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华丽缨鳃虫血红蛋白。I. 亚基相互作用的结构特性与表征

Amphitrite ornata erythrocruorin. I. Structural properties and characterization of subunit interactions.

作者信息

Chiancone E, Brenowitz M, Ascoli F, Bonaventura C, Bonaventura J

出版信息

Biochim Biophys Acta. 1980 May 29;623(1):146-62. doi: 10.1016/0005-2795(80)90017-3.

Abstract

A high molecular weight erythrocruorin (Mr approx. 3 . 10(6)) is found in the vascular system of the marine terebellid worm Amphitrite ornata, while a low molecular weight hemoglobin is contained in the coelomic cells. Polyacrylamide gel electrophoresis indicates that Amphitrite erythrocruorin contains three different types of polypeptide chain, of molecular weight approx. 15,000, whereas the molecular weight per heme group is approx. 20,000. These data suggest that only two of three polypeptide chains may be associated with a heme group. The coelomic hemoglobin, which occurs as a monomer, has an apparent molecular weight of approx. 14,000. The circular dichroism spectra of Amphitrite erythrocruorin and of the coelomic protein reveal marked differences in the heme environment, while the alpha-helical contents are not very different (60% and 70%, respectively). Amphitrite erythrocruorin is unusual in its dissociation behavior. Divalent cations are required for maintaining the quaternary structure. In the pH range 7.75--8.5, when the Ca2+ concentration is reduced below 1 mM, the whole molecule (57 S) dissociates into a number of lower molecular weight species (25, 15, 10 and 3 S) which have been correlated with specific subunit structures by electron microscopy. Whole molecules and 25 S subunits are not in equilibrium with the lower molecular weight species and can be isolated from partially dissociated mixtures. In contrast, the lower molecular weight subunits are themselves in a state of rapid equilibrium which is sensitive to cations, protons and oxygen. Of special interest is the dimerization reaction of the 10 S subunits, which appears to be mediated by Ca2+ and conforms to the predictions of the Cann and Goad theory on ligand mediated equilibria. The dissociation of Amphitrite erythrocruorin is readily reversible when the Ca2+ concentration is increased. The subunits obtained at physiological (7.8) or slightly acid (6.5) pH completely reassemble into whole molecules. Reassembly, however, is only partial when dissociation occurs at high pH. The presence of stable intermediates, such as the 15 S species, may facilitate the reassociation process.

摘要

在海生蛰龙介虫(Amphitrite ornata)的血管系统中发现了一种高分子量的蚯蚓血红蛋白(Mr约为3×10⁶),而在体腔细胞中含有低分子量的血红蛋白。聚丙烯酰胺凝胶电泳表明,蛰龙介虫的蚯蚓血红蛋白含有三种不同类型的多肽链,分子量约为15,000,而每个血红素基团的分子量约为20,000。这些数据表明,三条多肽链中可能只有两条与一个血红素基团相关联。以单体形式存在的体腔血红蛋白的表观分子量约为14,000。蛰龙介虫蚯蚓血红蛋白和体腔蛋白的圆二色光谱显示,血红素环境存在显著差异,而α-螺旋含量差异不大(分别为60%和70%)。蛰龙介虫蚯蚓血红蛋白的解离行为不同寻常。维持四级结构需要二价阳离子。在pH值7.75 - 8.5范围内,当Ca²⁺浓度降至1 mM以下时,整个分子(57 S)会解离成一些低分子量的物种(25、15、10和3 S),通过电子显微镜观察,这些物种与特定的亚基结构相关。完整分子和25 S亚基与低分子量物种并非处于平衡状态,可以从部分解离的混合物中分离出来。相比之下,低分子量亚基本身处于快速平衡状态,对阳离子、质子和氧气敏感。特别有趣的是10 S亚基的二聚化反应,它似乎由Ca²⁺介导,符合坎恩(Cann)和戈德(Goad)关于配体介导平衡的理论预测。当Ca²⁺浓度增加时,蛰龙介虫蚯蚓血红蛋白的解离很容易逆转。在生理pH值(7.8)或微酸性pH值(6.5)下获得的亚基能完全重新组装成完整分子。然而,当在高pH值下发生解离时,重新组装只是部分的。稳定中间体(如15 S物种)的存在可能会促进重新缔合过程。

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