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通过共聚焦显微镜分析雌激素受体与荧光他莫昔芬衍生物FLTX1的共定位

Colocalization of Estrogen Receptors with the Fluorescent Tamoxifen Derivative, FLTX1, Analyzed by Confocal Microscopy.

作者信息

Morales Araceli, Marín Raquel, Marrero-Alonso Jorge, Boto Alicia, Díaz Mario

机构信息

Department of Physiology, Institute of Biomedical Technologies (ITB), Centre for Biomedical Research of the Canary Islands (CIBICAN), University of La Laguna, Tenerife, Spain.

Departamento de Fisiología, Facultad de Medicina, University of La Laguna, Tenerife, Spain.

出版信息

Methods Mol Biol. 2016;1366:163-173. doi: 10.1007/978-1-4939-3127-9_13.

Abstract

Tamoxifen is a selective estrogen receptor modulator that competitively binds the ligand-binding domain of estrogen receptors. Binding of tamoxifen displaces its cognate ligand, 17β-estradiol, thereby hampering the activation of estrogen receptors. Cellular labeling of ER is typically carried out using specific antibodies which require permeabilization of cells, incubation with secondary antibodies, and are expensive and time consuming. In this article, we describe the usefulness of FLTX1, a novel fluorescent tamoxifen derivative, which allows the labeling of estrogen receptors in immunocytochemistry and immunohistochemistry studies, both under permeabilized and non-permeabilized conditions. Further, besides labeling canonical estrogen receptors, this novel fluorescent probe is also suitable for the identification of unconventional targets such membrane estrogen receptors as well as other noncanonical targets, some of which are likely responsible for the number of undesired side effects reported during long-term tamoxifen treatments.

摘要

他莫昔芬是一种选择性雌激素受体调节剂,可竞争性结合雌激素受体的配体结合域。他莫昔芬的结合取代了其同源配体17β-雌二醇,从而阻碍雌激素受体的激活。雌激素受体的细胞标记通常使用特异性抗体进行,这需要使细胞通透、与二抗孵育,且成本高、耗时。在本文中,我们描述了一种新型荧光他莫昔芬衍生物FLTX1的用途,它可在免疫细胞化学和免疫组织化学研究中,在通透和非通透条件下对雌激素受体进行标记。此外,除了标记经典雌激素受体外,这种新型荧光探针还适用于识别非常规靶点,如膜雌激素受体以及其他非经典靶点,其中一些可能是长期他莫昔芬治疗期间报告的许多不良副作用的原因。

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