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使用量子点技术对固定组织中的磷酸化蛋白进行定量原位检测。

Quantitative in situ detection of phosphoproteins in fixed tissues using quantum dot technology.

作者信息

Bodo Juraj, Durkin Lisa, Hsi Eric D

机构信息

Department of Clinical Pathology, L-11 Cleveland Clinic, Cleveland, Ohio 44195, USA.

出版信息

J Histochem Cytochem. 2009 Jul;57(7):701-8. doi: 10.1369/jhc.2009.953547. Epub 2009 Mar 30.

Abstract

Detection and quantitation of phosphoproteins (PPs) in fixed tissues will become increasingly important as additional inhibitors of protein kinases enter clinical use and new disease entities are defined by molecular changes affecting PP levels. We characterize fixation conditions suitable for accurate PP quantitation that are achievable in a clinical laboratory and illustrate the utility of in situ quantitation of PPs by quantum dot (QD) nanocrystals in two models: (1) a therapeutic model demonstrating effects of a targeted therapeutic (quantitative reduction of phospho-GSK3beta) in xenografts treated with enzastaurin; and (2) a diagnostic model that identifies elevated levels of nuclear phospho-STAT5 in routine bone marrow biopsies from patients with acute myeloid leukemia based on the presence of the activating FLT3-ITD mutation. Finally, we document production of a well-characterized tissue microarray of widely available cell lines as a multilevel calibrator for validating numerous phosphoprotein assays. QD immunofluorescence is an ideal method for in situ quantitation of PPs in fixed samples, providing valuable cell type-specific and subcellular information about pathway activation in primary tissues.

摘要

随着越来越多的蛋白激酶抑制剂进入临床应用,以及新的疾病实体由影响磷蛋白(PP)水平的分子变化所定义,在固定组织中检测和定量磷蛋白将变得越来越重要。我们描述了在临床实验室中可实现的适合准确PP定量的固定条件,并通过量子点(QD)纳米晶体在两种模型中说明了PP原位定量的实用性:(1)一种治疗模型,展示了在恩杂他滨治疗的异种移植中靶向治疗(磷酸化GSK3β的定量减少)的效果;(2)一种诊断模型,基于激活的FLT3-ITD突变的存在,在急性髓系白血病患者的常规骨髓活检中识别核磷酸化STAT5水平升高。最后,我们记录了一种广泛可用细胞系的特征明确的组织微阵列的制作,作为用于验证众多磷蛋白检测的多级校准物。量子点免疫荧光是固定样品中PP原位定量的理想方法,可提供有关原代组织中途径激活的有价值的细胞类型特异性和亚细胞信息。

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