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Investigating eukaryotic cells with cryo-ET

The interior of eukaryotic cells is mysterious. How do the large communities of macromolecular machines interact with each other? How do the structures and positions of these nanoscopic entities respond to new stimuli? Questions like these can now be answered with the help of a method called electro...

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Detalles Bibliográficos
Autores principales: Ng, Cai Tong, Gan, Lu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6960407/
https://www.ncbi.nlm.nih.gov/pubmed/31935172
http://dx.doi.org/10.1091/mbc.E18-05-0329
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author Ng, Cai Tong
Gan, Lu
author_facet Ng, Cai Tong
Gan, Lu
author_sort Ng, Cai Tong
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description The interior of eukaryotic cells is mysterious. How do the large communities of macromolecular machines interact with each other? How do the structures and positions of these nanoscopic entities respond to new stimuli? Questions like these can now be answered with the help of a method called electron cryotomography (cryo-ET). Cryo-ET will ultimately reveal the inner workings of a cell at the protein, secondary structure, and perhaps even side-chain levels. Combined with genetic or pharmacological perturbation, cryo-ET will allow us to answer previously unimaginable questions, such as how structure, biochemistry, and forces are related in situ. Because it bridges structural biology and cell biology, cryo-ET is indispensable for structural cell biology—the study of the 3-D macromolecular structure of cells. Here we discuss some of the key ideas, strategies, auxiliary techniques, and innovations that an aspiring structural cell biologist will consider when planning to ask bold questions.
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spelling pubmed-69604072020-03-30 Investigating eukaryotic cells with cryo-ET Ng, Cai Tong Gan, Lu Mol Biol Cell Perspective The interior of eukaryotic cells is mysterious. How do the large communities of macromolecular machines interact with each other? How do the structures and positions of these nanoscopic entities respond to new stimuli? Questions like these can now be answered with the help of a method called electron cryotomography (cryo-ET). Cryo-ET will ultimately reveal the inner workings of a cell at the protein, secondary structure, and perhaps even side-chain levels. Combined with genetic or pharmacological perturbation, cryo-ET will allow us to answer previously unimaginable questions, such as how structure, biochemistry, and forces are related in situ. Because it bridges structural biology and cell biology, cryo-ET is indispensable for structural cell biology—the study of the 3-D macromolecular structure of cells. Here we discuss some of the key ideas, strategies, auxiliary techniques, and innovations that an aspiring structural cell biologist will consider when planning to ask bold questions. The American Society for Cell Biology 2020-01-15 /pmc/articles/PMC6960407/ /pubmed/31935172 http://dx.doi.org/10.1091/mbc.E18-05-0329 Text en © 2020 Ng and Gan. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0 This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License.
spellingShingle Perspective
Ng, Cai Tong
Gan, Lu
Investigating eukaryotic cells with cryo-ET
title Investigating eukaryotic cells with cryo-ET
title_full Investigating eukaryotic cells with cryo-ET
title_fullStr Investigating eukaryotic cells with cryo-ET
title_full_unstemmed Investigating eukaryotic cells with cryo-ET
title_short Investigating eukaryotic cells with cryo-ET
title_sort investigating eukaryotic cells with cryo-et
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6960407/
https://www.ncbi.nlm.nih.gov/pubmed/31935172
http://dx.doi.org/10.1091/mbc.E18-05-0329
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