2007 APS March Meeting
Volume 52, Number 1
Monday–Friday, March 5–9, 2007;
Denver, Colorado
Session L24: John H. Dillon Award Symposium
2:30 PM–5:30 PM,
Tuesday, March 6, 2007
Colorado Convention Center
Room: 201
Sponsoring
Unit:
DPOLY
Chair: Tim Bunning, Wright Patterson Air Force Base
Abstract ID: BAPS.2007.MAR.L24.1
Abstract: L24.00001 : Swell Gels to Dumbbell Micelles: Construction of Materials and Nanostructure with Self-assembly
2:30 PM–3:06 PM
Preview Abstract
Abstract
Author:
Darrin Pochan
(University of Delaware)
Bionanotechnology, the emerging field of using biomolecular and biotechnological
tools for nanostructure or nanotecnology development, provides exceptional
opportunity in the design of new materials. Self-assembly of molecules is an
attractive materials construction strategy due to its simplicity in application. By
considering peptidic or charged synthetic polymer molecules in the bottom-up
materials self-assembly design process, one can take advantage of inherently
biomolecular attributes; intramolecular folding events, secondary structure, and
electrostatic interactions; in addition to more traditional self-assembling molecular
attributes such as amphiphilicty, to define hierarchical material structure and
consequent properties. Several molecular systems will be discussed. Synthetic
block copolymers with charged corona blocks can be assembled in dilute solution
containing multivalent organic counterions to produce micelle structures such as
toroids. These ring-like micelles are similar to the toroidal bundling of charged
semiflexible biopolymers like DNA in the presence of multivalent counterions.
Micelle structure can be tuned between toroids, cylinders, and disks simply by using
different concentrations or molecular volumes of organic counterion. In addition,
these charged blocks can consist of amino acids as monomers producing block
copolypeptides. In addition to the above attributes, block copolypeptides provide
the control of block secondary structure to further control self-assembly. Design
strategies based on small (less than 24 amino acids) beta-hairpin peptides will be
discussed. Self-assembly of the peptides is predicated on an intramolecular folding
event caused by desired solution properties. Importantly, the intramolecular folding
event impart a molecular-level mechanism for environmental responsiveness at the
material level (e.g. infinite change in viscosity of a solution to a gel with changes in
pH, ionic strength, temperature).
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2007.MAR.L24.1