使用基于定制荧光探针的检测方法明确检测 HIV 基因组中的 LTR-III G-四重链。

IF 6.7 1区 化学 Q1 CHEMISTRY, ANALYTICAL
Sumon Pratihar, Vasudhar Bhat S V, Krithi K Bhagavath, Thimmaiah Govindaraju
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引用次数: 0

摘要

病毒病原体基因组中的非规范构象具有重要的诊断价值,这是因为它们具有独特的二级结构,并与特定的荧光分子相互作用。特别是,特定基因序列对 G-四重构象(GQ)的适应会导致不同的拓扑特征,从而形成独特的结合位点,这对小分子选择性识别人类免疫缺陷病毒(HIV)至关重要。利用苯并二噻唑类荧光探针对 LTR-III GQ 靶点的选择性荧光反应,我们开发出了一种基于 GQ 的艾滋病毒检测诊断平台。通过 pH 值控制的 GQ 靶向可靠构象多态性(GQ-RCP),我们成功地荧光识别了包含 LTR-III GQ 的 176 核苷酸扩增基因组片段,从而验证了该方法是一种有效的 GQ 拓扑靶向艾滋病毒诊断工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Unambiguous Detection of LTR-III G-Quadruplex in the HIV Genome Using a Tailored Fluorogenic Probe-based Assay.

Unambiguous Detection of LTR-III G-Quadruplex in the HIV Genome Using a Tailored Fluorogenic Probe-based Assay.

The noncanonical conformations within the genomes of viral pathogens is of significant diagnostic value, due to their unique secondary structures and interactions with specific fluorogenic molecules. In particular, adaptation of the G-quadruplex (GQ) conformation by the specific gene sequence leads to distinct topological features, resulting in unique binding sites that are crucial for the selective recognition of human immunodeficiency virus (HIV) by small molecules. Leveraging the selective fluorescence response of a benzobisthiazole-based fluorogenic probe to the LTR-III GQ target, we developed a GQ-based diagnostic platform for HIV detection. The successful fluorescence recognition of an amplified 176-nucleotide genomic segment harboring the LTR-III GQ, facilitated by pH-controlled GQ-targeted reliable conformational polymorphism (GQ-RCP), validates this method as an effective GQ-topology-targeted diagnostic tool for HIV.

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来源期刊
Analytical Chemistry
Analytical Chemistry 化学-分析化学
CiteScore
12.10
自引率
12.20%
发文量
1949
审稿时长
1.4 months
期刊介绍: Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.
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