Devolder A, Renaville R, Sneyers M, Callebaut I, Massart S, Goffinet A, Burny A, Portetelle D
Molecular Biology and Animal Physiology Unit, Faculty of Agronomy, Gembloux, Belgium.
J Endocrinol. 1993 Jul;138(1):91-8. doi: 10.1677/joe.0.1380091.
The presence of GH-binding proteins (GHBPs) in the plasma of adult cattle was investigated using Sephadex G-200 filtration, Western ligand blotting and Western blotting. The changes in the concentration of GHBP in the plasma of dairy half-sister heifers during the first year of life as well as the presence of GHBP in milk were also investigated. When analytical chromatography (on a 1.6 x 100 cm column) was performed, five peaks of recombinant bovine GH (rbGH)-associated radioactivity were revealed in cattle plasma; the first peak, which appeared near the void volume, was presumed to represent aggregates, the second (M(r) 290 kDa) and the third peaks (M(r) 75 kDa) corresponded to specific rbGH-GHBP complexes; the last two peaks representing free 125I-labelled rbGH and Na[125I]. Western ligand blotting revealed multiple GHBPs. Three major bands were observed at approximately 190, 58 and 31 kDa; an excess of unlabelled hormone blocked the binding of 125I-labelled rbGH. Minor non-specific binding bands were also detected in cattle plasma with molecular weights between 40 and 136 kDa. One monoclonal antibody (8H7) produced against synthetic peptide (amino acids 54-63 of the extracellular domain of the bovine GH receptor) specifically interacted with 190 and 58 kDa bands while the 31 kDa band was not recognized. Finally, Western ligand blots were performed to evaluate the changes in plasma GHBP during the first year of life in 55 dairy half-sister heifers and to identify GHBP in milk. In plasma, the intensity of the 31 kDa band varied greatly between animals while the other specific bands remained stable.(ABSTRACT TRUNCATED AT 250 WORDS)
采用葡聚糖凝胶G - 200过滤、Western配体印迹法和Western印迹法,对成年牛血浆中生长激素结合蛋白(GHBPs)的存在情况进行了研究。同时还研究了半同胞奶牛小母牛出生后第一年血浆中GHBP浓度的变化以及牛奶中GHBP的存在情况。进行分析色谱法(在1.6×100 cm柱上)时,在牛血浆中发现了五个与重组牛生长激素(rbGH)相关的放射性峰;第一个峰出现在空体积附近,推测代表聚集体,第二个峰(M(r) 290 kDa)和第三个峰(M(r) 75 kDa)对应于特定的rbGH - GHBP复合物;最后两个峰代表游离的125I标记的rbGH和Na[125I]。Western配体印迹法显示存在多种GHBPs。观察到三条主要条带,分子量约为190、58和31 kDa;过量的未标记激素可阻断125I标记的rbGH的结合。在牛血浆中还检测到分子量在40至136 kDa之间的次要非特异性结合条带。一种针对合成肽(牛生长激素受体细胞外结构域的氨基酸54 - 63)产生的单克隆抗体(8H7)与190和58 kDa条带特异性相互作用,而31 kDa条带未被识别。最后,进行Western配体印迹法以评估55头半同胞奶牛小母牛出生后第一年血浆中GHBP的变化,并鉴定牛奶中的GHBP。在血浆中,31 kDa条带的强度在不同动物之间差异很大,而其他特异性条带保持稳定。(摘要截短至250字)