2022
DOI: 10.1039/d2nr03715g
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Ring -opening of polythiolactones to construct protein-imprinted nanospheres with high recognition and regulation capabilities

Abstract: Developing and preparing novel protein imprinted nanomaterials with high recognition ability remains challenging because it is difficult to controllably and orderly design functional groups and arrangement of functional groups of...

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Cited by 3 publications
(2 citation statements)
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“…The disappearance of the peak at 918 cm −1 in MS@PTL-g-PNIPAM provides strong evidence for the complete ammonolysis of the thiolactone side groups. [21] The characteristic element peaks of different nanospheres in the X-ray photoelectron spectra (XPS) also indicates that all modifications were in order and all nanospheres were prepared as expected (Figure 1d and Figure S12, Supporting Information). Furthermore, all nanospheres are thermally stable up to 200 °C (Figure S13, Supporting Information) and magnetic enough to meet the needs of magnetic separation (Figure S14, Supporting Information).…”
Section: Synthesis and Characterization Of Ms@ptl-g-pnipamsupporting
confidence: 58%
See 1 more Smart Citation
“…The disappearance of the peak at 918 cm −1 in MS@PTL-g-PNIPAM provides strong evidence for the complete ammonolysis of the thiolactone side groups. [21] The characteristic element peaks of different nanospheres in the X-ray photoelectron spectra (XPS) also indicates that all modifications were in order and all nanospheres were prepared as expected (Figure 1d and Figure S12, Supporting Information). Furthermore, all nanospheres are thermally stable up to 200 °C (Figure S13, Supporting Information) and magnetic enough to meet the needs of magnetic separation (Figure S14, Supporting Information).…”
Section: Synthesis and Characterization Of Ms@ptl-g-pnipamsupporting
confidence: 58%
“…Next, three selected amine ligands (i.e., ethanolamine, β‐alanine, 1‐(2‐aminoethyl) pyrrolidine) were used to open the ring of the thiolactone side groups to introduce abundant functional groups (hydroxyl, carboxyl, and pyrrolidine groups) for anchoring of template proteins in the imprinting polymerization because of the excellent hydrogen bonding and hydrophobic interactions between these functional groups and proteins according to our previous study. [ 21 ] The ring‐opening process meanwhile produced sufficient thiols for grafting of functional polymers (MS@PTL‐RP). Finally, a coumarin‐terminated temperature‐responsive functional polymer PNIPAM (Coumarin‐PNIPAM‐Br) was grafted onto the surface of MS@PTL‐RP to obtain MS@PTL‐g‐PNIPAM through a thiol‐bromine click reaction.…”
Section: Resultsmentioning
confidence: 99%