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从硬骨鱼杂交条纹鲈中纯化促性腺激素II并开发特异性酶联免疫吸附测定法。

Purification of gonadotropin II from a teleost fish, the hybrid striped bass, and development of a specific enzyme-linked immunosorbent assay.

作者信息

Mañanós E L, Swanson P, Stubblefield J, Zohar Y

机构信息

Center of Marine Biotechnology, University of Maryland Biotechnology Institute, Baltimore, Maryland 21202, USA.

出版信息

Gen Comp Endocrinol. 1997 Nov;108(2):209-22. doi: 10.1006/gcen.1997.6966.

Abstract

A highly purified gonadotropin II (GtH II), referred to as striped bass GtH II (stbGtH II), and its alpha and beta subunits were prepared from pituitaries of sexually mature hybrid striped bass. Pituitary glycoproteins were extracted with ethanol and intact stbGtH II purified by gel-filtration chromatography on Sephadex G-100, ion-exchange chromatography (IEC) on DE-52, and fast-performance liquid chromatography (FPLC) on Superdex 75. The presence of GtHs during the purification procedure was monitored by characteristic elution on reversed-phase high-performance liquid chromatography (rpHPLC) and in vitro steroidogenic activity. The stbGtH II alpha and beta subunits were purified from the pituitary ethanol extract by gel-filtration, IEC, and rpHPLC, and their identities assessed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), rpHPLC, and N-terminal amino acid sequencing. Molecular weights of intact stbGtH II and its alpha and beta subunits, determined by SDS-PAGE, were 34.5, 14.8, and 20.4 kDa, respectively. The stbGtH II beta subunit was used to produce specific antibodies, and a competitive enzyme-linked immunosorbent assay was developed using intact stbGtH II for the standard curve. The sensitivity of the assay was 156 pg/ml (15.6 pg/well) and the intra- and interassay coefficients of variation (at 50% binding) were 7.7% (n = 16) and 8.7% (n = 10), respectively. Physiological validation of the assay was performed by measuring changes of plasma GtH II levels in mature striped bass females, after injection of GnRHa ([d-Ala6,Pro9-NEt]-mGnRH, 100 microg/kg BW). A maximum surge of GtH II in plasma was observed at 12 hr postinjection (22.5 +/- 3. 01 ng/ml), whereas GtH II levels in control fish (around 4 ng/ml) remained unchanged. Displacement curves obtained with serial dilutions of plasma and pituitaries from a number of perciform species were parallel to the standard curve, indicating that this assay can be used for GtH II measurements in a variety of fish species.

摘要

一种高度纯化的促性腺激素II(GtH II),即条纹鲈促性腺激素II(stbGtH II)及其α和β亚基,是从性成熟的杂交条纹鲈的垂体中制备的。垂体糖蛋白用乙醇提取,完整的stbGtH II通过在Sephadex G - 100上的凝胶过滤色谱、在DE - 52上的离子交换色谱(IEC)以及在Superdex 75上的快速高效液相色谱(FPLC)进行纯化。在纯化过程中,通过反相高效液相色谱(rpHPLC)上的特征洗脱和体外类固醇生成活性来监测促性腺激素的存在。stbGtH II的α和β亚基通过凝胶过滤、IEC和rpHPLC从垂体乙醇提取物中纯化出来,并通过十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳(SDS - PAGE)、rpHPLC和N端氨基酸测序来评估其同一性。通过SDS - PAGE测定,完整的stbGtH II及其α和β亚基的分子量分别为34.5、14.8和20.4 kDa。用stbGtH II的β亚基制备特异性抗体,并使用完整的stbGtH II建立标准曲线开发了竞争性酶联免疫吸附测定法。该测定法的灵敏度为156 pg/ml(15.6 pg/孔),批内和批间变异系数(在50%结合率时)分别为7.7%(n = 16)和8.7%(n = 10)。通过测量成熟条纹鲈雌性注射GnRHa([d - Ala6,Pro9 - NEt] - mGnRH,100μg/kg体重)后血浆GtH II水平的变化,对该测定法进行了生理学验证。注射后12小时观察到血浆中GtH II出现最大峰值(22.5±3.01 ng/ml),而对照鱼中的GtH II水平(约4 ng/ml)保持不变。用多种鲈形目物种的血浆和垂体的系列稀释液获得的置换曲线与标准曲线平行,表明该测定法可用于多种鱼类物种中GtH II的测量。

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