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David
A. Tirrell
Ross
McCollum-William H. Corcoran Professor and Professor of Chemistry
and Chemical Engineering
Chair, Division of Chemistry and Chemical Engineering
Research
in the Tirrell group combines organic, biological, and materials chemistry
to make new polymeric systems of controlled molecular and supramolecular
architectures. Two kinds of systems are under active investigation:
artificial proteins made by expression of artificial genes in microbial
cells, and flexible polymeric nanowires and nanotubes made by a membrane
templating approach. In each case, investigators are concerned not
only with architectural control but also with the functional properties
of the macromolecular system of interest.
Artificial proteins represent a new class of macromolecular materials
that bridge the gap that has traditionally separated natural polymers
from their synthetic counterparts. While synthetic polymers are interesting
and enormously important, their utility derives in large part from
their physical properties; chemists have yet to capture in synthetic
polymers the more subtle catalytic, informational, and transduction
properties of proteins and nucleic acids. The reason for this distinction
may lie in the levels of architectural control to be found in each
class of polymers; proteins and nucleic acids are characterized by
defined lengths, sequences, and stereochemistries, while synthetic
polymers are highly heterogeneous molecular mixtures. This raises
interesting questions regarding the kinds of materials science that
could be done if new macromolecular architectures could be created
with precise control of the most important structural variables.
Microbial expressions of artificial genes provides a means of doing
just that. The process begins with molecular design--the specification
of a chain structure that the investigator believes will exhibit interesting
(and perhaps useful) behavior. Th target structure is then encoded
into an artificial gene, and the gene is expressed in an appropriate
microbial host. Current targets include novel liquid crystal phases,
macromolecular surface arrays, reversible hydrogels, and artificial
extracellular matrices for use in tissue regeneration and repair.
An important theme of all of these projects is the development of
methods for efficient incorporation of new monomers (beyond the twenty
"normal" amino acids) into artificial proteins in vivo.
The second program under development in the Tirrell group is directed
toward fabrication of nanometer-scale wires, networks, and tubes.
The approach involves patterning of fluid lipid bilayer membranes
via micromanipulation, followed by photopolymerization and crosslinking
of macromonomers confined by the membrane template. The method offers
substantial advantages in comparison with other patterning techniques,
in that it yields flexible structures that can be manipulated readily
in three dimensions. Current efforts are directed toward development
of new patterning chemistries and toward new methods for introduction
of controlled electronic, mechanical, and transport properties.