Rationally designed protein cross-linked hydrogel for bone regeneration via synergistic release of magnesium and zinc ions

Biomaterials. 2021 Jul:274:120895. doi: 10.1016/j.biomaterials.2021.120895. Epub 2021 May 12.

Abstract

The development of recombinant protein cross-linked injectable hydrogels with good mechanical strength and effective drug loading capacity for bone regeneration is extremely attractive and rarely reported. Here, we report the fabrication of a smart hydrogel delivery system by incorporating a rationally designed T4 lysozyme mutant (T4M) to mediate the localized delivery and synergistic release of Mg2+ and Zn2+ for bone repair. Apart from its intrinsic antibacterial properties, T4M bears abundant free amine groups on its surface to function as effective covalent crosslinkers to strengthen the hydrogel network as well as exhibits specific binding affinity to multivalent cations such as Zn2+. Moreover, the integrin receptor-binding Arg-Gly-Asp (RGD) sequence was introduced onto the C-terminus of T4 lysozyme to improve its cellular affinity and further facilitate rapid tissue regeneration. The final composite hydrogel displays excellent injectability, improved mechanical properties, antibacterial activity, and unique bioactivities. The effective loading of Mg2+/Zn2+ in the hydrogels could mediate the sequential and sustained release of Mg2+ and Zn2+, thereby resulting in synergistic enhancement on bone regeneration through modulation of the MAPK signaling pathway. We believe that the strategy proposed in this paper opens up a new route for developing protein cross-linked smart delivery systems for tissue regeneration.

Keywords: Bone-tissue engineering; Protein crosslinker; Protein engineering; Smart delivery system; Synergistic effect of bioactive ions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bone Regeneration
  • Hydrogels*
  • Ions
  • Magnesium*
  • Zinc

Substances

  • Hydrogels
  • Ions
  • Magnesium
  • Zinc