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基于未修饰金纳米粒子选择性聚集的单核苷酸多态性比色基因分型。

Colorimetric genotyping of single nucleotide polymorphism based on selective aggregation of unmodified gold nanoparticles.

机构信息

Department of Chemical and Biomolecular Engineering, Yonsei University, 262 Seongsanno, Seodaemun-gu, Seoul, Republic of Korea.

出版信息

Biosens Bioelectron. 2010 Oct 15;26(2):730-5. doi: 10.1016/j.bios.2010.06.050. Epub 2010 Jul 31.

Abstract

We have developed a colorimetric method for genotyping of single nucleotide polymorphism (rs2131877) in 15 human DNA samples using selective aggregation of unmodified gold nanoparticles. First, we designed two different types of oligonucleotide probes with either thymine or cytosine at the end that are perfect complementary to the target allele sequence. After hybridization of the probe and target DNAs, the double-stranded DNA was added to the unmodified gold nanoparticle suspensions. By adjusting the salt concentration, we could induce aggregation of gold nanoparticles exclusively for the samples with the perfectly matched double-stranded DNAs, which resulted in a distinct color change of the suspension. This enabled us to discern samples with three different genotypes of the target sequences by naked eye: (i) the genotype with only T (thymine) alleles; (ii) that with only C (cytosine) alleles; (iii) that with both T and C alleles. We also confirmed these results by an independent direct sequencing method. These results suggest that the selective aggregation of unmodified gold nanoparticles can successfully be used to discern genotypes of single nucleotide polymorphisms.

摘要

我们开发了一种比色法,用于在 15 个人类 DNA 样本中对单核苷酸多态性(rs2131877)进行基因分型,该方法利用未经修饰的金纳米颗粒的选择性聚集。首先,我们设计了两种不同类型的寡核苷酸探针,其末端要么是胸腺嘧啶,要么是胞嘧啶,与靶等位基因序列完全互补。在探针和靶 DNA 杂交后,将双链 DNA 加入未经修饰的金纳米颗粒悬浮液中。通过调整盐浓度,我们可以仅诱导与完全匹配的双链 DNA 的金纳米颗粒聚集,这导致悬浮液的明显颜色变化。这使我们能够通过肉眼辨别目标序列的三种不同基因型的样本:(i)仅含有 T(胸腺嘧啶)等位基因的基因型;(ii)仅含有 C(胞嘧啶)等位基因的基因型;(iii)同时含有 T 和 C 等位基因的基因型。我们还通过独立的直接测序方法证实了这些结果。这些结果表明,未经修饰的金纳米颗粒的选择性聚集可以成功地用于辨别单核苷酸多态性的基因型。

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