Dual mechanism β-amino acid polymers promoting cell adhesion
Qi Chen,
Donghui Zhang,
Wenjing Zhang,
Haodong Zhang,
Jingcheng Zou,
Mingjiao Chen,
Jin Li,
Yuan Yuan and
Runhui Liu ()
Additional contact information
Qi Chen: East China University of Science and Technology
Donghui Zhang: East China University of Science and Technology
Wenjing Zhang: East China University of Science and Technology
Haodong Zhang: East China University of Science and Technology
Jingcheng Zou: East China University of Science and Technology
Mingjiao Chen: Shanghai Jiao Tong University School of Medicine
Jin Li: Shanghai Jiao Tong University School of Medicine
Yuan Yuan: East China University of Science and Technology
Runhui Liu: East China University of Science and Technology
Nature Communications, 2021, vol. 12, issue 1, 1-13
Abstract:
Abstract Cell adhesion has tremendous impact on the function of culture platforms and implants. Cell-adhesive proteins and peptides have been extensively used for decades to promote cell adhesion, however, their application suffers from their easy enzymatic degradation, difficulty in large-scale preparation and expensiveness. To develop the next-generation cell-adhesive materials, we mimic the cell adhesion functions and mechanisms of RGD and KRSR peptides and design cell-adhesive cationic-hydrophobic amphiphilic β-amino acid polymers that are stable upon proteolysis and easily prepared in large scale at low cost. The optimal polymer strongly promotes cell adhesion, using preosteoblast cell as a model, by following dual mechanisms that are independent of sequence and chirality of the statistic copolymer. Our strategy opens avenues in designing the next-generation cell-adhesive materials and may guide future studies and applications.
Date: 2021
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-020-20858-x
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DOI: 10.1038/s41467-020-20858-x
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