生物分子相互作分析技术应用实例（一）：配体垂钓和抗体测定

ＢＩＡ技术－即生物分子相经作用分析技术的应用范围相当广泛,先介绍利用ＢＩＡｃｏｒｅ分离得到ＥＣＫ－酪氨酸激酶受体的蛋白配体。另一应用实例是利用ＢＩＡｃｏｒｅ直接从杂交瘤细胞上清液中测定单克隆抗体的活性、亲和力和动态常数。     

BAS—时间分辨免疫荧光分析检测丙型肝炎抗体

本文介绍将丙肝抗原包被于微量滴定条孔上,使待测丙肝抗体与生物素化抗人ＩｇＧ产生免疫反应,再与Ｅｕ３＋标记的链亲合素产生亲合反应。将ＢＡＳ引入检测方法中,建立了ＢＡＳ－ＴＲＩＦＭＡ检测抗－ＨＣＶ,提高了检测方法的特异性和敏感性     

乙型肝炎病毒e抗原基因与绿色荧光蛋白基因的融合及其表达

质粒pS65T含有T7启动子驱动的绿色荧光蛋白突变型gfpS65T基因,经修饰后,在其中插入乙型肝炎病毒e抗原（HBeAg）基因,使两基因同框成为融合基因。在大肠杆菌BL21中由于T7启动子的控制,高效表达了具有双功能（抗原性和发光性）的融合蛋白（GFP－HBeAg）。融合蛋白MW为52kDa,N端有6个组氨酸残基,因而用Ni金属螯合层析柱对融合蛋白进行了分离纯化,利用诊断HBV的ELISA试剂盒检测了融合蛋白的抗原性,在荧光显微镜下观察到了融合蛋白的绿色荧光。并探讨了用其组装成新型免疫诊断试剂的可能性。     

结香化学成分的研究

从结香(Edgeworthia chrysantha)的花蕾中分离得出3个香豆索,2个黄酮。用波谱等方法确定其结构为伞形花内酯(umbelliferone,1),6-甲氧基-7-羟基双香豆素-3,7’-醚(daphnoretin,2),7,7’-二羟基双香豆素-8,8’-醚-7-α-L-鼠李糖甙(edgeworoside c,5),4’,5,7-三羟基黄酮醇-3-O-β-D-(6′′-对羟基桂皮酰基)-葡萄糖甙(tiliroside,3),山萘酚-3-O-β-D-葡萄糖甙(kaempferol-3-O-β-D-glucoside,4),以上化合物均为首次从结香花蕾中得到。     

大米草对双齿围沙蚕生境中土壤改良作用的研究

大米草对双齿围沙蚕生境中土壤改良作用的研究赵清良赵强（南京师范大学生物系,２１００９７）ＥｆｆｅｃｔｓｏｆＳｐａｒｔｉｎａａｎｇｌｉｃａｔｏｔｈｅＳｏｉｌＨａｂｉｔａｔｓｏｆＰｅｒｅｎｅｒｅｉｓａｉｂｕｈｉｔｅｎｓｉｓ．ＺｈａｏＱｉｎｇｌｉａｎｇ,Ｚ...     

Construction and diversity analysis of a murine IgE phage surface display library

INTR0DUCTI0NIn0urprevi0usstudy0fV5andVKfromfouranti-TCSIgEhybrid0masestab-lishedin0urlaboratory,wefoundVKfr0mallfourcl0nesusedfragmentsfromthesamegermlinegenefamilyVK21,andabiasintheuse0fJk1genefragmentwasalsoobserved.Ontheotherhand,thegeneusageofVHwaJsquitediverse.WespeculatedthatinIgEresponsest0TCS,thelightchainmayplayam0reimpor-tantroleinspecificbindingtoallergenicdeterminant0nTCS[1].However,duet0thelimitationofhybrid0matechnology,itisdifficulttoachievealargenumberofanti-TCSI…     

Human chromosome pellicle antibody recognizing centromere protein—C （CENP0C）,the main component of the kinetochore

Recently the antichromosome antisera from several sclerogerma patients have been found to recognize the pellicle of metaphase and anaphase chromosomes.In order to identify the pellicle components,we used these antichromosome antisera to screen a human embryonic cDNA library.The sequences of the positive clones are identical to the cDNA gene sequence of CENP-C (centromere protein C),a human centromere autoantigen.This result suggusts that CENP-C is a component of the pellicle of human metaphase and anaphase chromosomes.