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本文引用的文献

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Quantifying metabolites using structure-switching aptamers coupled to DNA sequencing.使用与DNA测序相结合的结构转换适体对代谢物进行定量分析。
Nat Biotechnol. 2025 Feb 4. doi: 10.1038/s41587-025-02554-7.
2
Deep generative design of RNA aptamers using structural predictions.使用结构预测进行 RNA 适体的深度生成设计。
Nat Comput Sci. 2024 Nov;4(11):829-839. doi: 10.1038/s43588-024-00720-6. Epub 2024 Nov 6.
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Machine learning guided aptamer refinement and discovery.机器学习指导的适体优化与发现。
Nat Commun. 2021 Apr 22;12(1):2366. doi: 10.1038/s41467-021-22555-9.
4
HMDB 4.0: the human metabolome database for 2018.HMDB 4.0:2018 年人类代谢组数据库。
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Challenges and opportunities for small molecule aptamer development.小分子适配体开发面临的挑战与机遇。
J Nucleic Acids. 2012;2012:748913. doi: 10.1155/2012/748913. Epub 2012 Oct 24.
6
From SOMAmer-based biomarker discovery to diagnostic and clinical applications: a SOMAmer-based, streamlined multiplex proteomic assay.从 SOMAmer 生物标志物发现到诊断和临床应用:基于 SOMAmer 的简化多重蛋白质组分析。
PLoS One. 2011;6(10):e26332. doi: 10.1371/journal.pone.0026332. Epub 2011 Oct 17.
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Aptamer-based multiplexed proteomic technology for biomarker discovery.基于适配体的多重蛋白质组学技术用于生物标志物发现。
PLoS One. 2010 Dec 7;5(12):e15004. doi: 10.1371/journal.pone.0015004.
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High-resolution cross-reactive array for alkaloids.
Chem Commun (Camb). 2009 Jun 14(22):3193-5. doi: 10.1039/b900001a. Epub 2009 May 1.
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Label-free electronic detection of thrombin in blood serum by using an aptamer-based sensor.使用基于适配体的传感器对血清中的凝血酶进行无标记电子检测。
Angew Chem Int Ed Engl. 2005 Aug 26;44(34):5456-9. doi: 10.1002/anie.200500989.
10
Structure-switching signaling aptamers.结构转换信号适配体
J Am Chem Soc. 2003 Apr 23;125(16):4771-8. doi: 10.1021/ja028962o.

迈向基于测序的代谢组学。

Moving towards sequencing-based metabolomics.

作者信息

Clark-ElSayed Alia, Ellington Andrew D, Marcotte Edward M

机构信息

Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA.

Department of Molecular Biosciences, The University of Texas at Austin, Austin, TX, USA.

出版信息

Trends Genet. 2025 Jul;41(7):554-555. doi: 10.1016/j.tig.2025.04.006. Epub 2025 May 6.

DOI:10.1016/j.tig.2025.04.006
PMID:40335328
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12237595/
Abstract

Metabolites are chemically heterogeneous and difficult to quantify in easily read formats. Recently, Tan and Fraser demonstrated that metabolites can be readily quantified by pairing aptamer function with DNA sequencing. This reflects a larger trend of sequencing for assessing biomolecule abundances, further leading to sequencing being a universal analytical tool.

摘要

代谢物在化学性质上具有异质性,并且难以以易于读取的格式进行定量。最近,Tan和Fraser证明,通过将适体功能与DNA测序相结合,可以轻松地对代谢物进行定量。这反映了用于评估生物分子丰度的测序的更大趋势,进一步使测序成为一种通用的分析工具。