Spontaneous and X-ray–Triggered Crystallization at Long Range in Self-Assembling Filament Networks

Author:

Cui Honggang1,Pashuck E. Thomas1,Velichko Yuri S.1,Weigand Steven J.2,Cheetham Andrew G.3,Newcomb Christina J.1,Stupp Samuel I.1345

Affiliation:

1. Department of Materials Science and Engineering, Northwestern University, 2220 Campus Drive, Evanston, IL 60208, USA.

2. DuPont-Northwestern-Dow Collaborative Access Team (DND-CAT) Synchrotron Research Center, Northwestern University, Advanced Photon Source (APS)/Argonne National Laboratory 432-A004, 9700 South Cass Avenue, Argonne, IL 60439, USA.

3. Institute for BioNanotechnology in Medicine, Northwestern University, Chicago, IL 60611, USA.

4. Department of Chemistry, Northwestern University, 2220 Campus Drive, Evanston, IL 60208, USA.

5. Department of Medicine, Northwestern University, 2220 Campus Drive, Evanston, IL 60208, USA.

Abstract

X-rays to Order Self-assembly of molecules is often irreversible. Cui et al. (p. 555 , published online 17 December; see the Perspective by Safinya and Li ) examined the ordering of a short peptide sequence (Ala 6 Glu 3 ) terminated with an alkyl chain. Aqueous solutions of this molecule could form hexagonally ordered filaments, but more dilute solutions were disordered. However, prolonged x-ray exposure caused these arrays to become ordered. These arrays were stable for several hours but eventually returned to a disordered state; the addition of salts slowed the ordering processes. It is possible that during the ordering process, X-ray–induced charging affected the repulsive forces that balance tension within the filament.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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