APS March Meeting 2017
Volume 62, Number 4
Monday–Friday, March 13–17, 2017;
New Orleans, Louisiana
Session B21: Biopolymer Physics
11:15 AM–2:15 PM,
Monday, March 13, 2017
Room: 281-282
Sponsoring
Units:
DPOLY DBIO
Chair: Brad Olsen, MIT
Abstract ID: BAPS.2017.MAR.B21.3
Abstract: B21.00003 : 2-d and 1-d Nanomaterials Construction through Peptide Computational Design and Solution Assembly*
12:27 PM–1:03 PM
Preview Abstract
Abstract
Author:
Darrin Pochan
(University of Delaware)
Self-assembly of molecules is an attractive materials construction strategy
due to its simplicity in application. By considering peptidic 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/H-bonding/hydrophobic interactions to
define hierarchical material structure and consequent properties.
Importantly, while biomimicry has been a successful strategy for the design
of new peptide molecules for intermolecular assembly, computational tools
have been developed to de novo design peptide molecules required for
construction of pre-determined, desired nanostructures and materials. A new
system comprised of coiled coil bundle motifs theoretically designed to
assemble into designed, one and two-dimensional nanostructures will be
introduced. The strategy provides the opportunity for arbitrary
nanostructure formation, i.e. structures not observed in nature, with
peptide molecules. Importantly, the desired nanostructure was chosen first
while the peptides needed for coiled coil formation and subsequent
nanomaterial formation were determined computationally. Different
interbundle, two-dimensional nanostructures are stabilized by differences in
amino acid composition exposed on the exterior of the coiled coil bundles.
Computation was able to determine molecules required for different
interbundle symmetries within two-dimensional sheets stabilized by subtle
differences in amino acid composition of the inherent peptides. Finally,
polymers were also created through covalent interactions between bundles
that allowed formation of architectures spanning flexible network forming
chains to ultra-stiff polymers, all with the same building block peptides.
The success of the computational design strategy is manifested in the
nanomaterial results as characterized by electron microscopy, scattering
methods, and biophysical techniques.
*Support from NSF DMREF program under awards DMR-1234161 and DMR-1235084
To cite this abstract, use the following reference: http://meetings.aps.org/link/BAPS.2017.MAR.B21.3