Thomas T C, Ishikawa Y, McNamee M G, Wilson B W
Department of Biochemistry and Biophysics, University of California, Davis 95616.
Biochem J. 1989 Jan 1;257(1):109-16. doi: 10.1042/bj2570109.
Neuropathy target esterase (NTE) is a membrane-bound carboxylesterase activity that has been proposed as the target site for initiation of organophosphate-induced delayed neuropathy. This activity is identified by its resistance to treatment with Paraoxon and sensitivity to co-incubation with Paraoxon and Mipafox. Sucrose-density-gradient centrifugation of membrane-associated proteins isolated from chick-embryo brains identified three proteins, Mr 161,000, 116,500 and 103,000, that were labelled with [3H]di-isopropyl phosphorofluoridate in an NTE-like manner and that co-migrated with NTE. The 161,000-Mr and 116,500-Mr proteins were identified in both adult and embryo brain. One or both of these proteins may therefore contribute to the activity defined as NTE. In addition, a 61,000-Mr protein was identified that does not comigrate with NTE, but that was labelled with [3H]di-isopropyl phosphorofluoridate in a Paraoxon-resistant and Mipafox-sensitive manner. The effect of Mipafox on labelling, however, was reversibly blocked by co-incubation with Paraoxon. This protein, therefore, is not NTE, but has the necessary inhibitor-sensitivity to be the target site for organophosphate-induced delayed neuropathy.
神经病变靶酯酶(NTE)是一种膜结合羧酸酯酶活性物质,已被认为是有机磷酸酯诱导的迟发性神经病起始的靶位点。这种活性通过其对对氧磷处理的抗性以及与对氧磷和丙胺氟磷共同孵育的敏感性来鉴定。对从鸡胚脑中分离的膜相关蛋白进行蔗糖密度梯度离心,鉴定出三种蛋白,分子量分别为161,000、116,500和103,000,它们以类似NTE的方式被[3H]二异丙基氟磷酸酯标记,并与NTE共同迁移。在成体和胚胎脑中均鉴定出了分子量为161,000和116,500的蛋白。因此,这些蛋白中的一种或两种可能对定义为NTE的活性有贡献。此外,还鉴定出一种分子量为61,000的蛋白,它不与NTE共同迁移,但以对氧磷抗性和丙胺氟磷敏感的方式被[3H]二异丙基氟磷酸酯标记。然而,丙胺氟磷对标记的影响可通过与对氧磷共同孵育而被可逆地阻断。因此,这种蛋白不是NTE,但具有必要的抑制剂敏感性,可成为有机磷酸酯诱导的迟发性神经病的靶位点。