基于单克隆抗体的夹心ELISA检测糖尿病相关自身抗原谷氨酸脱羧酶GAD65。

M Schlosser, J Hahmann, B Ziegler, P Augstein, M Ziegler
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引用次数: 18

摘要

虽然已知有多种检测谷氨酸脱羧酶(GAD65- aab)自身抗体的方法,但尚无GAD65作为自身抗原的敏感定量方法。我们描述了一种基于不同表位特异性的GAD65单克隆抗体(Mc-GAD65-Ab)的夹心ELISA,用于定量胰岛和不同器官/细胞提取物以及从脑提取物制备GAD过程中的GAD65。GAD65通过固相包被的Mc-GAD65-Ab捕获,并通过识别分子nh2末端表位的第二生物素标记的Mc-GAD65-Ab检测。用碱性磷酸酶(AP)偶联链霉亲和素估计检出限为0.03 ng GAD65/ml。新生儿BB/OK大鼠和Lewis大鼠胰岛中GAD65含量分别为37.4和43.7 pg/胰岛。猪脑提取物(55.1 ng/mg蛋白)、小鼠(39.5 ng/mg蛋白)、大鼠(243.8 ng/mg蛋白)、猪小脑提取物(514.8 ng/mg蛋白)以及Lewis大鼠不同脏器提取物中GAD65的定量测定。
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Sensitive monoclonal antibody-based sandwich ELISA for determination of the diabetes-associated autoantigen glutamic acid decarboxylase GAD65.

Although various methods for the detection of autoantibodies against glutamic acid decarboxylase (GAD65-AAb) are known, no sensitive method for the quantification of GAD65 as autoantigen is available. We describe a sandwich ELISA based on monoclonal GAD65 antibodies (Mc-GAD65-Ab) of different epitope specificities to quantify GAD65 in pancreatic islets and in different organ/cell extracts and during the preparation of GAD from brain extracts. GAD65 was captured via solid phase coated Mc-GAD65-Ab and detected via a second biotin-labelled Mc-GAD65-Ab recognizing a NH2-terminal epitope of the molecule. The detection limit was estimated to be 0.03 ng GAD65/ml using alkaline phosphatase (AP)-conjugated streptavidin. GAD65 contents in islets of neonatal BB/OK rats and Lewis rats amounted to 37.4 and 43.7 pg/islet, respectively. Furthermore, GAD65 was quantified in brain extracts of pig (55.1 ng/mg protein), mouse (39.5 ng/mg), rat (243.8 ng/mg) and pig cerebellum (514.8 ng/mg) and in different organ extracts of Lewis rat.

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