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前列环素合成酶活性的放射免疫测定

Radioimmunological assay of prostacyclin synthetase activity.

作者信息

Tai C L, Tai H H

出版信息

Prostaglandins Med. 1980 Jun;4(6):399-408. doi: 10.1016/0161-4630(80)90048-8.

Abstract

A radioimmunoassay for 6-oxoprostaglandin F1 alpha has been developed. 6-Oxoprostaglandin F1 alpha antiplasma was produced in rabbits by repeated immunization with 6-oxoprostaglandin F1 alpha coupled to bovine serum albumin. [125I] -labelled hapten with high specific radioactivity was prepared by radioiodination of 6-oxoprostaglandin F1 alpha-tyrosine methyl ester conjugate followed by purification with thin layer chromatography. The antibodies showed good specificity toward 6-oxoprostaglandin F1 alpha and crossreacted only significantly with prostaglandin F1 alpha. The radioimmunoassay was applied to the determination of prostacyclin synthetase activity in swine aorta microsomes using arachidonic acid and prostaglandin H2 as indirect and direct substrates. The enzyme assay was validated by the criteria that the formation of 6-oxoprostaglandin F1 alpha, immunoreactivity from either substrates was both time and enzyme protein dependent, and was inhibitable by specific inhibitors of the enzyme system.

摘要

已开发出一种用于检测6-氧代前列腺素F1α的放射免疫分析方法。通过用与牛血清白蛋白偶联的6-氧代前列腺素F1α对兔子进行反复免疫,制备了6-氧代前列腺素F1α抗血清。通过对6-氧代前列腺素F1α-酪氨酸甲酯缀合物进行放射性碘化,然后用薄层色谱法纯化,制备了具有高比放射性的[125I]标记半抗原。这些抗体对6-氧代前列腺素F1α显示出良好的特异性,并且仅与前列腺素F1α有显著的交叉反应。使用花生四烯酸和前列腺素H2作为间接和直接底物,将放射免疫分析应用于猪主动脉微粒体中前列环素合成酶活性的测定。通过以下标准验证了酶分析:从两种底物形成的6-氧代前列腺素F1α的免疫反应性均依赖于时间和酶蛋白,并且可被酶系统的特异性抑制剂抑制。

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