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Cryo‐electron microscopy of cholinesterases, present and future

Acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) exist in a variety of oligomeric forms, each with defined cellular and subcellular distributions. Although crystal structures of AChE and BChE have been available for many years, structures of the physiologically relevant ChE tetramer were...

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Autores principales: Leung, Miguel Ricardo, Zeev‐Ben‐Mordehai, Tzviya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518539/
https://www.ncbi.nlm.nih.gov/pubmed/33222205
http://dx.doi.org/10.1111/jnc.15245
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author Leung, Miguel Ricardo
Zeev‐Ben‐Mordehai, Tzviya
author_facet Leung, Miguel Ricardo
Zeev‐Ben‐Mordehai, Tzviya
author_sort Leung, Miguel Ricardo
collection PubMed
description Acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) exist in a variety of oligomeric forms, each with defined cellular and subcellular distributions. Although crystal structures of AChE and BChE have been available for many years, structures of the physiologically relevant ChE tetramer were only recently solved by cryo‐electron microscopy (cryo‐EM) single‐particle analysis. Here, we briefly review how these structures contribute to our understanding of cholinesterase oligomerization, highlighting the advantages of using cryo‐EM to resolve structures of protein assemblies that cannot be expressed recombinantly. We argue that the next frontier in cholinesterase structural biology is to image membrane‐anchored ChE oligomers directly in their native environment—the cell. [Image: see text]
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spelling pubmed-85185392021-10-21 Cryo‐electron microscopy of cholinesterases, present and future Leung, Miguel Ricardo Zeev‐Ben‐Mordehai, Tzviya J Neurochem Reviews Acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) exist in a variety of oligomeric forms, each with defined cellular and subcellular distributions. Although crystal structures of AChE and BChE have been available for many years, structures of the physiologically relevant ChE tetramer were only recently solved by cryo‐electron microscopy (cryo‐EM) single‐particle analysis. Here, we briefly review how these structures contribute to our understanding of cholinesterase oligomerization, highlighting the advantages of using cryo‐EM to resolve structures of protein assemblies that cannot be expressed recombinantly. We argue that the next frontier in cholinesterase structural biology is to image membrane‐anchored ChE oligomers directly in their native environment—the cell. [Image: see text] John Wiley and Sons Inc. 2020-12-10 2021-09 /pmc/articles/PMC8518539/ /pubmed/33222205 http://dx.doi.org/10.1111/jnc.15245 Text en © 2020 The Authors. Journal of Neurochemistry published by John Wiley & Sons Ltd on behalf of International Society for Neurochemistry https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Leung, Miguel Ricardo
Zeev‐Ben‐Mordehai, Tzviya
Cryo‐electron microscopy of cholinesterases, present and future
title Cryo‐electron microscopy of cholinesterases, present and future
title_full Cryo‐electron microscopy of cholinesterases, present and future
title_fullStr Cryo‐electron microscopy of cholinesterases, present and future
title_full_unstemmed Cryo‐electron microscopy of cholinesterases, present and future
title_short Cryo‐electron microscopy of cholinesterases, present and future
title_sort cryo‐electron microscopy of cholinesterases, present and future
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518539/
https://www.ncbi.nlm.nih.gov/pubmed/33222205
http://dx.doi.org/10.1111/jnc.15245
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