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Imaging live cell in micro-liquid enclosure by X-ray laser diffraction
Emerging X-ray free-electron lasers with femtosecond pulse duration enable single-shot snapshot imaging almost free from sample damage by outrunning major radiation damage processes. In bioimaging, it is essential to keep the sample close to its natural state. Conventional high-resolution imaging, h...
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Published in: | Nature communications 2014-01, Vol.5 (1), p.3052-3052, Article 3052 |
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Main Authors: | , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Emerging X-ray free-electron lasers with femtosecond pulse duration enable single-shot snapshot imaging almost free from sample damage by outrunning major radiation damage processes. In bioimaging, it is essential to keep the sample close to its natural state. Conventional high-resolution imaging, however, suffers from severe radiation damage that hinders live cell imaging. Here we present a method for capturing snapshots of live cells kept in a micro-liquid enclosure array by X-ray laser diffraction. We place living
Microbacterium lacticum
cells in an enclosure array and successively expose each enclosure to a single X-ray laser pulse from the SPring-8 Angstrom Compact Free-Electron Laser. The enclosure itself works as a guard slit and allows us to record a coherent diffraction pattern from a weakly-scattering submicrometre-sized cell with a clear fringe extending up to a 28-nm full-period resolution. The reconstructed image reveals living whole-cell structures without any staining, which helps advance understanding of intracellular phenomena.
Live cell imaging at high resolution is very challenging because cells die upon prolonged radiation exposure. Kimura
et al.
overcome this problem by using pulsed coherent X-ray diffraction to image live microbacterium in a nanofabricated liquid enclosure at resolution far exceeding optical methods. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/ncomms4052 |