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恶性疟原虫一种通过免疫筛选鉴定出的新型蛋白质Pf62的初步特性分析。

Initial characterization of Pf62, a novel protein of Plasmodium falciparum identified by immunoscreening.

作者信息

Moyano Eva M, González Luis Miguel, Montero Estrella, Cuevas Laureano, Perez-Pastrana Esperanza, Santa-Maria Ysmael, Benito Agustín

机构信息

Centro Nacional de Medicina Tropical, Instituto de Salud Carlos III, Madrid, Spain.

出版信息

Parasitol Res. 2009 Jun;104(6):1389-97. doi: 10.1007/s00436-009-1335-y. Epub 2009 Jan 27.

Abstract

In order to find new antigens from Plasmodium falciparum, a complementary DNA (cDNA) library was constructed and screened. The study of expression library of P. falciparum was performed in an attempt to identify new antigens that could have potential relevance for the falciparum-malaria diagnosis and/or protection. Between the positive clones detected (ring erythrocyte surface antigen, merozoite erythrocyte surface antigen, RHOP H3, CSP, LSA), a new gene that correspond to a new protein (Pf62) was isolated and characterized. This antigen was useful for the diagnosis of malaria in enzyme-linked immunosorbent assay tests. The cDNA corresponding to this antigen and structure of the gene were characterized. Pf62 is a single copy gene that contains one exon. The Pf62 cDNA has an open reading frame of 1,599 nucleotides that code for a putative protein of 532 amino acids with a predicted molecular mass of 62 kDa. The polypeptide contains in the central section two regions of repeats of 21 and 19 amino acids, respectively. The localization of the Pf62 protein was performed by immunoblot, indirect immunofluorescence assay and immunoelectron microscopy. Pf62 is localized in the cytoplasm of the parasite and also on the surface of the infected erythrocyte. Serologic assays by using synthetic peptides designed from different antigenic regions of the Pf62 protein resulted in acceptable data of sensitivity and specificity in symptomatic malaria patients.

摘要

为了从恶性疟原虫中寻找新抗原,构建并筛选了一个互补DNA(cDNA)文库。开展了恶性疟原虫表达文库研究,以鉴定可能与恶性疟疾诊断和/或防护具有潜在相关性的新抗原。在检测到的阳性克隆(环状红细胞表面抗原、裂殖子红细胞表面抗原、RHOP H3、环子孢子蛋白、肝脏特异性抗原)中,分离并鉴定了一个对应新蛋白(Pf62)的新基因。该抗原在酶联免疫吸附测定试验中对疟疾诊断有用。对该抗原对应的cDNA及基因结构进行了鉴定。Pf62是一个单拷贝基因,含有一个外显子。Pf62 cDNA具有一个1599个核苷酸的开放阅读框,编码一个推定的含有532个氨基酸的蛋白,预测分子量为62 kDa。该多肽在中央部分分别包含两个由21个和19个氨基酸组成的重复区域。通过免疫印迹、间接免疫荧光测定和免疫电子显微镜对Pf62蛋白进行定位。Pf62定位于寄生虫的细胞质以及受感染红细胞的表面。使用从Pf62蛋白不同抗原区域设计的合成肽进行血清学检测,在有症状的疟疾患者中获得了可接受的敏感性和特异性数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09f1/2704289/22c5f93cddac/436_2009_1335_Fig1_HTML.jpg

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