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Second harmonic generation polarization microscopy as a tool for protein structure analysis

Cryo-electron microscopy and X-ray crystallography have been the major tools of protein structure analysis for decades and will certainly continue to be essential in the future. Moreover, nuclear magnetic resonance or Förster resonance energy transfer can measure structural dynamics. Here, we propos...

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Autores principales: Kaneshiro, Junichi, Okada, Yasushi, Shima, Tomohiro, Tsujii, Mika, Imada, Katsumi, Ichimura, Taro, Watanabe, Tomonobu M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Biophysical Society of Japan (BSJ) 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812877/
https://www.ncbi.nlm.nih.gov/pubmed/31660282
http://dx.doi.org/10.2142/biophysico.16.0_147
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author Kaneshiro, Junichi
Okada, Yasushi
Shima, Tomohiro
Tsujii, Mika
Imada, Katsumi
Ichimura, Taro
Watanabe, Tomonobu M.
author_facet Kaneshiro, Junichi
Okada, Yasushi
Shima, Tomohiro
Tsujii, Mika
Imada, Katsumi
Ichimura, Taro
Watanabe, Tomonobu M.
author_sort Kaneshiro, Junichi
collection PubMed
description Cryo-electron microscopy and X-ray crystallography have been the major tools of protein structure analysis for decades and will certainly continue to be essential in the future. Moreover, nuclear magnetic resonance or Förster resonance energy transfer can measure structural dynamics. Here, we propose to add optical second-harmonic generation (SHG), which is a nonlinear optical scattering process sensitive to molecular structures in illuminated materials, to the tool-kit of structural analysis methodologies. SHG can be expected to probe the structural changes of proteins in the physiological condition, and thus link protein structure and biological function. We demonstrate that a conformational change as well as its dynamics in protein macromolecular assemblies can be detected by means of SHG polarization measurement. To prove the capability of SHG polarization measurement with regard to protein structure analysis, we developed an SHG polarization microscope to analyze microtubules in solution. The difference in conformation between microtubules with different binding molecules was successfully observed as polarization dependence of SHG intensity. We also succeeded in capturing the temporal variation of structure in a photo-switchable protein crystal in both activation and inactivation processes. These results illustrate the potential of this method for protein structure analysis in physiological solutions at room temperature without any labeling.
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spelling pubmed-68128772019-10-28 Second harmonic generation polarization microscopy as a tool for protein structure analysis Kaneshiro, Junichi Okada, Yasushi Shima, Tomohiro Tsujii, Mika Imada, Katsumi Ichimura, Taro Watanabe, Tomonobu M. Biophys Physicobiol Regular Article Cryo-electron microscopy and X-ray crystallography have been the major tools of protein structure analysis for decades and will certainly continue to be essential in the future. Moreover, nuclear magnetic resonance or Förster resonance energy transfer can measure structural dynamics. Here, we propose to add optical second-harmonic generation (SHG), which is a nonlinear optical scattering process sensitive to molecular structures in illuminated materials, to the tool-kit of structural analysis methodologies. SHG can be expected to probe the structural changes of proteins in the physiological condition, and thus link protein structure and biological function. We demonstrate that a conformational change as well as its dynamics in protein macromolecular assemblies can be detected by means of SHG polarization measurement. To prove the capability of SHG polarization measurement with regard to protein structure analysis, we developed an SHG polarization microscope to analyze microtubules in solution. The difference in conformation between microtubules with different binding molecules was successfully observed as polarization dependence of SHG intensity. We also succeeded in capturing the temporal variation of structure in a photo-switchable protein crystal in both activation and inactivation processes. These results illustrate the potential of this method for protein structure analysis in physiological solutions at room temperature without any labeling. The Biophysical Society of Japan (BSJ) 2019-09-20 /pmc/articles/PMC6812877/ /pubmed/31660282 http://dx.doi.org/10.2142/biophysico.16.0_147 Text en 2019 © The Biophysical Society of Japan This article is licensed under the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License. To view a copy of this license, visit https://creativecommons.org/licenses/by-nc-sa/4.0/.
spellingShingle Regular Article
Kaneshiro, Junichi
Okada, Yasushi
Shima, Tomohiro
Tsujii, Mika
Imada, Katsumi
Ichimura, Taro
Watanabe, Tomonobu M.
Second harmonic generation polarization microscopy as a tool for protein structure analysis
title Second harmonic generation polarization microscopy as a tool for protein structure analysis
title_full Second harmonic generation polarization microscopy as a tool for protein structure analysis
title_fullStr Second harmonic generation polarization microscopy as a tool for protein structure analysis
title_full_unstemmed Second harmonic generation polarization microscopy as a tool for protein structure analysis
title_short Second harmonic generation polarization microscopy as a tool for protein structure analysis
title_sort second harmonic generation polarization microscopy as a tool for protein structure analysis
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6812877/
https://www.ncbi.nlm.nih.gov/pubmed/31660282
http://dx.doi.org/10.2142/biophysico.16.0_147
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