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Proceedings Paper

Sub-100-nm 3D-elemental mapping of frozen-hydrated cells using the bionanoprobe
Author(s): Si Chen; Ye Yuan; Junjing Deng; Rachel Mak; Qiaoling Jin; Tatjana Paunesku; Sophie C. Gleber; David Vine; Claus Flachenecker; Benjamin Hornberger; Deming Shu; Barry Lai; Jörg Maser; Lydia Finney; Christian Roehrig; Jay VonOsinski; Michael Bolbat; Keith Brister; Chris Jacobsen; Gayle Woloschak; Stefan Vogt
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Paper Abstract

Hard X-ray fluorescence microscopy is one of the most sensitive techniques to perform trace elemental analysis of unsectioned biological samples, such as cells and tissues. As the spatial resolution increases beyond sub-micron scale, conventional sample preparation method, which involves dehydration, may not be sufficient for preserving subcellular structures in the context of radiation-induced artifacts. Imaging of frozen-hydrated samples under cryogenic conditions is the only reliable way to fully preserve the three dimensional structures of the samples while minimizing the loss of diffusible ions. To allow imaging under this hydrated “natural-state” condition, we have developed the Bionanoprobe (BNP), a hard X-ray fluorescence nanoprobe with cryogenic capabilities, dedicated to studying trace elements in frozen-hydrated biological systems. The BNP is installed at an undulator beamline at Life Sciences Collaboration Access Team at the Advanced Photon Source. It provides a spatial resolution of 30 nm for fluorescence imaging by using Fresnel zone plates as nanofocusing optics. Differential phase contrast imaging is carried out in parallel to fluorescence imaging by using a quadrant photodiode mounted downstream of the sample. By employing a liquid-nitrogen-cooled sample stage and cryo specimen transfer mechanism, the samples are well maintained below 110 K during both transfer and X-ray imaging. The BNP is capable for automated tomographic dataset collection, which enables visualization of internal structures and composition of samples in a nondestructive manner. In this presentation, we will describe the instrument design principles, quantify instrument performance, and report the early results that were obtained from frozen-hydrated whole cells.

Paper Details

Date Published: 26 September 2013
PDF: 7 pages
Proc. SPIE 8851, X-Ray Nanoimaging: Instruments and Methods, 885102 (26 September 2013); doi: 10.1117/12.2025169
Show Author Affiliations
Si Chen, Argonne National Lab. (United States)
Ye Yuan, Northwestern Univ. (United States)
Junjing Deng, Northwestern Univ. (United States)
Rachel Mak, Northwestern Univ. (United States)
Qiaoling Jin, Northwestern Univ. (United States)
Tatjana Paunesku, Northwestern Univ. (United States)
Sophie C. Gleber, Argonne National Lab. (United States)
David Vine, Argonne National Lab. (United States)
Claus Flachenecker, Carl Zeiss X-ray Microscopy, Inc. (United States)
Benjamin Hornberger, Carl Zeiss X-ray Microscopy, Inc. (United States)
Deming Shu, Argonne National Lab. (United States)
Barry Lai, Argonne National Lab. (United States)
Jörg Maser, Argonne National Lab. (United States)
Lydia Finney, Argonne National Lab. (United States)
Christian Roehrig, Argonne National Lab. (United States)
Jay VonOsinski, Northwestern Synchrotron Research Ctr. (United States)
Michael Bolbat, Northwestern Synchrotron Research Ctr. (United States)
Keith Brister, Northwestern Synchrotron Research Ctr. (United States)
Chris Jacobsen, Argonne National Lab. (United States)
Gayle Woloschak, Northwestern Univ. (United States)
Stefan Vogt, Argonne National Lab. (United States)

Published in SPIE Proceedings Vol. 8851:
X-Ray Nanoimaging: Instruments and Methods
Barry Lai, Editor(s)

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