Self-assembly of large and small molecules into hierarchically ordered sacs and membranes

Science. 2008 Mar 28;319(5871):1812-6. doi: 10.1126/science.1154586.

Abstract

We report here the self-assembly of macroscopic sacs and membranes at the interface between two aqueous solutions, one containing a megadalton polymer and the other, small self-assembling molecules bearing opposite charge. The resulting structures have a highly ordered architecture in which nanofiber bundles align and reorient by nearly 90 degrees as the membrane grows. The formation of a diffusion barrier upon contact between the two liquids prevents their chaotic mixing. We hypothesize that growth of the membrane is then driven by a dynamic synergy between osmotic pressure of ions and static self-assembly. These robust, self-sealing macroscopic structures offer opportunities in many areas, including the formation of privileged environments for cells, immune barriers, new biological assays, and self-assembly of ordered thick membranes for diverse applications.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Cell Differentiation
  • Cell Survival
  • Chondrocytes / cytology
  • Diffusion
  • Elasticity
  • Humans
  • Hyaluronic Acid / chemistry*
  • Membranes, Artificial*
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / physiology
  • Microscopy, Electron
  • Nanostructures / chemistry
  • Osmotic Pressure
  • Peptides / chemistry*
  • Permeability
  • Polymers / chemistry*
  • Static Electricity
  • Transforming Growth Factor beta1 / chemistry

Substances

  • Membranes, Artificial
  • Peptides
  • Polymers
  • Transforming Growth Factor beta1
  • Hyaluronic Acid