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隐孢子虫卵囊的电泳和免疫印迹分析。

Electrophoretic and immunoblot analysis of Cryptosporidium oocysts.

作者信息

Lumb R, Lanser J A, O'Donoghue P J

机构信息

Division of Clinical Microbiology, Institute of Medical and Veterinary Science, Adelaide, SA, Australia.

出版信息

Immunol Cell Biol. 1988 Oct-Dec;66 ( Pt 5-6):369-76. doi: 10.1038/icb.1988.48.

Abstract

Cryptosporidium oocysts were recovered by density gradient centrifugation from diarrhoeal faeces of four human patients and one goat kid. Goat-derived oocysts were further treated with excystation medium and the excysted oocyst walls purified by isopycnic ultracentrifugation. Soluble extracts from intact oocysts and the oocyst wall preparation were analysed by SDS-PAGE. Fifty-one polypeptide bands were detected in intact oocyst preparations: 48 were in the range 14,000-200,000 molecular weight (MW), two bands were less than 14,000 MW and one band was above 200,000 MW. Twenty-one bands were detected in the oocyst wall preparation, all within the range 14,000-200,000 MW. Immunoblot analysis of Cryptosporidium polypeptides using acute or convalescent human and goat sera revealed a large number of reactive bands. Varying degrees of heterogeneity were observed within and between the two serum groups. Nine of the 10 human sera and all of the goat kid sera reacted with a 23,000 MW and 32,000 MW antigen. A 15,500 MW antigen was also detected by all the goat and four of the 10 human sera. Both serum groups reacted with various antigens above 40,000 MW. Surface labelling of three human isolates of Cryptosporidium oocysts with 125I was performed using the Bolton and Hunter reagent. The solubilized preparations were separated by SDS-PAGE on 12% and 18% slab gels and autoradiographed. Common bands were seen at 15,500, 32,000, 47,500, 79,000 and 96,000 MW. Some variation in the molecular weight of polypeptides labelled with 125I was observed among the three isolates.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过密度梯度离心法从4名人类患者和1只山羊幼崽的腹泻粪便中回收了隐孢子虫卵囊。将源自山羊的卵囊用脱囊培养基进一步处理,并通过等密度超速离心法纯化脱囊后的卵囊壁。通过SDS-PAGE分析完整卵囊和卵囊壁制剂的可溶性提取物。在完整卵囊制剂中检测到51条多肽带:48条在分子量(MW)14,000-200,000范围内,2条带小于14,000 MW,1条带高于200,000 MW。在卵囊壁制剂中检测到21条带,均在14,000-200,000 MW范围内。使用急性或恢复期人类和山羊血清对隐孢子虫多肽进行免疫印迹分析,发现大量反应性条带。在两个血清组内和组间观察到不同程度的异质性。10份人类血清中的9份和所有山羊幼崽血清与23,000 MW和32,000 MW抗原发生反应。所有山羊血清和10份人类血清中的4份也检测到15,500 MW抗原。两个血清组均与40,000 MW以上的各种抗原发生反应。使用博尔顿和亨特试剂对3株人类隐孢子虫卵囊进行125I表面标记。将溶解的制剂在12%和18%的平板凝胶上通过SDS-PAGE分离并进行放射自显影。在15,500、32,000、47,500、79,000和96,000 MW处可见共同条带。在这三株分离株中观察到用125I标记的多肽分子量存在一些差异。(摘要截断于250字)

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