Andres R Y, Frei W
Swiss Federal Institute for Reactor Research, Wuerenlingen.
Toxicon. 1987;25(9):915-22. doi: 10.1016/0041-0101(87)90153-x.
A novel approach for the production of [125I]amatoxin and anti-amanitin is described. The antigen and the starting material for Bolton Hunter iodination is prepared by periodic acid oxidation of the gamma-delta-dihydroxy-isoleucine side chain of alpha-amanitin followed by reductive amination. The antigen seems to be of low apparent toxicity. Chemical, spectroscopic and immunological evidence suggests that the hapten has a secondary structure similar to alpha-amanitin, but a modified tryptophanyl ring system. The establishment of a clinically useful iodinated radioimmunoassay system is possible, because the ring system seems to be of limited immunological importance.
描述了一种生产[125I]鹅膏毒素和抗鹅膏蕈碱的新方法。通过对α-鹅膏蕈碱的γ-δ-二羟基异亮氨酸侧链进行高碘酸氧化,然后进行还原胺化反应,制备出用于博尔顿-亨特碘化反应的抗原和起始原料。该抗原的明显毒性似乎较低。化学、光谱和免疫学证据表明,半抗原具有与α-鹅膏蕈碱相似的二级结构,但色氨酸环系统经过了修饰。由于环系统的免疫重要性似乎有限,因此有可能建立一种临床上有用的碘化放射免疫分析系统。