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婴儿利什曼原虫 H3 结合单链 DNA 适配体的体外筛选

In vitro selection of Leishmania infantum H3-binding ssDNA aptamers.

作者信息

Ramos Edurne, Moreno Miguel, Martín M Elena, Soto Manuel, Gonzalez Víctor M

机构信息

Departamento de Bioquímica-Investigación, Instituto Ramón y Cajal de Investigación Sanitaria, Madrid, Spain.

出版信息

Oligonucleotides. 2010 Aug;20(4):207-13. doi: 10.1089/oli.2010.0240.

Abstract

Aptamers are single-stranded DNA or RNA oligonucleotides that adopt specific three-dimensional structures binding with high affinity and specificity to their targets. These molecules are being currently used with detection and diagnosis purposes. Parasites of the genus Leishmania cause leishmaniosis in humans and animals. Interestingly, Leishmania do not condense their chromatin during mitosis, and histone genes could be responsible for this fact. Although histones are extremely conserved proteins, reflecting their apparent universality of function, sequence similarity of kinetoplastid core histones with that of higher eukaryotes is found predominantly in the globular region. However, high sequence divergences in the N-terminal and C-terminal domains are found that convert them into potential diagnostic and/or therapeutics targets. We have successfully isolated a pool of DNA aptamers, named SELH3, which binds to Leishmania infantum H3 with high affinity and specificity. Thus, it appears that this novel anti-H3 aptamer population may be of potential application as a diagnostic system for leishmaniosis.

摘要

适体是单链DNA或RNA寡核苷酸,它们能形成特定的三维结构,以高亲和力和特异性与其靶标结合。目前这些分子正用于检测和诊断目的。利什曼原虫属的寄生虫可导致人类和动物患利什曼病。有趣的是,利什曼原虫在有丝分裂期间不会浓缩其染色质,组蛋白基因可能是导致这一现象的原因。尽管组蛋白是极其保守的蛋白质,这反映了它们功能上明显的普遍性,但动质体核心组蛋白与高等真核生物的序列相似性主要存在于球状区域。然而,在N端和C端结构域发现了高度的序列差异,这使它们成为潜在的诊断和/或治疗靶点。我们成功分离出一组名为SELH3的DNA适体,它能以高亲和力和特异性与婴儿利什曼原虫的H3结合。因此,这种新型抗H3适体群体似乎有可能作为利什曼病的诊断系统应用。

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