Nanolithographic control of the spatial organization of cellular adhesion receptors at the single-molecule level

Mark Schvartzman, Matteo Palma, Julia Sable, Justin Abramson, Xian Hu, Michael Sheetz, Shalom J. Wind

Research output: Contribution to journalArticle

135 Citations (Scopus)

Abstract

The ability to control the placement of individual molecules promises to enable a wide range of applications and is a key challenge in nanoscience and nanotechnology. Many biological interactions, in particular, are sensitive to the precise geometric arrangement of proteins. We have developed a technique which combines molecular-scale nanolithography with site-selective biochemistry to create biomimetic arrays of individual protein binding sites. The binding sites can be arranged in heterogeneous patterns of virtually any possible geometry with a nearly unlimited number of degrees of freedom. We have used these arrays to explore how the geometric organization of the extracellular matrix (ECM) binding ligand RGD (Arg-Gly-Asp) affects cell adhesion and spreading. Systematic variation of spacing, density, and cluster size of individual integrin binding sites was used to elicit different cell behavior. Cell spreading assays on arrays of different geometric arrangements revealed a dramatic increase in spreading efficiency when at least four liganded sites were spaced within 60 nm or less, with no dependence on global density. This points to the existence of a minimal matrix adhesion unit for fibronectin defined in space and stoichiometry. Developing an understanding of the ECM geometries that activate specific cellular functional complexes is a critical step toward controlling cell behavior. Potential practical applications range from new therapeutic treatments to the rational design of tissue scaffolds that can optimize healing without scarring. More broadly, spatial control at the single-molecule level can elucidate factors controlling individual molecular interactions and can enable synthesis of new systems based on molecular-scale architectures.

Original languageEnglish (US)
Pages (from-to)1306-1312
Number of pages7
JournalNano Letters
Volume11
Issue number3
DOIs
StatePublished - Mar 9 2011
Externally publishedYes

Fingerprint

Binding sites
adhesion
Adhesion
Binding Sites
Molecules
cells
Tissue Scaffolds
Nanoscience
Nanolithography
molecules
Biochemistry
Molecular interactions
Geometry
matrices
Cell adhesion
Biomimetics
proteins
Nanotechnology
Fibronectins
Integrins

Keywords

  • cell adhesion
  • integrin clustering
  • mechanobiology
  • nanobiology
  • Nanofabrication

ASJC Scopus subject areas

  • Condensed Matter Physics
  • Bioengineering
  • Chemistry(all)
  • Materials Science(all)
  • Mechanical Engineering

Cite this

Nanolithographic control of the spatial organization of cellular adhesion receptors at the single-molecule level. / Schvartzman, Mark; Palma, Matteo; Sable, Julia; Abramson, Justin; Hu, Xian; Sheetz, Michael; Wind, Shalom J.

In: Nano Letters, Vol. 11, No. 3, 09.03.2011, p. 1306-1312.

Research output: Contribution to journalArticle

Schvartzman, Mark ; Palma, Matteo ; Sable, Julia ; Abramson, Justin ; Hu, Xian ; Sheetz, Michael ; Wind, Shalom J. / Nanolithographic control of the spatial organization of cellular adhesion receptors at the single-molecule level. In: Nano Letters. 2011 ; Vol. 11, No. 3. pp. 1306-1312.
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