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血清中的促性腺激素受体结合调节剂。促卵泡激素结合抑制剂和促黄体激素结合刺激剂的特性与分离。

Gonadotropin receptor binding regulators in serum. Characterization and separation of follitropin binding inhibitor and lutropin binding stimulator.

作者信息

Sanzo M A, Reichert L E

出版信息

J Biol Chem. 1982 Jun 10;257(11):6033-40.

PMID:6281253
Abstract

Subfractions of human serum capable of inhibiting specific binding of radioiodinated human follitropin and stimulating specific binding of radioiodinated human lutropin to testicular receptors were prepared by molecular sieving techniques, separated by ion exchange chromatography, and further purified by reversed phase high pressure liquid chromatography. Although purified approximately 2000-fold, the exact chemical nature of the follicle-stimulating hormone binding inhibitor is as yet uncertain. However, a variety of analytical procedures indicated it to be separate and distinct from the lutropin binding stimulator, to have a molecular weight of about 700, and to contain a peptide component. Available evidence suggests that the serum factor responsible for luteinizing hormone binding stimulation may be calcium.

摘要

通过分子筛技术制备了能够抑制放射性碘化人促卵泡激素特异性结合并刺激放射性碘化人促黄体生成素与睾丸受体特异性结合的人血清亚组分,经离子交换色谱分离,并通过反相高压液相色谱进一步纯化。尽管已纯化了约2000倍,但促卵泡激素结合抑制剂的确切化学性质仍不确定。然而,多种分析方法表明它与促黄体生成素结合刺激剂不同,分子量约为700,并含有肽成分。现有证据表明,负责刺激促黄体生成素结合的血清因子可能是钙。

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