Legastelois S, Thomas V, Quash G, Métais M P, Tebib J, Moreira A, Monier J C
Laboratoire d'Immunologie, Faculté de Médecine Alexis Carrel, Lyon, France.
J Immunol Methods. 1994 May 2;171(1):111-9. doi: 10.1016/0022-1759(94)90234-8.
The development of a covalent enzyme-linked immunoassay (CELIA) using lipoic acid covalently bound to modified polystyrene microplates has permitted the detection, in the sera of normal BALB/c mice, of natural antibodies reacting with lipoic acid (LA). Hybridomas producing monoclonal anti-LA antibodies were obtained from splenocytes of non-immune BALB/c mice. Two of them, of IgM isotype, recognized LA but failed to react with dihydrolipoic acid (DHLA, the reduced form of LA), suggesting that the integrity of the dithiolane ring was of importance for antibody recognition. They did not give positive reactions with other disulfide linked biological molecules such as oxidized glutathione or cystine. Anti-LA antibodies, coated on polystyrene microplates, were used for the detection of free LA in a competitive assay based on peroxidase-LA conjugate.
利用共价结合到修饰聚苯乙烯微孔板上的硫辛酸开发的共价酶联免疫分析(CELIA),能够在正常BALB/c小鼠血清中检测到与硫辛酸(LA)反应的天然抗体。从非免疫BALB/c小鼠的脾细胞中获得了产生抗LA单克隆抗体的杂交瘤。其中两个IgM同型的杂交瘤识别LA,但不与二氢硫辛酸(DHLA,LA的还原形式)反应,这表明二硫戊环的完整性对于抗体识别很重要。它们与其他二硫键连接的生物分子如氧化型谷胱甘肽或胱氨酸没有阳性反应。包被在聚苯乙烯微孔板上的抗LA抗体用于基于过氧化物酶-LA缀合物的竞争性分析中检测游离LA。