Mechanotransductive surfaces for reversible biocatalysis activation

Nat Mater. 2009 Sep;8(9):731-5. doi: 10.1038/nmat2504. Epub 2009 Aug 9.

Abstract

Fibronectin, like other proteins involved in mechanotransduction, has the ability to exhibit recognition sites under mechanical stretch. Such cryptic sites are buried inside the protein structure in the native fold and become exposed under an applied force, thereby activating specific signalling pathways. Here, we report the design of new active polymeric nanoassembled surfaces that show some similarities to these cryptic sites. These nanoassemblies consist of a first polyelectrolyte multilayer stratum loaded with enzymes and capped with a second polyelectrolyte multilayer acting as a mechanically sensitive nanobarrier. The biocatalytic activity of the film is switched on/off reversibly by mechanical stretching, which exposes enzymes through the capping barrier, similarly to mechanisms involved in proteins during mechanotransduction. This first example of a new class of biologically inspired surfaces should have great potential in the design of various devices aimed to trigger and modulate chemical reactions by mechanical action with applications in the field of microfluidic devices or mechanically controlled biopatches for example.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adsorption
  • Alkaline Phosphatase / chemistry
  • Alkaline Phosphatase / metabolism
  • Biocatalysis*
  • Biomechanical Phenomena
  • Diphosphates / chemistry
  • Electrolytes
  • Enzyme Activation*
  • Fluorescein / chemistry
  • Fluorescein / metabolism
  • Hyaluronic Acid / chemistry
  • Oxidation-Reduction
  • Polylysine / chemistry
  • Stress, Mechanical*
  • Surface Properties

Substances

  • Diphosphates
  • Electrolytes
  • Polylysine
  • Hyaluronic Acid
  • Alkaline Phosphatase
  • Fluorescein