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旋毛虫的热休克蛋白60、热休克蛋白70和热休克蛋白90作为大鼠体液免疫反应的靶点

HSP60, HSP70 and HSP90 from Trichinella spiralis as targets of humoral immune response in rats.

作者信息

Martinez J, Pérez-Serrano J, Bernadina W E, Rodríguez-Caabeiro F

机构信息

Faculty of Pharmacy, University of Alcalá, Madrid, Spain.

出版信息

Parasitol Res. 2001 Jun;87(6):453-8. doi: 10.1007/s004360000315.

Abstract

This study identifies three heat shock proteins (HSPs) using purified preparations from Trichinella spiralis larvae. The proteins: HSP60, HSP70 and HSP90 were found to be targets of the humoral immune response in rats. Three approaches were adopted to obtain T. spiralis HSP-enriched material and/or to purify HSPs to homogeneity. The former product was prepared using affinity chromatography on gelatin sepharose and elution with ATP. Pure 90 kDa-protein was isolated from parasite extract by sequential DEAE (A50) column chromatograpy and preparative electrophoresis. Immunoblot analysis using monoclonal antibodies to HSP60, HSP70 and HSP90 detected the HSP60 and HSP70 in the affinity-purified product and HSP90 in the product obtained by sequential anionic chromatography and preparative electrophoresis. Finally, the reactivy of preimmune, T. spiralis immune and irrelevant immune rat sera on immunoblots were also examined. Only sera taken from infected rats at time-points after day 7 following the first infection exhibited activity against 60, 70 and 90 kDa proteins on blots. The fact that the serum antibodies were anti-HSP was established by immunoadsorption of HSPs to microtiter plates coated with anti-HSP60, anti-HSP70, or anti-HSP90 and using rat sera, positive on blots, to also give positive scores by continued enzyme-linked immunosorbent assay.

摘要

本研究利用旋毛虫幼虫的纯化制剂鉴定出三种热休克蛋白(HSPs)。发现这些蛋白:HSP60、HSP70和HSP90是大鼠体液免疫反应的靶点。采用了三种方法来获得富含旋毛虫HSP的材料和/或将HSP纯化至同质。前一种产物是通过在明胶琼脂糖上进行亲和层析并用ATP洗脱来制备的。通过连续的DEAE(A50)柱层析和制备电泳从寄生虫提取物中分离出纯的90 kDa蛋白。使用针对HSP60、HSP70和HSP90的单克隆抗体进行免疫印迹分析,在亲和纯化产物中检测到HSP60和HSP70,在通过连续阴离子层析和制备电泳获得的产物中检测到HSP90。最后,还检测了免疫前、旋毛虫免疫和无关免疫大鼠血清在免疫印迹上的反应性。只有在首次感染后第7天之后的时间点从感染大鼠采集的血清在印迹上表现出对60、70和90 kDa蛋白的活性。通过将HSP吸附到包被有抗HSP60、抗HSP70或抗HSP90的微量滴定板上,并使用在印迹上呈阳性的大鼠血清通过连续酶联免疫吸附测定也给出阳性分数,从而确定血清抗体为抗HSP这一事实。

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