Adamala Katarzyna P, Martin-Alarcon Daniel A, Boyden Edward S
Media Lab, Massachusetts Institute of Technology, Cambridge, MA 02139;
Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139;
Proc Natl Acad Sci U S A. 2016 May 10;113(19):E2579-88. doi: 10.1073/pnas.1519368113. Epub 2016 Apr 26.
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.
能够在活细胞中监测和干扰RNA将极大地受益于一种模块化蛋白质结构,该结构能够以可编程的方式靶向未修饰的RNA序列。我们报告称,RNA结合蛋白PumHD(Pumilio同源结构域),已以天然和修饰形式广泛用于靶向RNA,可进行工程改造以产生一组四个典型蛋白质模块,每个模块靶向一个RNA碱基。这些模块(我们称之为Pumby,基于Pumilio的组装)可以连接成不同组成和长度的链,以结合所需的靶RNA。这种Pumby-RNA相互作用的特异性很高,Pumby链与与靶序列有三个或更多错配的RNA序列之间未检测到结合。我们验证了Pumby结构可以进行RNA指导的蛋白质组装并增强RNA的翻译。我们进一步证明了这种RNA结合蛋白的一种新用途,即测量活细胞中的RNA翻译。Pumby可能在完整细胞和系统中未修饰RNA的测量、操作和生物技术利用的许多应用中证明是有用的。