A new approach of indirect enzyme-linked immunosorbent assay for determination of D-glutamic acid through in situ conjugation

S. Sakamoto, R. Nagamitsu, Yurino Matsuura, Y. Tsuneura, H. Kurose, Hiroyuki Tanaka, S. Morimoto
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Abstract

We propose a new approach of an indirect enzyme-linked immunosorbent assay (ELISA) for determination of D-glutamic acid (D-Glu) using a monoclonal antibody against D-glutamic acid (D-Glu-MAb), which recognizes D-Glu-glutaraldehyde (GA) molecule but not D-Glu molecule. Human serum albumin (HSA) was coated on an immunoplate and reacted with D-Glu via GA to produce D-Glu-GA-HSA conjugates in situ in the well to be recognized by D-Glu-MAb, which enabled the development of an indirect ELISA for the determination of free D-Glu. In this indirect ELISA, D-Glu can be specifically detected with limit of detection of 7.81 μg/mL. Since anti-conjugate antibodies are often produced, even though anti-hapten antibodies are desired, this new approach could be very useful as an application of anti-conjugate antibodies to the development of quantitative analysis for detecting hapten.
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原位偶联间接酶联免疫吸附法测定d -谷氨酸的新方法
我们提出了一种间接酶联免疫吸附法(ELISA)检测d -谷氨酸(D-Glu)的新方法,该方法使用抗d -谷氨酸单克隆抗体(D-Glu- mab),该抗体识别d -谷氨酸-戊二醛(GA)分子而不识别d -谷氨酸分子。将人血清白蛋白(Human serum albumin, HSA)包被在免疫板上,通过GA与D-Glu反应,在孔中原位生成D-Glu-GA-HSA偶联物,可被D-Glu- mab识别,从而建立了间接ELISA法测定游离D-Glu。该间接ELISA法特异性检测D-Glu,检出限为7.81 μg/mL。由于经常产生抗偶联抗体,即使需要抗半抗原抗体,这种新方法可以作为抗偶联抗体在半抗原检测定量分析发展中的应用非常有用。
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