The de novo design of polypeptide sequences with a three-dimensional s
tructure necessary for many biological functions is limited by the com
plex folding process, or 'protein folding problem'. This problem can b
e bypassed through constructing protein-like molecules with a 'built-i
n' device for intramolecular folding, that is, proteins of non-natural
chain architecture (template-assembled synthetic proteins, TASP). Top
ological templates have become a versatile tool for inducing and stabi
lizing secondary structures (protein loops, beta-turns, alpha-helices,
beta-sheets) and are widely adopted design elements for the construct
ion of protein-like molecules, exhibiting interesting structural and f
unctional properties.