A Miniaturized Ligand Binding Assay for EGFR.

International journal of proteomics Pub Date : 2012-01-01 Epub Date: 2012-04-08 DOI:10.1155/2012/247059
Jochen M Schwenk, Oliver Poetz, Robert Zeillinger, Thomas O Joos
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Abstract

In order to study receptor abundance and its function in solutions or in homogenates from clinical specimen, methods such as sandwich or radioimmunoassays are most commonly employed. For the determination of epidermal growth factor receptor (EGFR), we describe the development of a miniaturized bead-based ligand binding assay using its ligand EGF as immobilized capture reagent. This assay was used to analyze lysates from cell lines, and the ligand-bound EGFR was detected using an EGFR-specific antibody combined with a fluorescence-based reporter system. In a proof-of concept study with lysates from breast biopsies, the assay allowed to classify breast cancer samples in accordance to clinically the relevant EGFR cut-off level. The study suggests that such a ligand binding receptor assay could become an integral part of protein profiling procedures to provide additional information about receptor functionality in addition to its abundance.

Abstract Image

Abstract Image

表皮生长因子受体的微型配体结合测定。
为了研究溶液或临床标本匀浆中受体的丰度及其功能,最常用的方法是夹心法或放射免疫法。为了测定表皮生长因子受体(EGFR),我们介绍了一种基于微珠的配体结合测定方法,该方法使用其配体 EGF 作为固定捕获试剂。这种检测方法用于分析细胞系的裂解物,配体结合的表皮生长因子受体通过表皮生长因子受体特异性抗体结合荧光报告系统进行检测。在对乳腺活检组织裂解物进行的概念验证研究中,该检测方法可根据临床上相关的表皮生长因子受体临界水平对乳腺癌样本进行分类。这项研究表明,这种配体结合受体测定法可以成为蛋白质分析程序的一个组成部分,除了提供受体丰度外,还能提供有关受体功能的更多信息。
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