Cunningham B C, Mulkerrin M G, Wells J A
Department of Protein Engineering, Genentech, South San Francisco, CA 94080.
Science. 1991 Aug 2;253(5019):545-8. doi: 10.1126/science.1907025.
Size-exclusion chromatography and sedimentation equilbrium studies demonstrated that zinc ion (Zn2+) induced the dimerization of human growth hormone (hGH). Scatchard analysis of 65Zn2+ binding to hGH showed that two Zn2+ ions associate per dimer of hGH in a cooperative fashion. Cobalt (II) can substitute for Zn2+ in the hormone dimer and gives a visible spectrum characteristic of cobalt coordinated in a tetrahedral fashion by oxygen- and nitrogen-containing ligands. Replacement of potential Zn2+ ligands (His18, His21, and Glu174) in hGH with alanine weakened both Zn2+ binding and hGH dimer formation. The Zn(2+)-hGH dimer was more stable than monomeric hGH to denaturation in guanidine-HCl. Formation of a Zn(2+)-hGH dimeric complex may be important for storage of hGH in secretory granules.
尺寸排阻色谱法和沉降平衡研究表明,锌离子(Zn2+)可诱导人生长激素(hGH)二聚化。对65Zn2+与hGH结合的斯卡查德分析表明,每二聚体hGH中有两个Zn2+离子以协同方式结合。钴(II)可在激素二聚体中替代Zn2+,并给出由含氧化合物和含氮配体以四面体方式配位的钴的可见光谱特征。用丙氨酸替代hGH中潜在的Zn2+配体(His18、His21和Glu174)会削弱Zn2+结合和hGH二聚体形成。Zn(2+)-hGH二聚体在盐酸胍中比单体hGH对变性更稳定。形成Zn(2+)-hGH二聚体复合物可能对hGH在分泌颗粒中的储存很重要。