Search for: All records

Abstract This work investigates the influence of dielectrophoretic forces on the structural features and the resulting aggregates of a chromogenic model system, peptide‐diacetylene (D₃GV‐DA) amphiphiles. Here, we systematically investigate how non‐uniform electric fields impact the (i) peptide‐directed supramolecular assembly stage and (ii) topochemical photopolymerization stage of polydiacetylenes (PDAs) in a quadrupole‐based dielectrophoresis (DEP) device, as well as the (iii) manipulation of D₃GV‐DA aggregates in a light‐induced DEP (LiDEP) platform. The conformation‐dependent chromatic phases of peptide‐PDAs are utilized to probe the chain‐level effect of DEP exposure after the supramolecular assembly or after the topochemical photopolymerization stage. Steady‐state spectroscopic and microscopy analyses show that structural features such as the chirality and morphologies of peptidic 1‐D nanostructures are mostly conserved upon DEP exposure, but applying mild, non‐uniform fields at the self‐assembly stage is sufficient for fine‐tuning the chromatic phase ratio in peptide‐PDAs and manipulating their aggregates via LiDEP. Overall, this work provides insights into how non‐uniform electric fields offer a controllable approach to fine‐tune or preserve the molecularly preset assembly order of DEP‐responsive supramolecular or biopolymeric assemblies, as well as manipulate their aggregates using light projections, which have future implications for the precision fabrication of macromolecular systems with hierarchical structure‐dependent function. 

Abstract Multi‐scale organization of molecular and living components is one of the most critical parameters that regulate charge transport in electroactive systems—whether abiotic, biotic, or hybrid interfaces. In this article, an overview of the current state‐of‐the‐art for controlling molecular order, nanoscale assembly, microstructure domains, and macroscale architectures of electroactive organic interfaces used for biomedical applications is provided. Discussed herein are the leading strategies and challenges to date for engineering the multi‐scale organization of electroactive organic materials, including biomolecule‐based materials, synthetic conjugated molecules, polymers, and their biohybrid analogs. Importantly, this review provides a unique discussion on how the dependence of conduction phenomena on structural organization is observed for electroactive organic materials, as well as for their living counterparts in electrogenic tissues and biotic‐abiotic interfaces. Expansion of fabrication capabilities that enable higher resolution and throughput for the engineering of ordered, patterned, and architecture electroactive systems will significantly impact the future of bioelectronic technologies for medical devices, bioinspired harvesting platforms, and in vitro models of electroactive tissues. In summary, this article presents how ordering at multiple scales is important for modulating transport in both the electroactive organic, abiotic, and living components of bioelectronic systems. 

Abstract Peptides naturally have stimuli‐adaptive structural conformations that are advantageous for endowing synthetic materials with dynamic functionalities. Here, we report a carbodiimide‐based approach, combined with electrostatic modulation, to instruct π‐conjugated peptides to self‐assemble and be responsive to thermal disassembly cues upon consumption of the assembly trigger. Quaterthiophene‐functionalized peptides are utilized as a model system herein to study the formation of nanostructures at non‐equilibrium states. Peptides were designed to have aspartic acid at the termini to allow intramolecular anhydride formation upon adding carbodiimide, which consequentially reduces the electrostatic repulsion and facilitates assembly. We show that the carbodiimide‐fueled assembly and subsequent thermally assisted disassembly can be modulated by the net charge of the peptidic monomers, suggesting an assembly mechanism that can be encoded by sequence design. This carbodiimide‐based approach for the assembly of designer π‐conjugated systems offers a unique opportunity to develop bioelectronic supramolecular materials with controllable formation of dynamic and stimuli‐responsive structures.