Zull J E, Chuang J
Anal Biochem. 1984 Jul;140(1):214-22. doi: 10.1016/0003-2697(84)90157-x.
Highly purified native parathyroid hormone was iodinated by the enzymatic method and separated from unlabeled hormone by isocratic HPLC. The separation system used also resolved iodohistidine, monoiodotyrosine, and diiodotyrosine forms of the hormone from one another. A simplified procedure for direct bioassay of the carrier-free, high specific activity, mono- and diiodinated parathyroid hormone (PTH) by the renal membrane adenylyl cyclase method was also developed. Both labeled forms of the hormone are very potent in this assay, but the iodinated forms appeared to give a lower Vmax than the native hormone. The methods for iodination, separation and biological characterization of this PTH tracer are exceptionally facile, inexpensive, and convenient.
高纯度天然甲状旁腺激素通过酶法进行碘化,并通过等度高效液相色谱法与未标记的激素分离。所使用的分离系统还能将该激素的碘组氨酸、单碘酪氨酸和二碘酪氨酸形式彼此分离。还开发了一种简化程序,通过肾膜腺苷酸环化酶法直接生物测定无载体、高比活性的单碘和二碘甲状旁腺激素(PTH)。该激素的两种标记形式在该测定中都非常有效,但碘化形式的Vmax似乎低于天然激素。这种PTH示踪剂的碘化、分离和生物学特性鉴定方法异常简便、廉价且方便。