞中的ER也可以用[3H]KNA处理进行共价标记。用[3H]KNA共价标记的受体在高盐蔗糖梯度上以4S物种沉降,其沉降位置通过用单克隆抗受体抗体处理而发生移动。在十二烷基硫酸钠-聚丙烯酰胺凝胶上,主要的标记物种以66,000的分子量迁移。KNA应该被证明是研究受体结构、功能和染色质相互作用的有用探针,特别是在研究受体-激动剂复合物的行为时。

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