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基于生物分子结合域设计的合成发光探针:富含AU的mRNA序列的选择性检测

Design of a synthetic luminescent probe from a biomolecule binding domain: selective detection of AU-rich mRNA sequences.

作者信息

Raibaut Laurent, Vasseur William, Shimberg Geoffrey D, Saint-Pierre Christine, Ravanat Jean-Luc, Michel Sarah L J, Sénèque Olivier

机构信息

Univ. Grenoble Alpes , LCBM/PMB , F-38000 Grenoble , France.

CNRS , LCBM/PMB , UMR 5249 , F-38000 Grenoble , France.

出版信息

Chem Sci. 2017 Feb 1;8(2):1658-1664. doi: 10.1039/c6sc04086a. Epub 2016 Nov 16.

Abstract

We report the design of a luminescent sensor based upon the zinc finger (ZF) protein TIS11d, that allows for the selective time-resolved detection of the UUAUUUAUU sequence of the 3'-untranslated region of messenger RNA. This sensor is composed of the tandem ZF RNA binding domain of TIS11d functionalized with a luminescent Tb complex on one of the ZFs and a sensitizing antenna on the other. This work provides the proof of principle that an RNA binding protein can be re-engineered as an RNA sensor and, more generally, that tunable synthetic luminescent probes for biomolecules can be obtained by modifying biomolecule-binding domains.

摘要

我们报道了一种基于锌指(ZF)蛋白TIS11d的发光传感器的设计,该传感器能够对信使核糖核酸3'非翻译区的UUAUUUAUU序列进行选择性的时间分辨检测。此传感器由TIS11d的串联ZF RNA结合结构域组成,其中一个ZF用发光Tb络合物功能化,另一个ZF上有一个敏化天线。这项工作提供了原理证明,即RNA结合蛋白可以被重新设计为RNA传感器,更普遍地说,可以通过修饰生物分子结合结构域来获得用于生物分子的可调谐合成发光探针。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee39/5364516/0f02c4fe2159/c6sc04086a-f1.jpg

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