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Materials Science and Engineering Colloquium

Event Type
Materials Science and Engineering
100 Materials Science and Engineering Building
Nov 13, 2017   4:00 pm  
Darrin Pochan, Materials Science and Engineering, University of Delaware
Originating Calendar
MatSE Seminars

 "Biomolecules for non-biological things: Materials construction through peptide design and solution assembly"


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 interactions; in addition to more traditional self-assembling molecular attributes such as amphiphilicty, to define hierarchical material structure and consequent properties. Furthermore, different self-assembly pathways can be utilized to reproducibly form different nanostructures with the same molecule design. Two classes of materials will be discussed. First, the local nano- and overall network structure, and resultant viscoelastic and cell-level biological properties, of hydrogels that are formed via beta-hairpin self-assembly will be presented. Importantly, the hydrogels do not form until individual peptide molecules intramolecularly fold into a beta-hairpin conformation. Subsequently, specific, intermolecular assembly occurs into a branched nanofibrillar network. These peptide hydrogels are potentially excellent scaffolds for tissue repair and regeneration due to inherent cytocompatibility, porous morphology, and shear-thinning but instant recovery viscoelastic properties. During assembly and gelation, desired components can be encapsulated within the hydrogel network such as drug compounds and/or living cells. The system can shear thin but immediately reheal to preshear stiffness on the cessation of the shear stress. Second, a new solution assembled system comprised of coiled coil motifs designed theoretically to assemble into two-dimensional nanostructures not observed in nature will be introduced. The molecules and nanostructures are not natural sequences and provide opportunity for arbitrary nanostructure creation with peptides. New results revealing the versatility of computational design of peptide building blocks for physical and covalent interaction to build new forms of one-dimensional chains and two-dimensional network materials will be discussed.


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