Programmable RNA-binding protein composed of repeats of a single modular unit

被引:49
作者
Adamala, Katarzyna P. [1 ]
Martin-Alarcon, Daniel A. [2 ]
Boyden, Edward S. [1 ,2 ,3 ]
机构
[1] MIT, Media Lab, Cambridge, MA 02139 USA
[2] MIT, Dept Biol Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[3] MIT, Dept Brain & Cognit Sci, McGovern Inst Brain Res, E25-618, Cambridge, MA 02139 USA
基金
美国国家科学基金会;
关键词
RNA-binding protein; Pumilio; gene expression monitoring; protein engineering; translation initiation; PUMILIO-HOMOLOGY DOMAIN; MESSENGER-RNA; LIVING CELLS; MAMMALIAN-CELLS; PUF PROTEINS; FLUORESCENT-PROBES; SPECIFICITY; RECOGNITION; ACTIVATION; SCAFFOLD;
D O I
10.1073/pnas.1519368113
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The ability to monitor and perturb RNAs in living cells would benefit greatly from a modular protein architecture that targets unmodified RNA sequences in a programmable way. We report that the RNA-binding protein PumHD (Pumilio homology domain), which has been widely used in native and modified form for targeting RNA, can be engineered to yield a set of four canonical protein modules, each of which targets one RNA base. These modules (which we call Pumby, for Pumilio-based assembly) can be concatenated in chains of varying composition and length, to bind desired target RNAs. The specificity of such Pumby-RNA interactions was high, with undetectable binding of a Pumby chain to RNA sequences that bear three or more mismatches from the target sequence. We validate that the Pumby architecture can perform RNA-directed protein assembly and enhancement of translation of RNAs. We further demonstrate a new use of such RNA-binding proteins, measurement of RNA translation in living cells. Pumby may prove useful for many applications in the measurement, manipulation, and biotechnological utilization of unmodified RNAs in intact cells and systems.
引用
收藏
页码:E2579 / E2588
页数:10
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