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Updated: Jan 8, 2026

Formation of Ordered Biomolecular Structures by the Self-assembly of Short Peptides
Published on: November 21, 2013
Electrostatic Coassembly of Coiled-Coil Peptide Bundlemers with Complementary Charges into Porous 2D Lattices
Weiran Xie1, Tianren Zhang1,2, Rui Guo2
1Department of Materials Science and Engineering, University of Delaware, Newark, Delaware 19716, United States.
Abstract:
A series of highly charged coiled-coil peptide particles, or "bundlemers," with only a single charge type in a bundlemer particle (i.e., either all positive charges or all negative charges) were computationally designed with varied charge spatial display and amino acid types. Electrostatic complexation of oppositely charged single-charge-type peptide bundlemers resulted in the formation of well-defined porous lattices. Structural characterization using electron microscopy and small-angle X-ray scattering revealed that the lattice morphology is modulated by the charged side-chain spatial arrangement on the coiled-coil particle surfaces and the relative stoichiometry of surface charges in mixtures of oppositely charged bundlemer particles. Furthermore, alterations in the side-chain length and type of charged side chains on the coiled-coil particle surfaces enabled further control of lattice formation. Lattice assembly through single-charge bundlemer complexation is in stark contrast to the amorphous structures formed using bundlemer coiled-coil particles with mixed-charge character (i.e., containing both negatively and positively charged amino acids in the same particle). These results provide a robust framework for supramolecular nanostructure formation through rational surface charge manipulation of bundlemer building blocks.
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