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Diffracted X-ray Blinking Tracks Single Protein Motions

Single molecule dynamics studies have begun to use quantum probes. Single particle analysis using cryo-transmission electron microscopy has dramatically improved the resolution when studying protein structures and is shifting towards molecular motion observations. X-ray free-electron lasers are also...

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Autores principales: Sekiguchi, Hiroshi, Kuramochi, Masahiro, Ikezaki, Keigo, Okamura, Yu, Yoshimura, Kazuki, Matsubara, Ken, Chang, Jae-Won, Ohta, Noboru, Kubo, Tai, Mio, Kazuhiro, Suzuki, Yoshio, Chavas, Leonard M. G., Sasaki, Yuji C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269541/
https://www.ncbi.nlm.nih.gov/pubmed/30504916
http://dx.doi.org/10.1038/s41598-018-35468-3
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author Sekiguchi, Hiroshi
Kuramochi, Masahiro
Ikezaki, Keigo
Okamura, Yu
Yoshimura, Kazuki
Matsubara, Ken
Chang, Jae-Won
Ohta, Noboru
Kubo, Tai
Mio, Kazuhiro
Suzuki, Yoshio
Chavas, Leonard M. G.
Sasaki, Yuji C.
author_facet Sekiguchi, Hiroshi
Kuramochi, Masahiro
Ikezaki, Keigo
Okamura, Yu
Yoshimura, Kazuki
Matsubara, Ken
Chang, Jae-Won
Ohta, Noboru
Kubo, Tai
Mio, Kazuhiro
Suzuki, Yoshio
Chavas, Leonard M. G.
Sasaki, Yuji C.
author_sort Sekiguchi, Hiroshi
collection PubMed
description Single molecule dynamics studies have begun to use quantum probes. Single particle analysis using cryo-transmission electron microscopy has dramatically improved the resolution when studying protein structures and is shifting towards molecular motion observations. X-ray free-electron lasers are also being explored as routes for determining single molecule structures of biological entities. Here, we propose a new X-ray single molecule technology that allows observation of molecular internal motion over long time scales, ranging from milliseconds up to 10(3) seconds. Our method uses both low-dose monochromatic X-rays and nanocrystal labelling technology. During monochromatic X-ray diffraction experiments, the intensity of X-ray diffraction from moving single nanocrystals appears to blink because of Brownian motion in aqueous solutions. X-ray diffraction spots from moving nanocrystals were observed to cycle in and out of the Bragg condition. Consequently, the internal motions of a protein molecule labelled with nanocrystals could be extracted from the time trajectory using this diffracted X-ray blinking (DXB) approach. Finally, we succeeded in distinguishing the degree of fluctuation motions of an individual acetylcholine-binding protein (AChBP) interacting with acetylcholine (ACh) using a laboratory X-ray source.
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spelling pubmed-62695412018-12-04 Diffracted X-ray Blinking Tracks Single Protein Motions Sekiguchi, Hiroshi Kuramochi, Masahiro Ikezaki, Keigo Okamura, Yu Yoshimura, Kazuki Matsubara, Ken Chang, Jae-Won Ohta, Noboru Kubo, Tai Mio, Kazuhiro Suzuki, Yoshio Chavas, Leonard M. G. Sasaki, Yuji C. Sci Rep Article Single molecule dynamics studies have begun to use quantum probes. Single particle analysis using cryo-transmission electron microscopy has dramatically improved the resolution when studying protein structures and is shifting towards molecular motion observations. X-ray free-electron lasers are also being explored as routes for determining single molecule structures of biological entities. Here, we propose a new X-ray single molecule technology that allows observation of molecular internal motion over long time scales, ranging from milliseconds up to 10(3) seconds. Our method uses both low-dose monochromatic X-rays and nanocrystal labelling technology. During monochromatic X-ray diffraction experiments, the intensity of X-ray diffraction from moving single nanocrystals appears to blink because of Brownian motion in aqueous solutions. X-ray diffraction spots from moving nanocrystals were observed to cycle in and out of the Bragg condition. Consequently, the internal motions of a protein molecule labelled with nanocrystals could be extracted from the time trajectory using this diffracted X-ray blinking (DXB) approach. Finally, we succeeded in distinguishing the degree of fluctuation motions of an individual acetylcholine-binding protein (AChBP) interacting with acetylcholine (ACh) using a laboratory X-ray source. Nature Publishing Group UK 2018-11-30 /pmc/articles/PMC6269541/ /pubmed/30504916 http://dx.doi.org/10.1038/s41598-018-35468-3 Text en © The Author(s) 2018 Open Access 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. The 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/.
spellingShingle Article
Sekiguchi, Hiroshi
Kuramochi, Masahiro
Ikezaki, Keigo
Okamura, Yu
Yoshimura, Kazuki
Matsubara, Ken
Chang, Jae-Won
Ohta, Noboru
Kubo, Tai
Mio, Kazuhiro
Suzuki, Yoshio
Chavas, Leonard M. G.
Sasaki, Yuji C.
Diffracted X-ray Blinking Tracks Single Protein Motions
title Diffracted X-ray Blinking Tracks Single Protein Motions
title_full Diffracted X-ray Blinking Tracks Single Protein Motions
title_fullStr Diffracted X-ray Blinking Tracks Single Protein Motions
title_full_unstemmed Diffracted X-ray Blinking Tracks Single Protein Motions
title_short Diffracted X-ray Blinking Tracks Single Protein Motions
title_sort diffracted x-ray blinking tracks single protein motions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269541/
https://www.ncbi.nlm.nih.gov/pubmed/30504916
http://dx.doi.org/10.1038/s41598-018-35468-3
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