The Francis Crick Institute
Browse
1-s2.0-S2667237523001376-main.pdf (3.61 MB)

Affinity-enhanced RNA-binding domains as tools to understand RNA recognition

Download (3.61 MB)
journal contribution
posted on 2023-07-03, 09:57 authored by Belén Chaves-Arquero, Katherine M Collins, Giancarlo Abis, Geoff Kelly, Evangelos Christodoulou, Ian A Taylor, Andres Ramos
Understanding how the RNA-binding domains of a protein regulator are used to recognize its RNA targets is a key problem in RNA biology, but RNA-binding domains with very low affinity do not perform well in the methods currently available to characterize protein-RNA interactions. Here, we propose to use conservative mutations that enhance the affinity of RNA-binding domains to overcome this limitation. As a proof of principle, we have designed and validated an affinity-enhanced K-homology (KH) domain mutant of the fragile X syndrome protein FMRP, a key regulator of neuronal development, and used this mutant to determine the domain's sequence preference and to explain FMRP recognition of specific RNA motifs in the cell. Our results validate our concept and our nuclear magnetic resonance (NMR)-based workflow. While effective mutant design requires an understanding of the underlying principles of RNA recognition by the relevant domain type, we expect the method will be used effectively in many RNA-binding domains.

Funding

Crick (Grant ID: CC2029, Grant title: Taylor CC2029) Crick (Grant ID: CC1068, Grant title: STP Structural Biology) Crick (Grant ID: CC1078, Grant title: Frenkiel CC1078)

History

Usage metrics

    The Francis Crick Institute

    Licence

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC