Cryo-electron microscopy of cholinesterases, present and future

Publication date

2021-09

Authors

Leung, Miguel RicardoISNI 0000000492906538
Zeev-Ben-Mordehai, TzviyaISNI 0000000492962767

Editors

Advisors

Supervisors

Document Type

Article
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License

cc_by

Abstract

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. (Figure presented.).

Keywords

cholinesterase, cryo-electron microscopy, cryo-electron tomography, Biochemistry, Cellular and Molecular Neuroscience

Citation

Leung, M R & Zeev-Ben-Mordehai, T 2021, 'Cryo-electron microscopy of cholinesterases, present and future', Journal of Neurochemistry, vol. 158, no. 6, pp. 1236-1243. https://doi.org/10.1111/jnc.15245