The rapidly expanding database of RNA structures and protein complexes is b
eginning to lead to the successful design of specific RNA-binding molecules
. Recent combinatorial and structure-based approaches have utilized known n
ucleic-acid-binding scaffolds from both proteins and small molecules to dis
play a relatively small set of functional groups often used in protein-RNA
recognition. Several studies have shown that the tethering of multiple bind
ing modules can enhance RNA-binding affinity and specificity, a strategy al
so commonly used in DNA recognition.