Roy S, Michaelis E K
J Neurochem. 1984 Mar;42(3):838-41. doi: 10.1111/j.1471-4159.1984.tb02757.x.
Antibodies against the purified bovine brain glutamate binding protein (GBP) were raised in rabbits. Both nonderivatized and dinitrobenzene-derivatized GBP produced strong immunological responses in rabbits. Using the enzyme-linked immunosorbent assay (ELISA), we have quantified the antibody production and determined the specificity of the antibodies. Bovine brain GBP and the analogous protein from rat brain interacted most strongly with the antibodies. A bacterial glutamate-aspartate binding protein, as well as the enzymes glutamate dehydrogenase (EC 1.4.1.3), glutamine synthetase (EC 6.3.1.2), and gamma-glutamyl transpeptidase (EC 2.3.2.2), showed little or no cross-reactivity with the anti-GBP antibodies. A crude bacterial glutamate decarboxylase (EC 4.1.1.15) preparation gave a small to moderate cross-reaction with the anti-GBP antibodies. The sensitivity of the ELISA assay and the specificity of the antibodies were such that GBP levels as low as 3-10 ng could be detected.
在兔体内产生了针对纯化牛脑谷氨酸结合蛋白(GBP)的抗体。未衍生化和二硝基苯衍生化的GBP在兔体内均产生强烈的免疫反应。使用酶联免疫吸附测定(ELISA),我们对抗体产生进行了定量,并确定了抗体的特异性。牛脑GBP和大鼠脑的类似蛋白与抗体的相互作用最强。一种细菌谷氨酸-天冬氨酸结合蛋白,以及谷氨酸脱氢酶(EC 1.4.1.3)、谷氨酰胺合成酶(EC 6.3.1.2)和γ-谷氨酰转肽酶(EC 2.3.2.2)与抗GBP抗体几乎没有或没有交叉反应。粗制的细菌谷氨酸脱羧酶(EC 4.1.1.15)制剂与抗GBP抗体有小到中等程度的交叉反应。ELISA测定的灵敏度和抗体的特异性使得低至3 - 10 ng的GBP水平都能被检测到。