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CB1受体的特异性检测;大麻素CB1受体抗体并非完全相同!

Specific detection of CB1 receptors; cannabinoid CB1 receptor antibodies are not all created equal!

作者信息

Grimsey Natasha L, Goodfellow Catherine E, Scotter Emma L, Dowie Megan J, Glass Michelle, Graham E Scott

机构信息

Department of Pharmacology and Clinical Pharmacology, University of Auckland, Private Bag 92019, Auckland, New Zealand.

出版信息

J Neurosci Methods. 2008 Jun 15;171(1):78-86. doi: 10.1016/j.jneumeth.2008.02.014. Epub 2008 Mar 2.

DOI:10.1016/j.jneumeth.2008.02.014
PMID:18406468
Abstract

The study of endogenous cannabinoid CB1 receptor proteins in neuronal tissues and cells relies on the availability of highly specific antibodies. We have tested the ability of a series of CB1 antibodies to detect endogenous receptors in brain as well as hemagglutinin (HA)-tagged receptors transfected into HEK-293 cells using a combination of immunological methods. An initial comparison of several CB1 antibodies in mouse brain revealed substantial differences in staining pattern to ligand binding by autoradiography. Antibodies were then tested immunocytochemically against HEK cells expressing HA-tagged rat and human CB1 receptors. None of the commercial antibodies tested were able to detect the receptor in this context. All antibodies were then screened by Western blotting using lysates from the HEK cells and rodent brain homogenates. Again, none of the commercially available antibodies detected proteins of the correct molecular weight in transfected cell lines or brain homogenates, although all recognized multiple proteins in brain tissues. We conclude that the commercially available antibodies we tested failed to detect CB1 receptors abundantly expressed in HEK cells or native receptors in brain slices or homogenates. As such, comprehensive validation of the specificity of these CB1 antibodies for a particular application is essential before use.

摘要

对神经组织和细胞中内源性大麻素CB1受体蛋白的研究依赖于高特异性抗体的可用性。我们使用多种免疫学方法,测试了一系列CB1抗体检测大脑中内源性受体以及转染到HEK-293细胞中的血凝素(HA)标记受体的能力。对几种CB1抗体在小鼠大脑中的初步比较显示,通过放射自显影法观察,它们在与配体结合的染色模式上存在显著差异。然后针对表达HA标记的大鼠和人类CB1受体的HEK细胞进行免疫细胞化学测试。在此情况下,所测试的商业抗体均无法检测到该受体。接着使用HEK细胞裂解物和啮齿动物脑匀浆通过蛋白质印迹法对所有抗体进行筛选。同样,尽管所有商业抗体都能识别脑组织中的多种蛋白质,但在转染细胞系或脑匀浆中,没有一种商业抗体能检测到正确分子量的蛋白质。我们得出结论,我们测试的商业抗体无法检测到在HEK细胞中大量表达的CB1受体或脑切片或匀浆中的天然受体。因此,在使用前对这些CB1抗体针对特定应用的特异性进行全面验证至关重要。

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