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Inducing order using nanolaminate templates

Published online by Cambridge University Press:  17 January 2011

Christine A. Orme*
Affiliation:
Lawrence Livermore National Laboratory, Livermore, CA 94550
Babak Sadigh
Affiliation:
Lawrence Livermore National Laboratory, Livermore, CA 94550
Michael P. Surh
Affiliation:
Lawrence Livermore National Laboratory, Livermore, CA 94550
Jennifer A. Vandersall
Affiliation:
Lawrence Livermore National Laboratory, Livermore, CA 94550
Peter Bedrossian
Affiliation:
Lawrence Livermore National Laboratory, Livermore, CA 94550
William D. Wilson
Affiliation:
Lawrence Livermore National Laboratory, Livermore, CA 94550
Troy W. Barbee Jr.*
Affiliation:
Lawrence Livermore National Laboratory, Livermore, CA 94550
Peter T. Beernink
Affiliation:
Children’s Hospital Oakland Research Institute, Oakland, California 94609
*
a)Address correspondence to these authors. e-mail: orme1@llnl.gov
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Abstract

Technological progress in the synthesis and characterization of nanometer-scale structures has improved understanding of molecular and colloidal aggregation, self-assembly, and crystal growth. While substrates are commonly used to control nucleation and growth in metal and semiconductor crystals, their use in protein epitaxy has been limited by the lack of substrate structures commensurate with protein sizes. In this paper we describe the use of polished cross sections of amorphous alumina–silica nanolaminates whose periods varied from 8 to 200 nm in the formation of self-assembled monolayers of the protein macromolecule aspartate transcarbamoylase (ATCase). Scanning force microscopy images of rapidly deposited ATCase demonstrates one-dimensional protein ordering along 13.5 nm wide silica nanolaminate. Numerical studies of irreversible adhesion indicate that patterning can induce a higher degree of ordering by varying the substrate periodicity. We expect this to have implications for nucleation and growth of both two-dimensional crystalline layers and bulk protein crystals.

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Reviews
Copyright
Copyright © Materials Research Society 2011

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References

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