共查询到18条相似文献,搜索用时 47 毫秒
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用猪甲状腺球蛋白-对氨基苯砜乙基-交联琼脂作亲和吸附剂,可对雪山豆(Phaseolus sp.)凝集素进行亲和层析纯化。纯化后的凝集素在聚丙烯酰胺凝胶电泳中显示单一蛋白质带。Sephadex G-100凝胶层析法测得分子量为65,000道尔顿,SDS-聚丙烯酰胺凝胶电泳表明该凝集素分子仅有一个分子量为65,000道尔顿的亚基,酚-硫酸法测得总糖含量为4.6%,氨基酸组成分析表明雪山豆凝集素富含门冬氨酸,而甲硫氨酸含量甚少。该凝集素是强促有丝分裂原,对人外周血中淋巴细胞的转化率大于90%,细胞分裂比率达12%。雪山豆凝集素不仅能凝集多种动物红细胞,还能凝集人精细胞。经体外实验表明,雪山豆凝集素对人肝癌细胞有抑制作用。 相似文献
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岩豆凝集素(MDL)的远紫外圆二色性谱(CD谱)显示216-217nm处的单一负峰。此时MDL分子含有16.2%的α螺旋,46.3%的β折叠和37.5%的无规卷曲。pH9.0时负峰红移至220nm,且在217-222nm处的峰值几乎相同;在20-40℃范围内,CD谱的变化甚微;60℃时谱峰蓝移;在80℃或100℃时,212nm处出现一大负峰。1mol/L或2mol/L脲时,MDL的CD谱已发生明显 相似文献
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岩豆凝集素的圆二色性与生物学活性关系的研究 总被引:1,自引:0,他引:1
岩豆凝集素(MDL)的远紫外圆二色性谱(CD谱)显示216-217nm处的单一负峰。此时MDL分子含有16.2%的α螺旋,46.3%的β折叠和37.5%的无规卷曲。pH9.0时负峰红移至220nm,且在217-222nm处的峰值几乎相同;在20-40℃范围内,CD谱的变化甚微;60℃时谱峰蓝移;在80℃或100℃时,212nm处出现一大负峰。1mol/L或2mol/L脲时,MDL的CD谱已发生明显变化,二级结构单元也有变化,凝集兔红细胞的活性也随之减弱;随脲浓度的增加,MDL的谱峰蓝移,最终在212nm处出现大负峰。当胍浓度为0.75mol/L时,MDL的CD谱即有明显变化和活性丧失;胍浓度继续增加,CD谱逐渐成为特征的无规卷曲的谱形。在pH9.0、温度超过80℃、脲或胍浓度分别高于2mol/L和0.75mol/L时,MDL的CD谱发生显著变化的同时,其凝集兔红细胞的生物学活性全部丧失,分子的二级结构单元也发生很大改变。 相似文献
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岩豆凝集素分子修饰与圆二色性的关系研究 总被引:1,自引:0,他引:1
天然态岩豆凝集素(MDL)远紫外圆二色性(CD)谱显示216nm处单一负峰,是一种高β-折叠构象凝集素;近紫外CD谱呈现282nm处负峰和260~275nm及295nm处的负肩,经N-乙基顺丁烯二酰亚胺(NEMI)和对氯汞苯甲酸(PCMB)修饰MDL的巯基,其近紫外CD谱未发生变化,远紫外CD谱仅发生细微变化,MDL凝集活性保持不变;PCMB过量时,CD谱呈现典型的无规卷曲谱形,MDL完全丧失凝集活性,去除PCMB后,活性又全部恢复.二硫苏糖醇(DDT)修饰MDL的二硫键并用碘乙酸(ICH2COOH)保护巯基,MDL远紫外CD谱216nm处的负峰红移至225nm,且显著减小;同时,近紫外CD谱282nm处负峰几乎消失,两负肩分别保持完整,分子中α-螺旋降低,无规卷曲增加较多,MDL凝集活性未发生变化.用N-溴代丁二酰亚胺(NBS)修饰MDL分子中的色氨酸,导致216nm负峰蓝移至208nm且变小,分子中无规卷曲和α-螺旋增加,β折叠减少,近紫外CD谱295nm负肩消失,282nm负峰红移至287nm,MDL凝集活性完全丧失. 相似文献
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芦荟凝集素的分离、纯化和部分性质的研究 总被引:5,自引:0,他引:5
新鲜芦荟叶(Aloe vera L.var.chinensis(Haw.)Berger)于室温用低浓度NaCl溶液提取。离心和透析后,经N-乙酰氨基葡萄糖0Sepharose 4B亲和层析,分离纯化出芦荟凝集素(ACL)。用SephadexG-100测表观分子量为35KD,SDS-PAGE出现两条色带;染色 ;宽带和较浅的罕带。亚基分子量分别为15KD和20KD。能专一性凝集兔血细胞和人血红细胞 相似文献
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用猪胃粘蛋白-Sepharose 4B作亲和吸附剂,可从野花生豆(Crotalarta mucronata)的种子中分离纯化出对人类A型血专一凝集的凝集素。该凝集素可用pH30.,Gly-HCl-1mol/L NaCl溶液解吸附。纯化的凝集素在PAGE或SDS-PAGE中均显示单一蛋白带,表明凝集素分子内只有一种亚基。用SDS-PAGE测得其亚基分子量为49,000。氨基酸组成分析表明,该凝集素富含甘氨酸和谷氨酸,不合甲硫氮酸。纯化的野花生豆凝集素(简称CML)含有4.11%的中性糖。它对人A型血细胞有强烈凝集作用,对AB型血有弱凝集作用,但对B型和O型血均不凝集。其对A型血细胞的凝集作用可被N-乙酰半乳糖胺抑制,但对AB型血则无抑制作用。CML是一个促有絲分裂原,对人外周血中淋巴细胞有促有絲分裂作用。 相似文献
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雪山豆凝集素(SML)经SP-Sephadex C-50和磷酸纤维素离子交换层析分离红血球凝集成分。聚丙烯酰胺凝胶电泳分析和红血球凝集试验为一不均一成分。其中E_2-SML有两条迁移较快的蛋白带,红细胞凝集效价是SML的64倍,是L-SML的512倍。该法制备的红细胞凝集成分具有高的产量和纯度。 相似文献
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棉花凝集素的纯化及性质研究 总被引:7,自引:0,他引:7
抗枯萎、抗黄萎病的棉种的浸取液,经硫酸铵分级,纤维素柱、亲和层析后,再经分子筛过滤,获得在PAGE、SDS-PAGE或HPLC柱上均呈现单一蛋白带的棉花凝集素。该凝集素只凝集兔红细胞,对人A、B或O型血细胞均不凝集,其凝集活性可被半乳糖或猪甲状腺球蛋白等所抑制。棉花凝集素在65℃加热5 m in,即丧失全部凝集活性;它的凝集活性强烈地依赖于Ca2+ ;Mn2+ 对活性也有促进作用,Mg2+ 则无作用。经凝胶过滤或SDS-PAGE测定,凝集素的分子量为63000,N-末端氨基酸为Val。凝集素含有1.5% 的中性糖,是一种促有丝分裂原,细胞转化率为50.3% 。 相似文献
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Gao S An J Wu CF Gu Y Chen F Yu Y Wu QQ Bao JK 《Acta biochimica et biophysica Sinica》2005,37(1):47-54
The effects of modifying the carbohydrate chain and amino acids on the conformation and activity of Millettia dielsiana Harms. ex Diels. lectin (MDL) were studied by hemagglutination, fluorescence and circular dichroism analysis. The modification of tryptophan residues led to a compete loss of hemagglutinating activity; however, the addition of mannose was able to prevent this loss of activity. The results indicate that two tryptophan residues are involved in the carbohydrate-binding site. Modifications of the carboxyl group residues produced an 80% loss of activity, but the presence of mannose protected against the modification. The results suggest that the carboxyl groups of aspartic and glutamic acids are involved in the carbohydrate-binding site of the lectin. However, oxidation of the carbohydrate chain and modification of the histidine and arginine residues did not affect the hemagglutinating activity of MDL. Fluorescence studies of MDL indicate that tryptophan residues are present in a relatively hydrophobic region, and the binding of mannose to MDL could quench tryptophan fluorescence without any change in λmax. The circular dichroism spectrum showed that all of these modifications affected the conformation of the MDL molecule to different extents, except the modification of arginine residues. Fluorescence quenching showed that acrylamide and iodoacetic acids are able to quench 77% and 98% of the fluorescence of tryptophan in MDL, respectively. However, KI produced a barely perceptible effect on the fluorescence of MDL, even when the concentration of I^- was 0.15M. This demonstrates that most of tryptophan residues are located in relatively hydrophobic or negatively charged areas near the surface of the MDL molecule. 相似文献
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A lectin with strong hemagglutinating and mitogenic activity was isolated from the seeds of Millettia pachycarpa Benth. by extraction, fraction with (NH4)2 804, ion-exchange chromatography on DEAE-Sepharose and followed by gel filtration on Sephadex G-100. The purified leetin showed a single protein band on PAGE and SDS-PAGE, and exhibited a molecular weight of 40 700 by gel filtration and subunit of 19 800 on SDS-PAGE. It contained 1.78% neutral saceharide and enriched Asp, Glu, Thr, Set, Leu and also contained 4 Trp per molecule. It agglutinated rabbit red cell at 0.48 μg/mL and A,B,O types of blood. The reaction could be inhibited by thyroglobulin, muein gastrie and ovomucin, but not by saceharide. The hemagglutination was strongly dependant on Ca2 +, but was not enhanced by Mg2 + ,Mn2 + ,Zn2 +; The lectin was a strong mitogen for human peripheral blood lymphoeytes, showing a transformation rate and mitotic index of 84.3 % and 7.8 %,respectively. 相似文献
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Defatted seeds of wilt-disease resistant were extracted overnight with PBS at 4 ℃. After centrifugation. 90% saturated (NH4)2SO4 was added to the supernatant. The precipitates were dialysed against H2O, then lyophilized. The purified lectin was obtained by DEAE-cellulose ion-exchange chromatography, Sephadex G-100 filtration, and Sepharose 4B-Hog thyroglohulin affinity chromatography. The activity of the lectin was tested with fresh rabbit erythrocyte in each step of the procedure, and the active part was collected. This sample demonstrated single band on PAGE, SDS-PAGE and HPLC. The lectin was a glycoprotein. It contained 1.5% of neutral saccharide and its molecular weight was 63000 determined by Sephadex G-100 filtration. The N-terminal amino acid of the lectin was Val. The lectin showed no specific agglutination with any type of human erythrocytes. The hemagglutinaition activity could be inhibited by galactose and hog thyroglobilin, and depended on Ca2+, Mn2+, especially on Ca2+, not Mg2+. Its biological activity lost at 65 ℃ for S min. This lectin is used as a mitogen for human peripheral blood lymphocytes. 相似文献
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用Sephadex G-100或猪甲状腺球蛋白-对氨基苯砜乙基-交联琼脂作亲和吸附剂,均可从三齿草藤(Vicia Bungei Ohwi)的种子中分离纯化出三齿草藤凝集素。该凝集素经连续或不连续系统聚丙烯酰胺凝胶电泳均显示出单一蛋白带;糖蛋白染色法证实为糖蛋白;SDS-聚丙烯酰胺凝胶电泳测定其分子量为24,600,凝集素浓度为1.95微克/毫升时就能凝集兔红细胞;但对人ABO型血细胞不发生凝集作用;其对兔红细胞的凝集作用可被D-Man、D-GlcNA和D-GIC所抑制;它也是一种促有丝分裂原。 相似文献
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旋扭山绿豆(Desmodiumintortum)凝集素的纯化与特性彭建宗,程双奇,陈兆平,莫熙穆(华南师范大学生物系,广州510631)关键词凝集素;旋扭山绿豆;亲和层析;糖蛋白豆科植物和根瘤菌之间的共生结瘤固氮关系早有报道。例如大豆只被B.仰。6。... 相似文献
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桑寄生凝集素的纯化及部分性质研究 总被引:1,自引:0,他引:1
利用DEAE一纤维素柱盐离子浓度梯度洗脱,再经猪胃粘蛋白-Sepharose 4 B亲和柱可以从中药桑寄生中分离纯化出桑寄生凝集素。经pH8.9,Tris-EDTAN_2a-borate的PACE和SDS-PAGE测定均呈现单一蛋白带,测得其分子量为67 500,中性糖含量为14.6%,DNS法测得N-末端氨基酸为缬氨酸。氨基酸组成分析表明,该凝集素富含酸性氨基酸,而碱性氨基酸含量较少,不含精氨酸。当凝集素浓度为15.6μg/mL时,即可凝集兔红细胞,而对人的A、B、O型血细胞,凝集素浓度高达1000μg/mL,也不发生凝集反应。Gal、GalNAc、山梨糖、岩藻糖和松三糖对凝集兔红细胞的能力有抑制作用。桑寄生凝集素是一种促有丝分裂原,对猪血淋巴细胞的转化率达78%,细胞分裂比率为11.2%。 相似文献
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香灰菌菌丝体经磷酸缓冲液抽提、20%-70%饱和浓度的硫酸铵沉淀、DEAE-Cellulose和SephadexG-100柱层析纯化得到香灰菌凝集素(Hypoxylonsp.lectin,简称HSL)。HSL经PAGE检测为单一蛋白条带,SDS-PAGE测得其亚基分子量为15.9kD。过碘酸-Schiff染色法表明HSL为一种糖蛋白,糖基的含量为15.5%,β-消去反应测得其糖和蛋白质的连接键为O-型糖肽键。HSL能凝集多种动物红细胞和人的红细胞,在所测试的红细胞中,对兔红细胞的凝集作用最强。HSL对热较敏感,经50°C处理10min,其凝集活性明显降低,其在碱性环境中较稳定,而在酸性环境中较不稳定。HSL的凝集活性受Al3+、Fe3+、Ca2+和Zn2+等阳离子的影响。对鼠红细胞的凝集作用可被半乳糖和乳糖所抑制。 相似文献