Large protein-based micellar aggegrates (see figure) are reversibly formed
upon self-assembly of the amphiphilic diblock copolymer-based on elastin-mi
metic peptide sequences-biosynthesized here. The biocompatibility, high rec
ombinant protein yields, physiological stability, and tunable responsive pr
operties of these polymers make them attractive candi- dates for controlled
delivery and release applications.