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The Design of a Participatory Peptide Nucleic Acid Duplex Crosslinker to Enhance the Stiffness of Self-Assembled Peptide Gels

  1. Author:
    Sarkar,Srijani
    Anderson,Caleb
    Schneider,Joel
  2. Author Address

    National Cancer Institute Center for Cancer Research, Chemical Biology Laboratory, 1050 Boyles Street, Building 376, Room 104, Chemical Biology Laboratory, 21702-1178, Frederick, UNITED STATES., National Cancer Institute at Frederick, Chemical Biology Laboratory, 1050 Boyles Street, Building 376, Room 104, Chemical Biology Laboratory, 21702, Frederick, UNITED STATES., National Cancer Institute at Frederick: NCI at Frederick, 1050 Boyles Street, 21702, Frederick, UNITED STATES.,
    1. Year: 2023
    2. Date: Dec 06
    3. Epub Date: 2023 12 06
  1. Journal: Angewandte Chemie (International ed. in English)
    1. Pages: e202313507
  2. Type of Article: Article
  3. Article Number: e202313507
  1. Abstract:

    Herein, peptide nucleic acids (PNAs) are employed in the design of a participatory duplex PNA-peptide crosslinking agent. Biophysical and mechanical studies show that crosslinkers present during peptide assembly leading to hydrogelation participate in the formation of fibrils while simultaneously installing crosslinks into the higher-order network that constitutes the peptide gel. The addition of 2 mol% crosslinker into the assembling system results in a ~100% increase in mechanical stiffness without affecting the rate of peptide assembly or the local morphology of fibrils within the gel network. Stiffness enhancement is realized by only affecting change in the elastic component of the viscoelastic gel. A synthesis of the PNA-peptide duplex crosslinkers is provided that allows facile variation in peptide composition and addresses the notorious hydrophobic content of PNAs. This crosslinking system represents a new tool for modulating the mechanical properties of peptide-based hydrogels. © 2023 Wiley-VCH GmbH.

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External Sources

  1. DOI: 10.1002/anie.202313507
  2. PMID: 38057633

Library Notes

  1. Fiscal Year: FY2023-2024
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