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恶性疟原虫表面抗原在大肠杆菌中的表达。

Expression of Plasmodium falciparum surface antigens in Escherichia coli.

作者信息

Ardeshir F, Flint J E, Reese R T

出版信息

Proc Natl Acad Sci U S A. 1985 Apr;82(8):2518-22. doi: 10.1073/pnas.82.8.2518.

Abstract

The asexual blood stages of the human malarial parasite Plasmodium falciparum produce many antigens, only some of which are important for protective immunity. Most of the putative protective antigens are believed to be expressed in schizonts and merozoites, the late stages of the asexual cycle. With the aim of cloning and characterizing genes for important parasite antigens, we used late-stage P. falciparum mRNA to construct a library of cDNA sequences inserted in the Escherichia coli expression vector pUC8. Nine thousand clones from the expression library were immunologically screened in situ with serum from Aotus monkeys immune to P. falciparum, and 95 clones expressing parasite antigens were identified. Mice were immunized with lysates from 49 of the bacterial clones that reacted with Aotus sera, and the mouse sera were tested for their reactivity with parasite antigens by indirect immunofluorescence, immunoprecipitation, and immunoblotting assays. Several different P. falciparum antigens were identified by these assays. Indirect immunofluorescence studies of extracellular merozoites showed that three of these antigens appear to be located on the merozoite surface. Thus, we have identified cDNA clones to three different P. falciparum antigens that may be important in protective immunity.

摘要

人类疟原虫恶性疟原虫的无性血液阶段会产生许多抗原,其中只有一些对保护性免疫很重要。大多数假定的保护性抗原被认为在裂殖体和裂殖子中表达,这是无性周期的后期阶段。为了克隆和鉴定重要寄生虫抗原的基因,我们使用恶性疟原虫后期的mRNA构建了一个插入大肠杆菌表达载体pUC8的cDNA序列文库。用对恶性疟原虫免疫的夜猴血清对来自该表达文库的9000个克隆进行原位免疫筛选,鉴定出95个表达寄生虫抗原的克隆。用与夜猴血清反应的49个细菌克隆的裂解物免疫小鼠,并通过间接免疫荧光、免疫沉淀和免疫印迹分析检测小鼠血清与寄生虫抗原的反应性。通过这些分析鉴定出了几种不同的恶性疟原虫抗原。对细胞外裂殖子的间接免疫荧光研究表明,其中三种抗原似乎位于裂殖子表面。因此,我们已经鉴定出三种不同的恶性疟原虫抗原的cDNA克隆,它们可能在保护性免疫中起重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/977f/397590/83040cfb8c08/pnas00348-0331-a.jpg

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