Single-molecule study of the CUG repeat-MBNL1 interaction and its inhibition by small molecules

Amin Haghighat Jahromi, Masayoshi Honda, Steven C. Zimmerman, Maria Spies

Research output: Contribution to journalArticle

Abstract

Effective drug discovery and optimization can be accelerated by techniques capable of deconvoluting the complexities often present in targeted biological systems. We report a single-molecule approach to study the binding of an alternative splicing regulator, muscleblind-like 1 protein (MBNL1), to (CUG)n = 4,6 and the effect of small molecules on this interaction. Expanded CUG repeats (CUGexp) are the causative agent of myotonic dystrophy type 1 by sequestering MBNL1. MBNL1 is able to bind to the (CUG) n-inhibitor complex, indicating that the inhibition is not a straightforward competitive process. A simple ligand, highly selective for CUGexp, was used to design a new dimeric ligand that binds to (CUG)n almost 50-fold more tightly and is more effective in destabilizing MBNL1-(CUG)4. The single-molecule method and the analysis framework might be extended to the study of other biomolecular interactions.

Original languageEnglish (US)
Pages (from-to)6687-6697
Number of pages11
JournalNucleic acids research
Volume41
Issue number13
DOIs
StatePublished - Jul 2013

ASJC Scopus subject areas

  • Genetics

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