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Dopamine Self-Polymerization as a Simple and Powerful Tool to Modulate the Viscoelastic Mechanical Properties of Peptide-Based Gels

  1. Author:
    Fichman, Galit
    Schneider,Joel
  2. Author Address

    NCI, Biol Chem Lab, NIH, Frederick, MD 21702 USA.
    1. Year: 2021
    2. Date: Mar 4
  1. Journal: Molecules
  2. MDPI,
    1. 26
    2. 5
  3. Type of Article: Article
  4. Article Number: ARTN 1363
  5. ISSN: 1420-3049
  1. Abstract:

    Dopamine is a small versatile molecule used for various biotechnological and biomedical applications. This neurotransmitter, in addition to its biological role, can undergo oxidative self-polymerization to yield polydopamine, a robust universal coating material. Herein, we harness dopamine self-polymerization to modulate the viscoelastic mechanical properties of peptide-based gels, expanding their ever-growing application potential. By combining rapid peptide assembly with slower dopamine auto-polymerization, a double network gel is formed, where the fibrillar peptide gel network serves as a scaffold for polydopamine deposition, allowing polydopamine to interpenetrate the gel network as well as establishing crosslinks within the matrix. We have shown that triggering the assembly of a lysine-rich peptide gelator in the presence of dopamine can increase the mechanical rigidity of the resultant gel by a factor of 90 in some cases, while retaining the gel's shear thin-recovery behavior. We further investigate how factors such as polymerization time, dopamine concentration and peptide concentration alter the mechanical properties of the resultant gel. The hybrid peptide-dopamine gel systems were characterized using rheological measurements, circular dichroism spectroscopy and transmission electron microscopy. Overall, triggering peptide gelation in the presence of dopamine represents a simple yet powerful approach to modulate the viscoelastic mechanical properties of peptide-based gels.

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External Sources

  1. DOI: 10.3390/molecules26051363
  2. PMID: 33806346
  3. PMCID: PMC7961423
  4. WOS: 000628406700001

Library Notes

  1. Open Access Publication
  2. Fiscal Year: FY2020-2021
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