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从多毛纲环节动物华丽盘管虫中分离并鉴定一种血凝素

Isolation and characterization of a hemagglutinin from Amphitrite ornata, a polychaetous annelid.

作者信息

Garte S J, Rissell C S

出版信息

Biochim Biophys Acta. 1976 Aug 9;439(2):368-79. doi: 10.1016/0005-2795(76)90073-8.

Abstract

Extracts of the marine polychaetous annelid, Amphitrite ornata, agglutinate rat, rabbit, chicken and human erythrocytes and in other work have been shown to inhibit the growth of Ehrlich ascites tumors in mice. Fractionation of extracts on Sephadex G-100 gave three active fractions with molecular weights of 30 000, 54 000 and 100 000. The 30 000 dalton fraction (B) was purified 72-fold by ammonium sulfate precipitation, gel filtration and preparative disc gel electrophoresis. The purified hemagglutinin, amphitritin, was homogenous on analytical disc gel electrophoresis at four different pH values and gave a sharp boundary in sedimentation velocity ultracentrifugation. The three fractions showed paralled specificity toward rat and chicken erythrocytes, the former giving the higher titer. The purified agglutinin was active toward human blood groups A, B and O and exhibited 4-fold higher activity toward group A. The hemagglutinin titer against rat red blood cells was lowered only by N-acetylgalactosamine, the terminal sugar residue of the group A determinant. None of the saccharides tested inhibited agglutination of chicken erythrocytes. Hemagglutinin activity was insensitive to dialysis or treatment with EDTA. The activity was not affected by digestion with trypsin or pronase, but was destroyed by phenol extraction. Analytical disc gel electrophoresis showed one protein band with high anodal mobility at pH 8.5, which was not affected by proteolytic enzymes but was removed by phenol. Activity was unaffected by heating at 70 degrees C for 30 min but was destroyed by similar treatemtn at 85 degrees C. Activity was at a maximum at pH 7-9 and decreased reversibly down to pH 4 at which point it was irreversibly inactivated. The higher molecular weight agglutinin (A1) could be dissociated to give amphitritin by treatment with 6M urea of precipitation in 55% (NH4)2SO4. This dissociation was not reversed by dialysis. Amphitritin is a glycoprotein with a molecular weight determined by gel filtration of 30 000 and by approach to equilibrium sedimentation of 32 000. Amino acid analysis showed a preponderance of aspartic and glutamic acids and relatively large amounts of glycine, proline, alanine, valine and cysteine. The carbohydrate moeity which represented 12.8% of the molecule, contained mannose, galactose, glucosamine and sialic acid. Amphitritin is the first hemagglutinin to be isolated from a polychaetous annelid.

摘要

海洋多毛纲环节动物华丽盘管虫(Amphitrite ornata)的提取物能凝集大鼠、兔子、鸡和人类的红细胞,并且在其他研究中已表明其能抑制小鼠艾氏腹水瘤的生长。将提取物在葡聚糖G - 100上进行分级分离得到了三个活性级分,分子量分别为30000、54000和100000。通过硫酸铵沉淀、凝胶过滤和制备性圆盘凝胶电泳,将30000道尔顿的级分(B)纯化了72倍。纯化后的血凝素——盘管虫素,在四种不同pH值下的分析性圆盘凝胶电泳中均表现为均一性,并且在沉降速度超速离心中呈现出清晰的边界。这三个级分对大鼠和鸡的红细胞表现出相似的特异性,对前者的凝集效价更高。纯化后的凝集素对人类A、B和O血型均有活性,对A血型的活性高出4倍。针对大鼠红细胞的血凝效价仅被A血型决定簇的末端糖残基N - 乙酰半乳糖胺降低。所测试的糖类均未抑制鸡红细胞的凝集。血凝素活性对透析或用EDTA处理不敏感。该活性不受胰蛋白酶或链霉蛋白酶消化的影响,但会被苯酚提取破坏。分析性圆盘凝胶电泳显示在pH 8.5时出现一条具有高阳极迁移率的蛋白带(该蛋白带不受蛋白水解酶影响,但可被苯酚去除)。70℃加热30分钟活性不受影响,但85℃进行类似处理则会破坏活性。活性在pH 7 - 9时最高,在pH 4时可逆下降,此时会不可逆失活。通过用6M尿素处理或在55%硫酸铵中沉淀,较高分子量的凝集素(A1)可解离产生盘管虫素。这种解离不能通过透析逆转。盘管虫素是一种糖蛋白,通过凝胶过滤测定其分子量为30000,通过平衡沉降法测定为32000。氨基酸分析表明天冬氨酸和谷氨酸占优势,并且含有相对大量的甘氨酸、脯氨酸、丙氨酸、缬氨酸和半胱氨酸。占分子12.8%的碳水化合物部分含有甘露糖、半乳糖、葡糖胺和唾液酸。盘管虫素是首个从多毛纲环节动物中分离得到的血凝素。

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