锌指
核糖核酸
计算生物学
RNA结合蛋白
生物
抄写(语言学)
遗传学
基因
化学
细胞生物学
转录因子
哲学
语言学
作者
Marylène Vandevenne,Mitchell R. O’Connell,Stephanie Helder,Nicholas E. Shepherd,Jacqueline M. Matthews,Ann H. Kwan,David J. Segal,Joel P. Mackay
标识
DOI:10.1002/anie.201402980
摘要
Abstract The realization that gene transcription is much more pervasive than previously thought and that many diverse RNA species exist in simple as well as complex organisms has triggered efforts to develop functionalized RNA‐binding proteins (RBPs) that have the ability to probe and manipulate RNA function. Previously, we showed that the RanBP2‐type zinc finger (ZF) domain is a good candidate for an addressable single‐stranded‐RNA (ssRNA) binding domain that can recognize ssRNA in a modular and specific manner. In the present study, we successfully engineered a sequence specificity change onto this ZF scaffold by using a combinatorial approach based on phage display. This work constitutes a foundation from which a set of RanBP2 ZFs might be developed that is able to recognize any given RNA sequence.
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