A Biomimetic Escape Strategy for Cytoplasm Invasion by Synthetic Particles

Angew Chem Int Ed Engl. 2017 Oct 23;56(44):13736-13740. doi: 10.1002/anie.201707769. Epub 2017 Oct 2.

Abstract

The translocation of nanomaterials or complex delivery systems into the cytosol is a major challenge in nanobiotechnology. After receptor-mediated endocytosis, most nanomaterials are sequestered and undergo degradation, therapy inactivation, or exocytosis. Herein we explore a novel surface particle coating made of adsorbed carbon nanotubes that provides coated materials with new properties that reproduce the viral cell-invasive mechanisms, namely, receptor-mediated endocytosis, endolysosomal escape, and cytosolic particle release preserving cell viability. This novel biomimetic coating design will enable the intracytoplasmic delivery of many different functional materials endowed with therapeutic, magnetic, optical, or catalytic functionalities, thus opening the door to a wide array of chemical and physical processes within the cytosolic or nuclear domains, and supporting new developments in the biotechnological, pharmaceutical, and biomedical industries.

Keywords: biomimetic coatings; carbon nanotubes; cell recognition; cytoplasmic invasion; endocytosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomimetic Materials / chemistry
  • Biomimetic Materials / metabolism*
  • Biomimetics
  • Cell Survival
  • Coated Materials, Biocompatible / chemistry
  • Coated Materials, Biocompatible / metabolism*
  • Cytoplasm / metabolism*
  • Endocytosis*
  • HeLa Cells
  • Humans
  • Nanoparticles / chemistry
  • Nanoparticles / metabolism*
  • Nanotubes, Carbon / chemistry
  • Silicon Dioxide / chemistry
  • Silicon Dioxide / metabolism*
  • Surface Properties

Substances

  • Coated Materials, Biocompatible
  • Nanotubes, Carbon
  • Silicon Dioxide