Peptide-ba
sed ve
sicular
structure
s have been the focu
s of re
search in the pa
st decade for their potential applicationa
s drug delivery agent
s. We here report the
self-a
ssembly of amphiphilic dipeptide
s containing conformation-con
straining
s/gifchar
s/alpha.gif" BORDER=0>,
s/gifchar
s/beta2.gif" BORDER=0 ALIGN="middle">-dehydrophenylalanine into nanove
sicle
s. The ve
sicle
s can encap
sulate
small drug molecule
s such a
s riboflavinand vitamin B
12, bioactive peptide
s, and
small protein molecule
s. The nanove
sicle
s are re
si
stant to treatment of anon
specific protea
se, proteina
se K, and are
stable at low concentration
s of monovalent and divalent cation
s. Theve
sicle
s are effectively taken up by actively growing cell
s in culture and
show no ob
servable cytopathic effect
s. The
sepeptide-ba
sed nano
structure
s can be con
sidered a
s model
s for further development a
s delivery agent
s for differentbiomolecule
s.