Dolashka-Angelova Pavlina, Schwarz Heinz, Dolashki Aleksandar, Stevanovic Stefan, Fecker Miriam, Saeed Muhammad, Voelter Wolfgang
Institute of Organic Chemistry, Bulgarian Academy of Sciences, Sofia, Bulgaria.
Biochim Biophys Acta. 2003 Mar 21;1646(1-2):77-85. doi: 10.1016/s1570-9639(02)00549-6.
The two structural subunits RvH1 and RvH2 were separated after overnight dialysis of Rapana venosa Hc against 130 mM Gly/NaOH buffer, pH 9.6, on an ion exchange column Hiload 26/10 Sepharose Q using a fast performance liquid chromatography (FPLC) system. The reassociation characteristics of these two RvH isoforms and the native molecule were studied in buffers with different pH values and concentrations of Ca(2+) and Mg(2+). Reassociation of mixed RvH subunits was performed over a period of several days using a stabilizing buffer (SB) of pH 7.0 containing different concentrations of Ca(2+) and Mg(2+) ions. After 2 days of dialysis, an RvH subunit mixture of didecamers and multidecamers was observed in the presence of 100 mM CaCl(2) and MgCl(2), though RvH1 and RvH2 are biochemically and immunologically different and have also different dissociation properties. The reassociation, performed at pH 9.6 with 2 mM CaCl(2) and MgCl(2) at 4 degrees C over a period of one to several weeks, led to the formation of decameric oligomers, while didecamers formed predominantly in the SB at pH 7.0. Higher concentrations of calcium and magnesium ions led to a more rapid reassociation of RvH1 resulting in long stable multidecamers and helical tubules, which were stable and slowly dissociated into shorter multidecamers and decamers at higher pH values. The reassociation of the RvH2 structural subunit in the same buffers processed slowly and yielded didecamers, shorter tubule polymers and long multidecamers which are less stable at higher pH values. The stability of RvH isoforms under varying ionic conditions is compared with the stability of keyhole limpet (KLH, Megathura crenulata) hemocyanin (KLH) and Haliotis tuberculata hemocyanin (HtH) isoforms. The process of dissociation and reassociation is connected with changes of the fluorescence intensity at 600 nm, which can be explained by differences in opalescence of the solutions of these two isoforms. The solutions of longer tubule polymers and multidecamers of RvH1 show a higher opalescence compared to the solutions of shorter helical tubules and multidecamers of RvH2.
将脉红螺血蓝蛋白(Rapana venosa Hc)在pH 9.6的130 mM甘氨酸/氢氧化钠缓冲液中过夜透析后,通过快速蛋白质液相色谱(FPLC)系统在离子交换柱Hiload 26/10 Sepharose Q上分离出两个结构亚基RvH1和RvH2。在具有不同pH值以及不同Ca(2+)和Mg(2+)浓度的缓冲液中研究了这两种RvH亚型和天然分子的重新缔合特性。使用含有不同浓度Ca(2+)和Mg(2+)离子、pH 7.0的稳定缓冲液(SB),在几天时间内对混合的RvH亚基进行重新缔合。透析2天后,在存在100 mM CaCl(2)和MgCl(2)的情况下观察到了由双十聚体和多十聚体组成的RvH亚基混合物,尽管RvH1和RvH2在生化和免疫方面存在差异,并且具有不同的解离特性。在pH 9.6、4℃条件下,使用2 mM CaCl(2)和MgCl(2),经过一到几周的时间进行重新缔合,形成了十聚体寡聚物,而在pH 7.0的SB中主要形成双十聚体。较高浓度的钙和镁离子导致RvH1的重新缔合更快,从而形成长的稳定多十聚体和螺旋管,这些在较高pH值下是稳定的,并缓慢解离为较短的多十聚体和十聚体。RvH2结构亚基在相同缓冲液中的重新缔合过程较慢,产生双十聚体、较短的管状聚合物和长的多十聚体,这些在较高pH值下稳定性较差。将不同离子条件下RvH亚型的稳定性与钥孔血蓝蛋白(KLH,Megathura crenulata)和瘤珠鲍血蓝蛋白(HtH)亚型的稳定性进行了比较。解离和重新缔合过程与600 nm处荧光强度的变化有关,这可以通过这两种亚型溶液的乳光差异来解释。与RvH2较短的螺旋管和多十聚体溶液相比,RvH1较长的管状聚合物和多十聚体溶液显示出更高的乳光。