RNA molecules were selected from a random sequence library for their a
bility to bind to an RNA stem-loop target. Oligonucleotides with exten
sive Watson-Crick complementarity to the RNA ligand were selected agai
nst by inclusion of a blocking oligodeoxynucleotide in the binding pha
se of the selection protocol. After 18 generations of SELEX (systemati
c evolution of ligands by exponential enrichment) a single RNA family
was predominant in the binding population. The winning aptamer RNA bou
nd the target RNA with an apparent K-d = 70 nM. Structural mapping and
Fe(II)-EDTA protection indicated that the target RNA interacted with
small unpaired loops in the aptamer structure. (C) 1997 Elsevier Scien
ce Ltd.