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dc.contributor.author | Frank, Viktoria | en |
dc.contributor.author | Chushkin, Yuriy | en |
dc.contributor.author | Fröhlich, Benjamin | en |
dc.contributor.author | Abuillan, Wasim | en |
dc.contributor.author | Rieger, Harden | en |
dc.contributor.author | Becker, Alexandra S. | en |
dc.contributor.author | Yamamoto, Akihisa | en |
dc.contributor.author | Rossetti, Fernanda F. | en |
dc.contributor.author | Kaufmann, Stefan | en |
dc.contributor.author | Lanzer, Michael | en |
dc.contributor.author | Zontone, Federico | en |
dc.contributor.author | Tanaka, Motomu | en |
dc.contributor.alternative | 山本, 暁久 | ja |
dc.contributor.alternative | 田中, 求 | ja |
dc.date.accessioned | 2018-11-26T01:34:55Z | - |
dc.date.available | 2018-11-26T01:34:55Z | - |
dc.date.issued | 2017-10-26 | - |
dc.identifier.issn | 2045-2322 | - |
dc.identifier.uri | http://hdl.handle.net/2433/235330 | - |
dc.description.abstract | Lensless, coherent X-ray diffraction microscopy has been drawing considerable attentions for tomographic imaging of whole human cells. In this study, we performed cryogenic coherent X-ray diffraction imaging of human erythrocytes with and without malaria infection. To shed light on structural features near the surface, “ghost cells” were prepared by the removal of cytoplasm. From two-dimensional images, we found that the surface of erythrocytes after 32 h of infection became much rougher compared to that of healthy, uninfected erythrocytes. The Gaussian roughness of an infected erythrocyte surface (69 nm) is about two times larger than that of an uninfected one (31 nm), reflecting the formation of protein knobs on infected erythrocyte surfaces. Three-dimensional tomography further enables to obtain images of the whole cells with no remarkable radiation damage, whose accuracy was estimated using phase retrieval transfer functions to be as good as 64 nm for uninfected and 80 nm for infected erythrocytes, respectively. Future improvements in phase retrieval algorithm, increase in degree of coherence, and higher flux in combination with complementary X-ray fluorescence are necessary to gain both structural and chemical details of mesoscopic architectures, such as cytoskeletons, membraneous structures, and protein complexes, in frozen hydrated human cells, especially under diseased states. | en |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | - |
dc.publisher | Springer Nature | en |
dc.rights | © The Author(s) 2017. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. Te images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. | en |
dc.title | Lensless Tomographic Imaging of Near Surface Structures of Frozen Hydrated Malaria-Infected Human Erythrocytes by Coherent X-Ray Diffraction Microscopy | en |
dc.type | journal article | - |
dc.type.niitype | Journal Article | - |
dc.identifier.jtitle | Scientific Reports | en |
dc.identifier.volume | 7 | - |
dc.relation.doi | 10.1038/s41598-017-14586-4 | - |
dc.textversion | publisher | - |
dc.identifier.artnum | 14081 | - |
dc.address | Physical Chemistry of Biosystems, Institute of Physical Chemistry, University of Heidelberg | en |
dc.address | European Synchrotron Radiation Facility (ESRF) | en |
dc.address | Physical Chemistry of Biosystems, Institute of Physical Chemistry, University of Heidelberg | en |
dc.address | Physical Chemistry of Biosystems, Institute of Physical Chemistry, University of Heidelberg | en |
dc.address | Physical Chemistry of Biosystems, Institute of Physical Chemistry, University of Heidelberg・Department of Infectious Diseases, Parasitology, University of Heidelberg, 69120, Heidelberg | en |
dc.address | Physical Chemistry of Biosystems, Institute of Physical Chemistry, University of Heidelberg | en |
dc.address | Physical Chemistry of Biosystems, Institute of Physical Chemistry, University of Heidelberg・Institute for Integrated Cell-Material Sciences (WPI iCeMS), Kyoto University | en |
dc.address | Physical Chemistry of Biosystems, Institute of Physical Chemistry, University of Heidelberg・Institute for Integrated Cell-Material Sciences (WPI iCeMS), Kyoto University | en |
dc.address | Physical Chemistry of Biosystems, Institute of Physical Chemistry, University of Heidelberg | en |
dc.address | Department of Infectious Diseases, Parasitology, University of Heidelberg, 69120, Heidelberg | en |
dc.address | European Synchrotron Radiation Facility (ESRF) | en |
dc.address | Physical Chemistry of Biosystems, Institute of Physical Chemistry, University of Heidelberg・Institute for Integrated Cell-Material Sciences (WPI iCeMS), Kyoto University | en |
dc.identifier.pmid | 29074975 | - |
dcterms.accessRights | open access | - |
datacite.awardNumber | 17H00855 | - |
datacite.awardNumber | 26800223 | - |
datacite.awardNumber | 16K05515 | - |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName | 日本学術振興会 | ja |
jpcoar.funderName.alternative | Japan Society for the Promotion of Science (JSPS) | en |
jpcoar.funderName.alternative | Japan Society for the Promotion of Science (JSPS) | en |
jpcoar.funderName.alternative | Japan Society for the Promotion of Science (JSPS) | en |
出現コレクション: | 学術雑誌掲載論文等 |
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