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Studying membrane proteins with MicroED

The structural investigation of biological macromolecules is indispensable in understanding the molecular mechanisms underlying diseases. Several structural biology techniques have been introduced to unravel the structural facets of biomolecules. Among these, the electron cryomicroscopy (cryo-EM) me...

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Detalles Bibliográficos
Autores principales: Gallenito, Marc J., Gonen, Tamir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9022970/
https://www.ncbi.nlm.nih.gov/pubmed/35191473
http://dx.doi.org/10.1042/BST20210911
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author Gallenito, Marc J.
Gonen, Tamir
author_facet Gallenito, Marc J.
Gonen, Tamir
author_sort Gallenito, Marc J.
collection PubMed
description The structural investigation of biological macromolecules is indispensable in understanding the molecular mechanisms underlying diseases. Several structural biology techniques have been introduced to unravel the structural facets of biomolecules. Among these, the electron cryomicroscopy (cryo-EM) method microcrystal electron diffraction (MicroED) has produced atomic resolution structures of important biological and small molecules. Since its inception in 2013, MicroED established a demonstrated ability for solving structures of difficult samples using vanishingly small crystals. However, membrane proteins remain the next big frontier for MicroED. The intrinsic properties of membrane proteins necessitate improved sample handling and imaging techniques to be developed and optimized for MicroED. Here, we summarize the milestones of electron crystallography of two-dimensional crystals leading to MicroED of three-dimensional crystals. Then, we focus on four different membrane protein families and discuss representatives from each family solved by MicroED.
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spelling pubmed-90229702022-05-03 Studying membrane proteins with MicroED Gallenito, Marc J. Gonen, Tamir Biochem Soc Trans Review Articles The structural investigation of biological macromolecules is indispensable in understanding the molecular mechanisms underlying diseases. Several structural biology techniques have been introduced to unravel the structural facets of biomolecules. Among these, the electron cryomicroscopy (cryo-EM) method microcrystal electron diffraction (MicroED) has produced atomic resolution structures of important biological and small molecules. Since its inception in 2013, MicroED established a demonstrated ability for solving structures of difficult samples using vanishingly small crystals. However, membrane proteins remain the next big frontier for MicroED. The intrinsic properties of membrane proteins necessitate improved sample handling and imaging techniques to be developed and optimized for MicroED. Here, we summarize the milestones of electron crystallography of two-dimensional crystals leading to MicroED of three-dimensional crystals. Then, we focus on four different membrane protein families and discuss representatives from each family solved by MicroED. Portland Press Ltd. 2022-02-28 2022-02-22 /pmc/articles/PMC9022970/ /pubmed/35191473 http://dx.doi.org/10.1042/BST20210911 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Articles
Gallenito, Marc J.
Gonen, Tamir
Studying membrane proteins with MicroED
title Studying membrane proteins with MicroED
title_full Studying membrane proteins with MicroED
title_fullStr Studying membrane proteins with MicroED
title_full_unstemmed Studying membrane proteins with MicroED
title_short Studying membrane proteins with MicroED
title_sort studying membrane proteins with microed
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9022970/
https://www.ncbi.nlm.nih.gov/pubmed/35191473
http://dx.doi.org/10.1042/BST20210911
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