|
 |
 |

NEWS
INDEX
Archives
2004
August
Self-assembly generates more versatile
scaffolds for crystal growth
James
E. Kloeppel, Physical Sciences Editor
217-244-1073; kloeppel@uiuc.edu
8/31/04
 |
Click
photo to enlarge |
| Photo
by Kwame Ross |
| “By
investigating the fundamental design rules for the control
of self-assembled supramolecular structures, we can now organize
large functional molecules into nanoscopic arrays,”
said Gerard Wong, a professor of materials science and engineering
and of physics at the University of Illinois. |
|
CHAMPAIGN,
Ill. — Self-organizing synthetic molecules originally used for
gene therapy may have applications as templates and scaffolds for the
production of inorganic materials. Using electrostatic interactions
between oppositely charged molecules as the binding force, scientists
are learning how to organize these synthetic molecules into more versatile
complexes with large and controllable pore sizes.
“By investigating the fundamental design rules for the control
of self-assembled supramolecular structures, we can now organize large
functional molecules into nanoscopic arrays,” said Gerard Wong,
a professor of materials science
and engineering and of physics
at the University of Illinois. Wong and his colleagues report their
latest experimental results in the September issue of the journal Nature
Materials.
“We showed that the self-assembly of charged membranes and oppositely
charged polymers into structures can be understood in terms of some
simple rules,” said Wong, senior author of the paper. “We
then applied those rules and demonstrated that we could organize molecules
into regular arrays with pore sizes ten times larger than in previous
DNA-membrane complexes.”
Early self-assembled DNA-membrane structures consisted of periodic stacks
of alternating layers of negatively charged DNA “rods” and
positively charged lipid membranes. The pores between the DNA rods could
be used to package individual ions, which can in turn be crystallized.
This work was published last year by Wong’s group, and was featured
as a “Chemistry Highlight of 2003” by Chemical & Engineering
News.
But generalizing this idea to larger pores was difficult. In previous
work, Wong and colleagues showed that actin, a protein found in muscle
cells, also reacts with lipid membranes to create ordered structures.
The actin-membrane assemblies, however, consisted of the membrane sandwiched
between layers of actin, with little room to house or organize other
molecules.
In the latest work, the researchers substituted a rod-shaped virus for
the DNA. While having a diameter close to that of actin, the virus has
a charge density comparable to DNA. The resulting virus-membrane complexes
have pore sizes about 10 times larger than the DNA-membrane complexes,
and can be used to hold and organize large functional molecules.
“Even though these supramolecular systems were originally designed
for gene therapy, we’ve shown that they can be used as templates
for organizing other molecules,” Wong said. “An example
would be the biomineralization of inorganic nanocrystals, in a way analogous
to bone formation.”
To produce bone, nature uses organic molecules to organize inorganic
components that become mineralized through additional chemical reactions.
Scientists want to create synthetic molecules that work as nanostructured
scaffolds of biomolecules and perform tasks ranging from non-viral gene
therapy to biomolecular templating and nanofabrication.
“Ultimately, we would like to have designer molecules that do
exactly what we want,” Wong said. “Right now we are still
elucidating the rules for making these scaffolds and their interactions
with inorganic components. It will take some time to move from fundamental
science to supramolecular engineering.”
Co-authors of the paper with Wong are Illinois graduate students Lihua
Yang, Hongjun Liang, Thomas Angelini, John Butler and Robert Coridan;
and Brown University physics professor Jay Tang. The work was funded
by the U.S. Department of Energy and the National Science Foundation.
|
 |
 |
|