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Development of the field of structural physiology

Electron crystallography is especially useful for studying the structure and function of membrane proteins — key molecules with important functions in neural and other cells. Electron crystallography is now an established technique for analyzing the structures of membrane proteins in lipid bilayers...

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Autor principal: FUJIYOSHI, Yoshinori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Japan Academy 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754503/
https://www.ncbi.nlm.nih.gov/pubmed/26560835
http://dx.doi.org/10.2183/pjab.91.447
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author FUJIYOSHI, Yoshinori
author_facet FUJIYOSHI, Yoshinori
author_sort FUJIYOSHI, Yoshinori
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description Electron crystallography is especially useful for studying the structure and function of membrane proteins — key molecules with important functions in neural and other cells. Electron crystallography is now an established technique for analyzing the structures of membrane proteins in lipid bilayers that closely simulate their natural biological environment. Utilizing cryo-electron microscopes with helium-cooled specimen stages that were developed through a personal motivation to understand the functions of neural systems from a structural point of view, the structures of membrane proteins can be analyzed at a higher than 3 Å resolution. This review covers four objectives. First, I introduce the new research field of structural physiology. Second, I recount some of the struggles involved in developing cryo-electron microscopes. Third, I review the structural and functional analyses of membrane proteins mainly by electron crystallography using cryo-electron microscopes. Finally, I discuss multifunctional channels named “adhennels” based on structures analyzed using electron and X-ray crystallography.
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spelling pubmed-47545032016-02-26 Development of the field of structural physiology FUJIYOSHI, Yoshinori Proc Jpn Acad Ser B Phys Biol Sci Review Electron crystallography is especially useful for studying the structure and function of membrane proteins — key molecules with important functions in neural and other cells. Electron crystallography is now an established technique for analyzing the structures of membrane proteins in lipid bilayers that closely simulate their natural biological environment. Utilizing cryo-electron microscopes with helium-cooled specimen stages that were developed through a personal motivation to understand the functions of neural systems from a structural point of view, the structures of membrane proteins can be analyzed at a higher than 3 Å resolution. This review covers four objectives. First, I introduce the new research field of structural physiology. Second, I recount some of the struggles involved in developing cryo-electron microscopes. Third, I review the structural and functional analyses of membrane proteins mainly by electron crystallography using cryo-electron microscopes. Finally, I discuss multifunctional channels named “adhennels” based on structures analyzed using electron and X-ray crystallography. The Japan Academy 2015-11-11 /pmc/articles/PMC4754503/ /pubmed/26560835 http://dx.doi.org/10.2183/pjab.91.447 Text en © 2015 The Japan Academy This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
FUJIYOSHI, Yoshinori
Development of the field of structural physiology
title Development of the field of structural physiology
title_full Development of the field of structural physiology
title_fullStr Development of the field of structural physiology
title_full_unstemmed Development of the field of structural physiology
title_short Development of the field of structural physiology
title_sort development of the field of structural physiology
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754503/
https://www.ncbi.nlm.nih.gov/pubmed/26560835
http://dx.doi.org/10.2183/pjab.91.447
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