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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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Detalles Bibliográficos
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
Descripción
Sumario: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.