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Self-replicating colloidal clusters

Zorana Zeravcic and Michael P. Brenner
PNAS published ahead of print January 21, 2014 https://doi.org/10.1073/pnas.1313601111
Zorana Zeravcic
aSchool of Engineering and Applied Sciences andbKavli Institute for Bionano Science and Technology, Harvard University, Cambridge, MA 02138
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  • For correspondence: zorana@seas.harvard.edu
Michael P. Brenner
aSchool of Engineering and Applied Sciences andbKavli Institute for Bionano Science and Technology, Harvard University, Cambridge, MA 02138
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  1. Edited by Paul M. Chaikin, New York University, New York, NY, and approved December 23, 2013 (received for review July 18, 2013)

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Significance

One of the hallmarks of living systems is self-replication. Mimicking nature’s ability to self-replicate would not only give more insight into biological mechanisms of self-replication but also could potentially revolutionize material science and nanotechnology. Over the past 60 y, much research, both theoretical and experimental, has been focused on understanding and realizing self-replicating systems. However, artificial systems that efficiently self-replicate remained elusive. In this paper, we construct schemes for self-replication of small clusters of isotropic particles. By manipulating the energy landscape of the process, we show how exponential replication can be achieved. As a proof of principle, we show exponential self-replication of an octahedral cluster using finite-temperature computer simulations.

Abstract

We construct schemes for self-replicating clusters of spherical particles, validated with computer simulations in a finite-temperature heat bath. Each particle has stickers uniformly distributed over its surface, and the rules for self-replication are encoded into the specificity and strength of interactions. Geometrical constraints imply that a compact cluster can copy itself only with help of a catalyst, a smaller cluster that increases the surface area to form a template. Replication efficiency requires optimizing interaction energies to destabilize all kinetic traps along the reaction pathway, as well as initiating a trigger event that specifies when the new cluster disassociates from its parent. Although there is a reasonably wide parameter range for self-replication, there is a subtle balance between the speed of the reaction, and the error rate. As a proof of principle, we construct interactions that self-replicate an octahedron, requiring a two-particle dimer for a catalyst. The resulting self-replication scheme is a hypercycle, and computer simulations confirm the exponential growth of both octahedron and catalyst replicas.

  • self-assembly
  • catalytic cycle

Footnotes

  • ↵1To whom correspondence should be addressed. E-mail: zorana{at}seas.harvard.edu.
  • Author contributions: Z.Z. and M.P.B. designed research, performed research, analyzed data, and wrote the paper.

  • The authors declare no conflict of interest.

  • This article is a PNAS Direct Submission.

  • This article contains supporting information online at www.pnas.org/lookup/suppl/doi:10.1073/pnas.1313601111/-/DCSupplemental.

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Self-replicating colloidal clusters
Zorana Zeravcic, Michael P. Brenner
Proceedings of the National Academy of Sciences Jan 2014, 201313601; DOI: 10.1073/pnas.1313601111

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Self-replicating colloidal clusters
Zorana Zeravcic, Michael P. Brenner
Proceedings of the National Academy of Sciences Jan 2014, 201313601; DOI: 10.1073/pnas.1313601111
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