Controlling the Specificity of Modularly Assembled Small Molecules for RNA via Ligand Module Spacing: Targeting the RNAs that Cause Myotonic Muscular Dystrophy

摘要

Myotonic muscular dystrophy types 1 and 2 (DM1 and DM2, respectively) are caused by expansions of repeating nucleotides in non-coding regions of RNA. In DM1, the expansion is an rCUG triplet repeat whereas the DM2 expansion is an rCCUG quadruplet repeat, both of which fold into hairpin structures with periodically repeating internal loops separated by two 5′GC/3′CG base pairs. The sizes of the loops, however, are different: the DM1 repeat forms 1 × 1 nucleotide UU loops while the DM2 repeat forms 2 × 2 nucleotide 5′CU/3′UC loops. DM is caused when the expanded repeats bind the RNA splicing regulator Muscleblind-like 1 protein (MBNL1), thus compromising its function. Therefore, one potential therapeutic strategy for these diseases is to prevent MBNL1 from binding the toxic RNA repeats. Previously, we designed nanomolar inhibitors of the DM2-MBNL1 interaction by modularly assembling 6′-N-5-hexyonate kanamycin A (>K) onto a peptoid backbone. The >K ligand binds the 2 × 2 pyrimidine-rich internal loops found in the DM2 RNA with high affinity. The best compound identified from that study contains three >K modules separated by four propylamine spacing modules and is 20-fold selective over the DM1 RNA. Because the modularly assembled >K-containing compounds also bound the DM1 RNA, albeit with lower affinity, and because the loop size is different, we hypothesized that the optimal DM1 RNA binder may display >K modules separated by shorter distance between ligand modules. Indeed, the ideal DM1 RNA binder has only two propylamine spacing modules separating the >K ligands. Peptoids displaying three and four >K modules on a peptoid scaffold bind the DM1 RNA with Kd's of 20 (3-fold selective for DM1 over DM2) and 4 nM (6-fold selective for DM1 over DM2) and inhibit the RNA-protein interaction with IC50's of 40 and 7 nM, respectively. Importantly, by coupling the two studies together, we have determined that appropriate spacing can affect binding selectivity by 60-fold (20- × 3-fold). The trimer and tetramer also bind ∼13- and ∼63-fold more tightly to DM1 RNAs than does MBNL1. The modularly assembled compounds are cell permeable and non-toxic as determined by flow cytometry. The results establish that for these two systems: (i) a programmable modular assembly approach can provide synthetic ligands for RNA with affinities and specificities that exceed those of natural proteins; and (ii) the spacing of ligand modules can be used to tune specificity for one RNA target over another.