Engineering proteins to bind small molecules presents a challenge as daunti
ng as drug discovery, for both hinge upon our understanding of receptor-lig
and molecular recognition. However, powerful techniques from combinatorial
molecular biology can be used to rapidly select artificial receptors. While
traditionally researchers have relied upon antibody technologies as a sour
ce of new binding proteins, the lipocalin scaffold has recently emerged as
an adaptable receptor for small molecule binding. 'Anticalins', engineered
lipocalin variants, offer some advantages over traditional antibody technol
ogy and illuminate features of molecular recognition between receptors and
small molecule ligands.