| Home > Publications database > Facially Amphipathic Glycopolymers Inhibit Ice Recrystallization > print |
| 001 | 845526 | ||
| 005 | 20210129233453.0 | ||
| 024 | 7 | _ | |a 10.1021/jacs.8b02066 |2 doi |
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| 100 | 1 | _ | |a Graham, Ben |0 0000-0003-1313-6874 |b 0 |
| 245 | _ | _ | |a Facially Amphipathic Glycopolymers Inhibit Ice Recrystallization |
| 260 | _ | _ | |a Washington, DC |c 2018 |b American Chemical Society |
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| 520 | _ | _ | |a Antifreeze glycoproteins (AFGPs) from polar fish are the most potent ice recrystallization (growth) inhibitors known, and synthetic mimics are required for low-temperature applications such as cell cryopreservation. Here we introduce facially amphipathic glycopolymers that mimic the three-dimensional structure of AFGPs. Glycopolymers featuring segregated hydrophilic and hydrophobic faces were prepared by ring-opening metathesis polymerization, and their rigid conformation was confirmed by small-angle neutron scattering. Ice recrystallization inhibition (IRI) activity was reduced when a hydrophilic oxo-ether was installed on the glycan-opposing face, but significant activity was restored by incorporating a hydrophobic dimethylfulvene residue. This biomimetic strategy demonstrates that segregated domains of distinct hydrophilicity/hydrophobicity are a crucial motif to introduce IRI activity, which increases our understanding of the complex ice crystal inhibition processes. |
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| 700 | 1 | _ | |a Gibson, Matthew I. |0 0000-0002-8297-1278 |b 4 |e Corresponding author |
| 773 | _ | _ | |a 10.1021/jacs.8b02066 |g Vol. 140, no. 17, p. 5682 - 5685 |0 PERI:(DE-600)1472210-0 |n 17 |p 5682 - 5685 |t Journal of the American Chemical Society |v 140 |y 2018 |x 1520-5126 |
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