Baigent S M, Lowry P J
School of Animal and Microbial Sciences, University of Reading, Reading, Berkshire RG6 6AJ, UK.
J Mol Endocrinol. 2000 Feb;24(1):53-63. doi: 10.1677/jme.0.0240053.
To purify novel ligands for the corticotrophin-releasing factor binding protein (CRF-BP) from ovine brain, whole brain was homogenised in methanol and the supernatant extracted on Sep-pak C18 cartridges followed by a preliminary HPLC step. Three peaks of ovine CRF-BP ligand activity were detected in the HPLC fractions, the first two of which were also detected by a specific corticotrophin-releasing factor two-site immunoradiometric assay, the third peak being detected by a human CRF-BP ligand assay, which will not detect ovine CRF. Human CRF-BP ligand-containing fractions were further purified by affinity chromatography on a human recombinant CRF-BP column with two additional HPLC steps. The human CRF-BP ligand was found to: (a) possess a molecular mass of 4707 Daltons, (b) have an N-terminal amino acid sequence (5 residues) identical to rat urocortin, (c) be detected by a specific urocortin radioimmunoassay, (d) have high affinity for both the human and ovine CRF-BPs and (e) be present in many regions of the ovine brain. Additionally, a 300 bp cDNA fragment sharing 83% homology with the rat urocortin gene was cloned from ovine brain, the product of which was predicted to have an identical amino acid sequence to that of rat urocortin. These pieces of information confirmed the identity of the human CRF-BP ligand as an ovine urocortin. The specially developed CRF-BP ligand assays showed that the rank orders of affinity of the CRF family members for human CRF-BP were: carp urotensin-1>>human CRF=rat/ovine urocortin>human urocortin>>frog sauvagine>>ovine CRF, and those for the ovine CRF-BP were: carp urotensin-1> human CRF=rat/ovine urocortin>human urocortin> frog sauvagine>>ovine CRF. This study describes a successful technique for the purification and detection of peptide ligands for the CRF-BP. We conclude that urocortin is the principal ligand for the CRF-BP in ovine brain and we could find no evidence for a centrally located mammalian sauvagine-like peptide.
为了从绵羊脑中纯化促肾上腺皮质激素释放因子结合蛋白(CRF-BP)的新型配体,将全脑在甲醇中匀浆,上清液在Sep-pak C18柱上萃取,随后进行初步的高效液相色谱步骤。在高效液相色谱馏分中检测到三个具有绵羊CRF-BP配体活性的峰,其中前两个峰也通过特异性促肾上腺皮质激素释放因子双位点免疫放射测定法检测到,第三个峰通过人CRF-BP配体测定法检测到,该方法不会检测到绵羊CRF。含有人CRF-BP配体的馏分通过在人重组CRF-BP柱上进行亲和层析并结合另外两个高效液相色谱步骤进一步纯化。发现人CRF-BP配体具有以下特性:(a)分子量为4707道尔顿,(b)N端氨基酸序列(5个残基)与大鼠尿皮质素相同,(c)可通过特异性尿皮质素放射免疫测定法检测到,(d)对人和绵羊CRF-BP均具有高亲和力,(e)存在于绵羊脑的许多区域。此外,从绵羊脑中克隆出一个与大鼠尿皮质素基因具有83%同源性的300 bp cDNA片段,预测其产物的氨基酸序列与大鼠尿皮质素相同。这些信息证实了人CRF-BP配体为绵羊尿皮质素。专门开发的CRF-BP配体测定法表明,CRF家族成员对人CRF-BP的亲和力排序为:鲤鱼尿紧张素-1>>人CRF =大鼠/绵羊尿皮质素>人尿皮质素>>青蛙 sauvagine>>绵羊CRF,对绵羊CRF-BP的亲和力排序为:鲤鱼尿紧张素-1>人CRF =大鼠/绵羊尿皮质素>人尿皮质素>青蛙sauvagine>>绵羊CRF。本研究描述了一种成功的技术,用于纯化和检测CRF-BP的肽配体。我们得出结论,尿皮质素是绵羊脑中CRF-BP的主要配体,并且我们没有找到中枢定位的哺乳动物类sauvagine样肽的证据。