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用于改善靶标识别和生物标志物检测的交联剂修饰核酸探针。

Crosslinker-modified nucleic acid probes for improved target identification and biomarker detection.

作者信息

Elskens Joke, Madder Annemieke

机构信息

Department of Organic and Macromolecular Chemistry, Faculty of Sciences, Ghent University Krijgslaan 281 Building S4 9000 Ghent Belgium

出版信息

RSC Chem Biol. 2021 Feb 22;2(2):410-422. doi: 10.1039/d0cb00236d. eCollection 2021 Apr 1.

Abstract

Understanding the intricate interaction pattern of nucleic acids with other molecules is essential to gain further insight in biological processes and disease mechanisms. To this end, a multitude of hybridization-based assays have been designed that rely on the non-covalent recognition between complementary nucleic acid sequences. However, the ephemeral nature of these interactions complicates straightforward analysis as low efficiency and specificity are rule rather than exception. By covalently locking nucleic acid interactions by means of a crosslinking agent, the overall efficiency, specificity and selectivity of hybridization-based assays could be increased. In this mini-review we highlight methodologies that exploit the use of crosslinker-modified nucleic acid probes for interstrand nucleic acid crosslinking with the objective to study, detect and identify important targets as well as nucleic acid sequences that can be considered relevant biomarkers. We emphasize on the usefulness and advantages of crosslinking agents and elaborate on the chemistry behind the crosslinking reactions they induce.

摘要

了解核酸与其他分子之间复杂的相互作用模式对于深入洞察生物过程和疾病机制至关重要。为此,已经设计了多种基于杂交的检测方法,这些方法依赖于互补核酸序列之间的非共价识别。然而,这些相互作用的短暂性使得直接分析变得复杂,因为低效率和低特异性是常态而非例外。通过使用交联剂共价锁定核酸相互作用,可以提高基于杂交的检测方法的整体效率、特异性和选择性。在本综述中,我们重点介绍了利用交联剂修饰的核酸探针进行链间核酸交联的方法,目的是研究、检测和识别重要靶点以及可被视为相关生物标志物的核酸序列。我们强调交联剂的有用性和优势,并详细阐述它们所诱导的交联反应背后的化学原理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be91/8341421/ee18ff4010bf/d0cb00236d-f1.jpg

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