TY - CHAP
T1 - The Supramolecular Organization of a Peptide-Based Nanocarrier at High Molecular Detail
AU - Rad-Malekshahi, Mazda
AU - Visscher, Koen M.
AU - Rodrigues, João P.G.L.M.
AU - De Vries, Renko
AU - Hennink, Wim E.
AU - Baldus, Marc
AU - Bonvin, Alexandre M.J.J.
AU - Mastrobattista, Enrico
AU - Weingarth, Markus
PY - 2015/6/24
Y1 - 2015/6/24
N2 - Nanovesicles self-assembled from amphiphilic peptides are promising candidates for applications in drug delivery. However, complete high-resolution data on the local and supramolecular organization of such materials has been elusive thus far, which is a substantial obstacle to their rational design. In the absence of precise information, nanovesicles built of amphiphilic “lipid-like” peptides are generally assumed to resemble liposomes that are organized from bilayers of peptides with a tail-to-tail ordering. Using the nanocarrier formed by the amphiphilic self-assembling peptide 2 (SA2 peptide) as an example, we derive the local and global organization of a multimega-Dalton peptide-based nanocarrier at high molecular detail and at close-to physiological conditions. By integrating a multitude of experimental techniques (solid-state NMR, AFM, SLS, DLS, FT-IR, CD) with large- and multiscale MD simulations, we show that SA2 nanocarriers are built of interdigitated antiparallel β-sheets, which bear little res...
AB - Nanovesicles self-assembled from amphiphilic peptides are promising candidates for applications in drug delivery. However, complete high-resolution data on the local and supramolecular organization of such materials has been elusive thus far, which is a substantial obstacle to their rational design. In the absence of precise information, nanovesicles built of amphiphilic “lipid-like” peptides are generally assumed to resemble liposomes that are organized from bilayers of peptides with a tail-to-tail ordering. Using the nanocarrier formed by the amphiphilic self-assembling peptide 2 (SA2 peptide) as an example, we derive the local and global organization of a multimega-Dalton peptide-based nanocarrier at high molecular detail and at close-to physiological conditions. By integrating a multitude of experimental techniques (solid-state NMR, AFM, SLS, DLS, FT-IR, CD) with large- and multiscale MD simulations, we show that SA2 nanocarriers are built of interdigitated antiparallel β-sheets, which bear little res...
U2 - 10.1021/jacs.5b02919
DO - 10.1021/jacs.5b02919
M3 - Chapter
C2 - 26022089
SN - 0002-7863
VL - 137
T3 - Journal of the American Chemical Society
SP - 7775
EP - 7784
BT - Journal of the American Chemical Society
PB - American Chemical Society
ER -