婴儿利什曼原虫h3结合ssDNA适体的体外筛选。

Edurne Ramos, Miguel Moreno, M Elena Martín, Manuel Soto, Víctor M Gonzalez
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引用次数: 28

摘要

适配体是单链DNA或RNA寡核苷酸,采用特定的三维结构结合,具有高亲和力和特异性。这些分子目前被用于检测和诊断目的。利什曼原虫属寄生虫在人类和动物中引起利什曼病。有趣的是,利什曼原虫在有丝分裂过程中不浓缩其染色质,组蛋白基因可能是造成这一事实的原因。虽然组蛋白是非常保守的蛋白质,反映了它们明显的功能普世性,但着丝质体核心组蛋白与高等真核生物的序列相似性主要出现在球状区域。然而,n端和c端结构域的高序列差异被发现将它们转化为潜在的诊断和/或治疗靶点。我们已经成功地分离出了一个DNA适体池,命名为SELH3,它与婴儿利什曼原虫H3结合具有高亲和力和特异性。因此,这种新型抗h3适体群体可能具有潜在的应用价值,可作为利什曼病的诊断系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vitro selection of Leishmania infantum H3-binding ssDNA aptamers.

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.

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来源期刊
Oligonucleotides
Oligonucleotides 生物-生化与分子生物学
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