4.8 Article

A self-assembly pathway to aligned monodomain gels

Journal

NATURE MATERIALS
Volume 9, Issue 7, Pages 594-601

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/NMAT2778

Keywords

-

Funding

  1. US Department of Energy-Basic Energy Sciences [DE-FG02-00ER45810, DE-FG02-08ER46539]
  2. National Institutes of Health [5-R01-EB003806, 5-R01-DE015920, 5-P50-NS054287]
  3. National Science Foundation [DMR-0605427]
  4. Department of Homeland Security Fellowship
  5. Non-Equilibrium Energy Research Center (NERC)
  6. DOE-BES [DE-SC0000989]
  7. Northwestern University
  8. Ben Gurion University of Negev, Israel
  9. NSF-NSEC
  10. NSF-MRSEC [DMR-0520513]
  11. Keck Foundation
  12. State of Illinois
  13. E. I. DuPont de Nemours
  14. The Dow Chemical Company
  15. US National Science Foundation [DMR-9304725]
  16. State of Illinois through the Department of Commerce and the Board of Higher Education [IBHE HECA NWU 96]
  17. US Department of Energy-Office of Basic Energy Sciences [W-31-109-Eng-38, DE-AC02-06CH11357]
  18. National Institutes of Health, National Center for Research Resources [RR007707]
  19. Generalitat de Catalunya
  20. Division Of Materials Research
  21. Direct For Mathematical & Physical Scien [1006713] Funding Source: National Science Foundation

Ask authors/readers for more resources

Aggregates of charged amphiphilic molecules have been found to access a structure at elevated temperature that templates alignment of supramolecular fibrils over macroscopic scales. The thermal pathway leads to a lamellar plaque structure with fibrous texture that breaks on cooling into large arrays of aligned nanoscale fibres and forms a strongly birefringent liquid. By manually dragging this liquid crystal from a pipette onto salty media, it is possible to extend this alignment over centimetres in noodle-shaped viscoelastic strings. Using this approach, the solution of supramolecular filaments can be mixed with cells at physiological temperatures to form monodomain gels of aligned cells and filaments. The nature of the self-assembly process and its biocompatibility would allow formation of cellular wires in situ that have any length and customized peptide compositions for use in biological applications.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available