TY - JOUR
T1 - Design of synthetic collagens that assemble into supramolecular banded fibers as a functional biomaterial testbed
AU - Hu, Jinyuan
AU - Li, Junhui
AU - Jiang, Jennifer
AU - Wang, Lingling
AU - Roth, Jonathan
AU - McGuinness, Kenneth N.
AU - Baum, Jean
AU - Dai, Wei
AU - Sun, Yao
AU - Nanda, Vikas
AU - Xu, Fei
N1 - Funding Information:
We wish to thank the core imaging facilities at the School of Biotechnology, Jiangnan University, and Robert Wood Johnson Medical School, Rutgers University for help obtaining TEM images. This work was supported by the National Key R&D Program of China (No. 2018YFA0901600) and the National Natural Science Foundation of China (No. 22078129) to FX, National Institute of Health of US (No. R35- GM136431) to JB, NASA NAI 80NSSC18M0093 (VN), and National Natural Science Foundation of China (No. 82270963, No. 82061130222) and Foundation of SCST (No. 20XD1424000, 201409006400) to YS.
Funding Information:
We wish to thank the core imaging facilities at the School of Biotechnology, Jiangnan University, and Robert Wood Johnson Medical School, Rutgers University for help obtaining TEM images. This work was supported by the National Key R&D Program of China (No. 2018YFA0901600) and the National Natural Science Foundation of China (No. 22078129) to FX, National Institute of Health of US (No. R35- GM136431) to JB, NASA NAI 80NSSC18M0093 (VN), and National Natural Science Foundation of China (No. 82270963, No. 82061130222) and Foundation of SCST (No. 20XD1424000, 201409006400) to YS.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - Collagens are the most abundant proteins of the extracellular matrix, and the hierarchical folding and supramolecular assembly of collagens into banded fibers is essential for mediating cell-matrix interactions and tissue mechanics. Collagen extracted from animal tissues is a valuable commodity, but suffers from safety and purity issues, limiting its biomaterials applications. Synthetic collagen biomaterials could address these issues, but their construction requires molecular-level control of folding and supramolecular assembly into ordered banded fibers, comparable to those of natural collagens. Here, we show an innovative class of banded fiber-forming synthetic collagens that recapitulate the morphology and some biological properties of natural collagens. The synthetic collagens comprise a functional-driver module that is flanked by adhesive modules that effectively promote their supramolecular assembly. Multiscale simulations support a plausible molecular-level mechanism of supramolecular assembly, allowing precise design of banded fiber morphology. We also experimentally demonstrate that synthetic fibers stimulate osteoblast differentiation at levels comparable to natural collagen. This work thus deepens understanding of collagen biology and disease by providing a ready source of safe, functional biomaterials that bridge the current gap between the simplicity of peptide biophysical models and the complexity of in vivo animal systems.
AB - Collagens are the most abundant proteins of the extracellular matrix, and the hierarchical folding and supramolecular assembly of collagens into banded fibers is essential for mediating cell-matrix interactions and tissue mechanics. Collagen extracted from animal tissues is a valuable commodity, but suffers from safety and purity issues, limiting its biomaterials applications. Synthetic collagen biomaterials could address these issues, but their construction requires molecular-level control of folding and supramolecular assembly into ordered banded fibers, comparable to those of natural collagens. Here, we show an innovative class of banded fiber-forming synthetic collagens that recapitulate the morphology and some biological properties of natural collagens. The synthetic collagens comprise a functional-driver module that is flanked by adhesive modules that effectively promote their supramolecular assembly. Multiscale simulations support a plausible molecular-level mechanism of supramolecular assembly, allowing precise design of banded fiber morphology. We also experimentally demonstrate that synthetic fibers stimulate osteoblast differentiation at levels comparable to natural collagen. This work thus deepens understanding of collagen biology and disease by providing a ready source of safe, functional biomaterials that bridge the current gap between the simplicity of peptide biophysical models and the complexity of in vivo animal systems.
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U2 - 10.1038/s41467-022-34127-6
DO - 10.1038/s41467-022-34127-6
M3 - Article
C2 - 36351904
AN - SCOPUS:85141480319
SN - 2041-1723
VL - 13
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 6761
ER -