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- W2037102023 abstract "Molecular self-assembly at equilibrium is fundamental to the fields of biological self-organization, the development of novel environmentally responsive polymeric materials, and nanofabrication. Our approach to understanding the principles governing this process is inspired by existing models and measurements for the self-assembly of actin, tubulin, and the ubiquitous icosahedral shell structures of viral capsids. We introduce a family of simple potentials that give rise to the self-assembly of linear polymeric, random surface (``membrane''), tubular (``nanotube''), and hollow icosahedral structures that are similar in many respects to their biological counterparts. The potentials involve and an interplay between directional (dipolar, multipolar) and short-range (van der Waals) interactions. Specifically, we find that the dipolar potential, having a continuous rotational symmetry about the dipolar axis, gives rise to chain formation, while particles with multipolar potentials, having discrete rotational symmetries (square quadrupole or triangular ring of dipoles or ``hexapole''), lead to the self-assembly of open sheet, nanotube, and hollow icosahedral geometries. These changes in the geometry of self-assembly are accompanied by significant changes in the kinetics of the organization." @default.
- W2037102023 created "2016-06-24" @default.
- W2037102023 creator A5023304618 @default.
- W2037102023 creator A5044313983 @default.
- W2037102023 date "2006-03-07" @default.
- W2037102023 modified "2023-09-29" @default.
- W2037102023 title "Symmetry, equivalence, and molecular self-assembly" @default.
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