Lotan R, Beattie G, Hubbell W, Nicolson G L
Biochemistry. 1977 May 3;16(9):1787-94. doi: 10.1021/bi00628a004.
The effects of several commonly used detergents on the saccharide-binding activities of lectins were investigated using lectin-mediated agglutination of formalin-fixed erythrocytes and affinity chromatography of glycoproteins on columns of lectins immobilized on polyacrylic hydrazide-Sepharose. In the hemagglutination assays, Ricinus communis I (RCA1) and II (RCAII), concanavalin A (Con A), and the agglutinins from peanut (PNA), soybean (SBA), wheat germ (WGA), and Limulus polyphemus (LPA) were tested with several concentrations of switterionic, cationic, anionic, and nonionic detergents. It was found that increasing detergent concentrations eventually affected hemagglutination titers in both test and control samples, and the highest detergent concentrations not affecting lectin hemagglutinating activities were determined. The effects of detergents on specific binding of [3H]fetuin and asialo[3H]fetuin to and elution from columns of immobilized lectins were less severe when compared with lectins in solution, suggesting that the lectins are stabilized by covalent attachment to agarose beads. Nonionic detergents did not affect the binding efficiency of the immobilized lectins tested at concentrations used for membrane solubilization while cationic and zwitterionic detergents caused significant inhibition of Con A- and SBA-Sepharose activities. In sodium deoxycholate (greater than 1%) only RCAI-Sepharose retained its activity, whereas the activities of the other lectins were reduced dramatically. Low concentrations of sodium dodecyl sulfate (0.05%) inhibited only the activity of immobilized SBA, but at higher concentration (0.1%) and prolonged periods of incubation (16 h, 23 degrees C) most of the lectins were inactivated. These data are compared with previous reports on the use of detergents in lectin affinity chromatography, and the conditions for the optimal use of detergents are detailed.
利用凝集素介导的福尔马林固定红细胞的凝集反应以及糖蛋白在固定于聚丙烯酰肼 - 琼脂糖柱上的凝集素柱上的亲和层析,研究了几种常用去污剂对凝集素糖结合活性的影响。在血细胞凝集试验中,用几种浓度的两性离子、阳离子、阴离子和非离子去污剂测试了蓖麻凝集素I(RCA1)和II(RCAII)、伴刀豆球蛋白A(Con A)以及来自花生(PNA)、大豆(SBA)、小麦胚芽(WGA)和鲎(LPA)的凝集素。结果发现,去污剂浓度的增加最终会影响测试样品和对照样品中的血细胞凝集滴度,并确定了不影响凝集素血细胞凝集活性的最高去污剂浓度。与溶液中的凝集素相比,去污剂对[3H]胎球蛋白和去唾液酸[3H]胎球蛋白与固定凝集素柱的特异性结合及从柱上洗脱的影响较小,这表明凝集素通过与琼脂糖珠的共价连接而得以稳定。在用于膜溶解的浓度下,非离子去污剂不影响所测试的固定凝集素的结合效率,而阳离子和两性离子去污剂则显著抑制Con A - 琼脂糖和SBA - 琼脂糖的活性。在脱氧胆酸钠(大于1%)中,只有RCAI - 琼脂糖保留其活性,而其他凝集素的活性则显著降低。低浓度的十二烷基硫酸钠(0.05%)仅抑制固定化SBA的活性,但在较高浓度(0.1%)和延长孵育时间(16小时,23摄氏度)时,大多数凝集素会失活。将这些数据与先前关于在凝集素亲和层析中使用去污剂的报道进行了比较,并详细说明了去污剂最佳使用的条件。