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利用分子识别实现小分子介导的对mRNA翻译的可逆光化学控制。

Harnessing Molecular Recognition for Small-Molecule-Mediated Reversible Photochemical Control Over mRNA Translation.

作者信息

Parmar Shaifaly, Tenney Logan, Liang Xiao, Routzahn John T, Sibley Christopher D, Schneekloth John S

机构信息

Chemical Biology Laboratory, Center for Cancer Research, National Cancer Institute, Frederick, MD 21702-1201, USA.

出版信息

Angew Chem Int Ed Engl. 2025 May 26;64(22):e202503078. doi: 10.1002/anie.202503078. Epub 2025 Apr 22.

Abstract

Chemical probes that control the function of complex RNA molecules offer unique opportunities to interrogate biological systems. In this study, we demonstrate that a small molecule ligand selectively recognizes and undergoes traceless, reversible photocrosslinking to PreQ RNA aptamers. This effect is selective and dependent on both the chemical structure and RNA sequence/structure. A homogeneously modified, caged mRNA construct containing a PreQ aptamer and an eGFP or wild type p53 coding sequence displayed repressed translation in vitro or in cells until irradiated with 302 nm light, resulting in cleavage of the photocage and restoration of translation. This method demonstrates for the first time that aptamer-based molecular recognition of a small molecule ligand can be used to precisely and photochemically activate the translation of a complex mRNA in cells.

摘要

能够控制复杂RNA分子功能的化学探针为研究生物系统提供了独特的机会。在本研究中,我们证明了一种小分子配体能够选择性地识别PreQ RNA适配体,并与之进行无痕、可逆的光交联反应。这种效应具有选择性,并且依赖于化学结构以及RNA序列/结构。一种含有PreQ适配体和增强型绿色荧光蛋白(eGFP)或野生型p53编码序列的均匀修饰的笼化mRNA构建体,在体外或细胞内均表现出翻译抑制,直到用302 nm光照射,导致光笼裂解并恢复翻译。该方法首次证明基于适配体的小分子配体分子识别可用于在细胞中精确地光化学激活复杂mRNA的翻译。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2167/12105704/2da096bf5499/ANIE-64-e202503078-g004.jpg

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