Stretch-Induced Helical Conformations in Poly(l -lysine)/Hyaluronic Acid Multilayers
Author(s) -
Sarah Zahouani,
Alain Chaumont,
Bernard Senger,
Fouzia Boulmedais,
Pierre Schaaf,
Loı̈c Jierry,
Philippe Lavall�e
Publication year - 2015
Publication title -
acs applied materials and interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.535
H-Index - 228
eISSN - 1944-8252
pISSN - 1944-8244
DOI - 10.1021/acsami.5b08302
Subject(s) - lysine , helix (gastropod) , crystallography , materials science , molecular dynamics , protein secondary structure , side chain , biophysics , polymer , amino acid , chemistry , biochemistry , computational chemistry , biology , ecology , snail , composite material
We investigate the effect of stretching on the secondary structure of cross-linked poly(l-lysine)/hyaluronic acid (PLL/HA) multilayers. We show that stretching these films induces changes in the secondary structure of PLL chains. Our results suggest that not only α- but also 310-helices might form in the film under stretching. Such 310-helices have never been observed for PLL so far. These changes of the secondary structure of PLL are reversible, i.e., when returning to the nonstretched state one recovers the initial film structure. Using molecular dynamics simulations of chains composed of 20 l-lysine residues (PLL20), we find that these chains never adopt a helical conformation in water. In contrast, when the end-to-end distance of the chains is restrained to values smaller than the mean end-to-end distance of free chains, a distance domain rarely explored by the free chains, helical conformations become accessible. Moreover, the formation of not only α- but also 310-helices is predicted by the simulations. These results suggest that the change of the end-to-end distance of PLL chains in the stretched film is at the origin of the helix formation.
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