Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/95063
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dc.contributorDepartment of Biomedical Engineeringen_US
dc.creatorHe, Wen_US
dc.creatorBai, Jen_US
dc.creatorChen, Xen_US
dc.creatorSuo, Den_US
dc.creatorWang, Sen_US
dc.creatorGuo, Qen_US
dc.creatorYin, Wen_US
dc.creatorGeng, Den_US
dc.creatorWang, Men_US
dc.creatorPan, Gen_US
dc.creatorZhao, Xen_US
dc.creatorLi, Ben_US
dc.date.accessioned2022-09-13T03:37:00Z-
dc.date.available2022-09-13T03:37:00Z-
dc.identifier.issn0027-8424en_US
dc.identifier.urihttp://hdl.handle.net/10397/95063-
dc.language.isoenen_US
dc.publisherNational Academy of Sciencesen_US
dc.rightsCopyright © 2022 the Author(s). Published by PNAS.en_US
dc.rightsThis article is distributed under Creative Commons Attribution-NonCommercialNoDerivatives License 4.0 (CC BY-NC-ND)(https://creativecommons.org/licenses/by-nc-nd/4.0/).en_US
dc.rightsThe following publication He, W., Bai, J., Chen, X., Suo, D., Wang, S., Guo, Q., ... & Li, B. (2022). Reversible dougong structured receptor–ligand recognition for building dynamic extracellular matrix mimics. Proceedings of the National Academy of Sciences, 119(8), e2117221119 is available at https://doi.org/10.1073/pnas.2117221119.en_US
dc.subjectBiomimicryen_US
dc.subjectCell regulationen_US
dc.subjectDynamic biomaterial designen_US
dc.subjectNatural receptor–ligand interactionen_US
dc.subjectTissue repairen_US
dc.titleReversible dougong structured receptor–ligand recognition for building dynamic extracellular matrix mimicsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.volume119en_US
dc.identifier.issue8en_US
dc.identifier.doi10.1073/pnas.2117221119en_US
dcterms.abstractDynamic biomaterials excel at recapitulating the reversible interlocking and remoldable structure of the extracellular matrix (ECM), particularly in manipulating cell behaviors and adapting to tissue morphogenesis. While strategies based on dynamic chemistries have been extensively studied for ECM-mimicking dynamic biomaterials, biocompatible molecular means with biogenicity are still rare. Here, we report a nature-derived strategy for fabrication of dynamic biointerface as well as a three-dimensional (3D) hydrogel structure based on reversible receptor–ligand interaction between the glycopeptide antibiotic vancomycin and dipeptide D-Ala-D-Ala. We demonstrate the reversible regulation of multiple cell types with the dynamic biointerface and successfully implement the dynamic hydrogel as a functional antibacterial 3D scaffold to treat tissue repair. In view of the biogenicity and high applicability, this nature-derived reversible molecular strategy will bring opportunities for malleable biomaterial design with great potential in biomedicine.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationProceedings of the National Academy of Sciences of the United States of America, 22 Feb. 2022, v. 119, no. 8, e2117221119en_US
dcterms.isPartOfProceedings of the National Academy of Sciences of the United States of Americaen_US
dcterms.issued2022-02-22-
dc.identifier.scopus2-s2.0-85124927045-
dc.identifier.pmid35181608-
dc.identifier.ros2021003444-
dc.identifier.eissn1091-6490en_US
dc.identifier.artne2117221119en_US
dc.description.validate202209 bchyen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberCDCF_2021-2022-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Key Research and Development Program of China Grants; National Natural Science Foundation of China Grants; the Innovation and Entrepreneurship Program of Jiangsu Province; “Six Talent Peaks” Program of Jiangsu Province Granten_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS68127225-
dc.description.oaCategoryCCen_US
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