4.6 Article

Assembly of chemically modified protein nanocages into 3D materials for the adsorption of uremic toxins

Journal

JOURNAL OF MATERIALS CHEMISTRY B
Volume 11, Issue 1, Pages 55-60

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2tb02386e

Keywords

-

Funding

  1. Liebig Scholarship
  2. Deutsche Forschungsgemeinschaft (DFG)
  3. Cluster of Excellence CUI: Advanced Imaging of Matter of the Deutsche Forschungsgemeinschaft (DFG)
  4. DFG research training group Nanohybrid
  5. [401323995]
  6. [390715994]
  7. [413227073]
  8. [GRK 2536]

Ask authors/readers for more resources

This study demonstrates the potential of protein-based adsorbents for clearing uremic toxins, with enhanced adsorption capacity and maintained biocompatibility through functionalization.
Hemodialysis fails to remove protein-bound uremic toxins that are attributed with high cardiovascular risk. Application of adsorption materials is a viable strategy, but suitable biocompatible adsorbents are still not available. Here, we demonstrate that adsorbents based on the bottom-up assembly of the intrinsically biocompatible protein cage ferritin are applicable for toxin adsorption. Due to the size-exclusion effect of its pores, only small molecules such as uremic toxins can enter the protein cage. Protein redesign techniques that target selectively the inner surface were used to introduce anchor sites for chemical modification. Porous crystalline adsorbents were fabricated by bottom-up assembly of the protein cage. Linkage of up to 96 phenylic or aliphatic molecules per container was verified by ESI-MS. Materials based on unmodified ferritin cages can already adsorb the uremic toxins. The adsorption capacity could be increased by about 50% through functionalization with hydrophobic molecules reaching 458 mu g g(-1) for indoxyl sulfate. The biohybrid materials show no contamination with endotoxins and do not activate blood platelets. These findings demonstrate the great potential of protein-based adsorbents for the clearance of uremic toxins: modifications enhance toxin adsorption without diminishing the biocompatibility of the final protein-based material.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available