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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Veröffentlicht in:Scientific reports 2018-11, Vol.8 (1), p.17090-8, Article 17090
Hauptverfasser: 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.
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Sprache:eng
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Zusammenfassung: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.
ISSN:2045-2322
2045-2322
DOI:10.1038/s41598-018-35468-3