• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.1210/endo-121-2-667
PMID:3595536
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。

相似文献

1
Ketononestrol aziridine, an agonistic estrogen receptor affinity label: study of its bioactivity and estrogen receptor covalent labeling.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
Endocrinology. 1987 Aug;121(2):667-76. doi: 10.1210/endo-121-2-667.
2
Identification of cysteine 530 as the covalent attachment site of an affinity-labeling estrogen (ketononestrol aziridine) and antiestrogen (tamoxifen aziridine) in the human estrogen receptor.确定半胱氨酸530为人雌激素受体中亲和标记雌激素(酮炔诺醇氮丙啶)和抗雌激素(他莫昔芬氮丙啶)的共价连接位点。
J Biol Chem. 1989 Oct 15;264(29):17476-85.
3
Comparative analysis of estrogen receptors covalently labeled with an estrogen and an antiestrogen in several estrogen target cells as studied by limited proteolysis.
J Steroid Biochem. 1988 Jun;29(6):559-69. doi: 10.1016/0022-4731(88)90152-5.
4
Estrogenic affinity labels: synthesis, irreversible receptor binding, and bioactivity of aziridine-substituted hexestrol derivatives.
J Med Chem. 1987 May;30(5):829-38. doi: 10.1021/jm00388a015.
5
Characterization of the estrogen receptor and its dynamics in MCF-7 human breast cancer cells using a covalently attaching antiestrogen.使用共价连接的抗雌激素对MCF-7人乳腺癌细胞中的雌激素受体及其动力学进行表征。
Endocrinology. 1984 Jul;115(1):143-53. doi: 10.1210/endo-115-1-143.
6
Desmethylnafoxidine aziridine: an electrophilic affinity label for the estrogen receptor with high efficiency and selectivity.
J Steroid Biochem. 1987 Sep;28(3):233-45. doi: 10.1016/0022-4731(87)91014-4.
7
Dynamics of estrogen receptor turnover in uterine cells in vitro and in uteri in vivo.体外子宫细胞和体内子宫中雌激素受体周转的动力学
Endocrinology. 1986 Nov;119(5):2038-46. doi: 10.1210/endo-119-5-2038.
8
Antiestrogen binding in antiestrogen growth-resistant estrogen-responsive clonal variants of MCF-7 human breast cancer cells.抗雌激素在MCF-7人乳腺癌细胞的抗雌激素生长抗性雌激素反应性克隆变体中的结合。
Cancer Res. 1984 Nov;44(11):5038-45.
9
Selection and characterization of a breast cancer cell line resistant to the antiestrogen LY 117018.一种抗雌激素LY 117018的乳腺癌细胞系的筛选与鉴定
Endocrinology. 1985 Oct;117(4):1409-17. doi: 10.1210/endo-117-4-1409.
10
Unique molecular properties of a urea- and salt-stable DNA-binding estrogen receptor dimer covalently labeled with the antiestrogen [3H]desmethylnafoxidine aziridine. A comparison with the estrogen-receptor complex.用抗雌激素[3H]去甲基萘福昔定氮丙啶共价标记的尿素和盐稳定的DNA结合雌激素受体二聚体的独特分子特性。与雌激素受体复合物的比较。
Mol Endocrinol. 1990 Feb;4(2):255-67. doi: 10.1210/mend-4-2-255.