Fabrication of multifunctional metal-organic frameworks nanoparticles via layer-by-layer self-assembly to efficiently discover PSD95-nNOS uncouplers for stroke treatment

J Nanobiotechnology. 2022 Aug 13;20(1):379. doi: 10.1186/s12951-022-01583-7.

Abstract

Background: Disruption of the postsynaptic density protein-95 (PSD95)-neuronal nitric oxide synthase (nNOS) coupling is an effective way to treat ischemic stroke, however, it still faces some challenges, especially lack of satisfactory PSD95-nNOS uncouplers and the efficient high throughput screening model to discover them.

Results: Herein, the multifunctional metal-organic framework (MMOF) nanoparticles as a new screening system were innovatively fabricated via layer-by-layer self-assembly in which His-tagged nNOS was selectively immobilized on the surface of magnetic MOF, and then PSD95 with green fluorescent protein (GFP-PSD95) was specifically bound on it. It was found that MMOF nanoparticles not only exhibited the superior performances including the high loading efficiency, reusability, and anti-interference ability, but also possessed the good fluorescent sensitivity to detect the coupled GFP-PSD95. After MMOF nanoparticles interacted with the uncouplers, they would be rapidly separated from uncoupled GFP-PSD95 by magnet, and the fluorescent intensities could be determined to assay the uncoupling efficiency at high throughput level.

Conclusions: In conclusion, MMOF nanoparticles were successfully fabricated and applied to screen the natural actives as potential PSD95-nNOS uncouplers. Taken together, our newly developed method provided a new material as a platform for efficiently discovering PSD95-nNOS uncouplers for stoke treatment.

Keywords: Coordinative immobilization; Fluorescent sensitivity; PSD95-nNOS uncouplers; multifunctional nanoparticles.

MeSH terms

  • Animals
  • Disks Large Homolog 4 Protein / metabolism
  • Metal-Organic Frameworks*
  • Nanoparticles*
  • Nitric Oxide Synthase Type I / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Stroke*
  • Transcription Factors

Substances

  • Disks Large Homolog 4 Protein
  • Metal-Organic Frameworks
  • Transcription Factors
  • Nitric Oxide Synthase Type I