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微小隐孢子虫子孢子15千道尔顿和60千道尔顿蛋白共有的表位编码cDNA的克隆与表达

Cloning and expression of a cDNA encoding epitopes shared by 15- and 60-kilodalton proteins of Cryptosporidium parvum sporozoites.

作者信息

Jenkins M C, Fayer R, Tilley M, Upton S J

机构信息

Protozoan Diseases Laboratory, U.S. Department of Agriculture, Beltsville, Maryland 20705.

出版信息

Infect Immun. 1993 Jun;61(6):2377-82. doi: 10.1128/iai.61.6.2377-2382.1993.

Abstract

A cDNA (CP15/60) encoding epitopes of Cryptosporidium parvum 15- and 60-kDa sporozoite proteins was isolated and expressed in Escherichia coli toward the goal of developing an immunogen for producing high-titer anticryptosporidial colostrum. Antisera prepared in rats to native C. parvum 15-kDa protein and used to identify the CP15/60 bacteriophage clone recognized both 15- and 60-kDa in vitro translation products derived from sporozoite RNA. Antisera specific for recombinant CP15/60 antigen recognized native 15- and 60-kDa C. parvum sporozoite proteins by immunoblotting and identified both surface and internal antigens on C. parvum sporozoites by immunofluorescence staining. Northern (RNA) and Southern blot hybridization experiments using sporozoite RNA and DNA indicated that CP15/60 DNA is transcribed as a single 1.4-kb RNA species from a single-copy gene. Recombinant CP15/60 antigen was recognized by hyperimmune colostrum from cows immunized with C. parvum oocyst-sporozoite protein and by convalescent-phase sera from C. parvum-infected calves.

摘要

分离出编码微小隐孢子虫15 kDa和60 kDa子孢子蛋白表位的cDNA(CP15/60),并在大肠杆菌中表达,目的是开发一种免疫原,用于生产高滴度的抗隐孢子虫初乳。用天然微小隐孢子虫15 kDa蛋白在大鼠中制备抗血清,用于鉴定CP15/60噬菌体克隆,该克隆在体外识别源自子孢子RNA的15 kDa和60 kDa翻译产物。针对重组CP15/60抗原的抗血清通过免疫印迹识别天然微小隐孢子虫15 kDa和60 kDa子孢子蛋白,并通过免疫荧光染色鉴定微小隐孢子虫子孢子表面和内部的抗原。使用子孢子RNA和DNA进行的Northern(RNA)和Southern印迹杂交实验表明,CP15/60 DNA从单拷贝基因转录为单一的1.4 kb RNA种类。重组CP15/60抗原被用微小隐孢子虫卵囊-子孢子蛋白免疫的奶牛的高免疫初乳以及微小隐孢子虫感染小牛的恢复期血清识别。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b9e/280858/0a9123be9e5e/iai00018-0121-a.jpg

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