Volume 50, Issue 5 pp. 1533-1540
research papers
Open Access

Nanocrystallography measurements of early stage synthetic malaria pigment

Ruben A. Dilanian

Ruben A. Dilanian

ARC Centre of Excellence in Advanced Molecular Imaging, School of Physics, The University of Melbourne, Melbourne, Victoria3010, Australia

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Victor Streltsov

Victor Streltsov

CSIRO, Parkville, Victoria3052, Australia

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Hannah D. Coughlan

Hannah D. Coughlan

ARC Centre of Excellence in Advanced Molecular Imaging, Department of Chemistry and Physics, La Trobe Institute for Molecular Science, La Trobe University, Melbourne, Victoria3086, Australia

The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria 3052, Australia

CSIRO Manufacturing Flagship, Parkville, Victoria, Australia

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Harry M. Quiney

Harry M. Quiney

ARC Centre of Excellence in Advanced Molecular Imaging, School of Physics, The University of Melbourne, Melbourne, Victoria3010, Australia

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Andrew V. Martin

Andrew V. Martin

ARC Centre of Excellence in Advanced Molecular Imaging, School of Physics, The University of Melbourne, Melbourne, Victoria3010, Australia

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Nectarios Klonis

Nectarios Klonis

Department of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, Victoria3010, Australia

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Con Dogovski

Con Dogovski

Department of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, Victoria3010, Australia

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Sébastien Boutet

Sébastien Boutet

LiNAC Coherent Light Source, SLAC National Accelerator Laboratory, Menlo Park, CA 94025, USA

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Marc Messerschmidt

Marc Messerschmidt

BioXFEL STC, 700 Ellicott Street, Buffalo, NY 1420, USA

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Garth J. Williams

Garth J. Williams

Brookhaven National Laboratory, PO Box 5000, Upton, NY 11973-5000, USA

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Sophie Williams

Sophie Williams

ARC Centre of Excellence in Advanced Molecular Imaging, School of Physics, The University of Melbourne, Melbourne, Victoria3010, Australia

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Nicholas W. Phillips

Nicholas W. Phillips

CSIRO, Parkville, Victoria3052, Australia

ARC Centre of Excellence in Advanced Molecular Imaging, Department of Chemistry and Physics, La Trobe Institute for Molecular Science, La Trobe University, Melbourne, Victoria3086, Australia

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Keith A. Nugent

Keith A. Nugent

ARC Centre of Excellence in Advanced Molecular Imaging, Department of Chemistry and Physics, La Trobe Institute for Molecular Science, La Trobe University, Melbourne, Victoria3086, Australia

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Leann Tilley

Corresponding Author

Leann Tilley

Department of Biochemistry and Molecular Biology, Bio21 Molecular Science and Biotechnology Institute, The University of Melbourne, Melbourne, Victoria3010, Australia

Leann Tilley, e-mail: [email protected]; Brian Abbey, e-mail: [email protected]Search for more papers by this author
Brian Abbey

Corresponding Author

Brian Abbey

ARC Centre of Excellence in Advanced Molecular Imaging, Department of Chemistry and Physics, La Trobe Institute for Molecular Science, La Trobe University, Melbourne, Victoria3086, Australia

Leann Tilley, e-mail: [email protected]; Brian Abbey, e-mail: [email protected]Search for more papers by this author
First published: 29 September 2017
Citations: 2

Abstract

The recent availability of extremely intense, femtosecond X-ray free-electron laser (XFEL) sources has spurred the development of serial femtosecond nanocrystallography (SFX). Here, SFX is used to analyze nanoscale crystals of β-hematin, the synthetic form of hemozoin which is a waste by-product of the malaria parasite. This analysis reveals significant differences in β-hematin data collected during SFX and synchrotron crystallography experiments. To interpret these differences two possibilities are considered: structural differences between the nanocrystal and larger crystalline forms of β-hematin, and radiation damage. Simulation studies show that structural inhomogeneity appears at present to provide a better fit to the experimental data. If confirmed, these observations will have implications for designing compounds that inhibit hemozoin formation and suggest that, for some systems at least, additional information may be gained by comparing structures obtained from nanocrystals and macroscopic crystals of the same molecule.

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