TY - JOUR
T1 - Ice-Templated and Cross-Linked Amyloid Fibril Aerogel Scaffolds for Cell Growth
AU - Nyström, Gustav
AU - Fong, Wye Khay
AU - Mezzenga, Raffaele
N1 - Funding Information:
*E-mail: [email protected]. ORCID Wye-Khay Fong: 0000-0002-0437-9332 Raffaele Mezzenga: 0000-0002-5739-2610 Author Contributions The manuscript was written through contributions of all authors. All authors have given approval to the final version of the manuscript. Funding G.N. acknowledges funding from the Swiss National Science Foundation Ambizione Grant No. PZ00P2_168023/1. W.-K.F. is the recipient of a Victorian Postdoctoral Research Fellowship. Notes The authors declare no competing financial interest.
Funding Information:
We acknowledge support by the Scientific Center for Optical and Electron Microscopy of ETH Zurich (ScopeM). Dr. Tobias Schwartz is acknowledged for help with the Optical Microscopy setup. Dr. Tomaś de Wouters is acknowledged for supplying the HT29 and Caco2 cell lines.
Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/8/17
Y1 - 2017/8/17
N2 - Amyloid fibrils prepared from β-lactoglobulin were used to form freeze-dried and cross-linked aerogels. By varying the fibril concentration and freezing gradient, it was possible to control the pore structure and elastic modulus of the aerogels within one order of magnitude from ∼20 to ∼200 kPa. Using butane tetracarboxylic acid as cross-linker, these aerogels maintained their monolithic shape under aqueous conditions, displaying elastic behavior and a modulus in the range of ∼4-40 kPa. When explored as scaffolds for cell growth, the amyloid fibril aerogels demonstrated biocompatibility and led to the successful penetration and permeation of two epithelial cell lines (Caco-2 and HT29) throughout the scaffold. These soft, elastic, and water-stable biomaterials expand the scope of amyloid fibril aerogels, making them suitable for wet-state applications such as heterogeneous catalysis, purification membranes, and 3D matrices for cell growth.
AB - Amyloid fibrils prepared from β-lactoglobulin were used to form freeze-dried and cross-linked aerogels. By varying the fibril concentration and freezing gradient, it was possible to control the pore structure and elastic modulus of the aerogels within one order of magnitude from ∼20 to ∼200 kPa. Using butane tetracarboxylic acid as cross-linker, these aerogels maintained their monolithic shape under aqueous conditions, displaying elastic behavior and a modulus in the range of ∼4-40 kPa. When explored as scaffolds for cell growth, the amyloid fibril aerogels demonstrated biocompatibility and led to the successful penetration and permeation of two epithelial cell lines (Caco-2 and HT29) throughout the scaffold. These soft, elastic, and water-stable biomaterials expand the scope of amyloid fibril aerogels, making them suitable for wet-state applications such as heterogeneous catalysis, purification membranes, and 3D matrices for cell growth.
UR - https://www.scopus.com/pages/publications/85029218349
U2 - 10.1021/acs.biomac.7b00792
DO - 10.1021/acs.biomac.7b00792
M3 - Article
C2 - 28817771
AN - SCOPUS:85029218349
SN - 1525-7797
VL - 18
SP - 2858
EP - 2865
JO - Biomacromolecules
JF - Biomacromolecules
IS - 9
ER -