2017
DOI: 10.1038/srep40913
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Sialic Acid-Responsive Polymeric Interface Material: From Molecular Recognition to Macroscopic Property Switching

Abstract: Biological systems that utilize multiple weak non-covalent interactions and hierarchical assemblies to achieve various bio-functions bring much inspiration for the design of artificial biomaterials. However, it remains a big challenge to correlate underlying biomolecule interactions with macroscopic level of materials, for example, recognizing such weak interaction, further transforming it into regulating material’s macroscopic property and contributing to some new bio-applications. Here we designed a novel sm… Show more

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Cited by 8 publications
(2 citation statements)
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References 60 publications
(66 reference statements)
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“…Furthermore, in order to better mimic the structure of oligosaccharides involved in the SA recognition process, we recently improved the material design and focused on disaccharide to prepare a glycopolymeric interface material based on polyacrylamide grafted with lactose (denoted as PAM- g -lactose), with the expectation to present more outstanding target recognition and binding capability [ 80 ]. After similar screening steps, lactose came to the fore and specifically recognized SA.…”
Section: Bio-inspired Materials For Sa Derivatives Separation/enrimentioning
confidence: 99%
“…Furthermore, in order to better mimic the structure of oligosaccharides involved in the SA recognition process, we recently improved the material design and focused on disaccharide to prepare a glycopolymeric interface material based on polyacrylamide grafted with lactose (denoted as PAM- g -lactose), with the expectation to present more outstanding target recognition and binding capability [ 80 ]. After similar screening steps, lactose came to the fore and specifically recognized SA.…”
Section: Bio-inspired Materials For Sa Derivatives Separation/enrimentioning
confidence: 99%
“…For instance, catechol-functionalized polymers (i.e., chitosancatechol [20][21][22] , hyaluronic acid-catechol 23,24 , and alginate-catechol 25 ) exhibit significant enhancements of tissue adhesions compared to unmodified polymers. PBA conjugation also provides adhesive properties by boronate ester formation with glycoproteins, peptidoglycan, and polysaccharides [26][27][28][29][30][31][32] . Furthermore, CB-containing hydrogels are long-lasting under physiological conditions compared with hydrogels without CB.…”
mentioning
confidence: 99%