Studying the organization of the Golgi by super-resolution microscopy

The Golgi complex is essential for protein transport and posttranslational modification in mammalian cells. It is critical to know the cisternal distribution of Golgi proteins to understand Golgi functions. The cis-to-trans or axial localization of a Golgi protein can be obtained using our previousl...

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Main Authors: Tie, Hieng Chiong, Lu, Lei
Other Authors: School of Biological Sciences
Format: Article
Language:English
Published: 2023
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Online Access:https://hdl.handle.net/10356/164099
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1640992023-02-28T17:11:07Z Studying the organization of the Golgi by super-resolution microscopy Tie, Hieng Chiong Lu, Lei School of Biological Sciences Science::Biological sciences::Cytology Golgi Complex Golgi Cisternae The Golgi complex is essential for protein transport and posttranslational modification in mammalian cells. It is critical to know the cisternal distribution of Golgi proteins to understand Golgi functions. The cis-to-trans or axial localization of a Golgi protein can be obtained using our previously developed method, Golgi protein localization by imaging centers of mass (GLIM), in nocodazole-induced Golgi ministacks (hereafter referred to as ministacks). However, there is no effective light microscopic method to reveal the lateral localization of a Golgi protein, which is the distribution within the Golgi cisternae. The challenge is partially caused by the random orientations and the tight congregation of Golgi stacks at the perinuclear region. Here, we summarize our method to identify en face and side views of ministacks. It takes advantage of the characteristic ring and double-punctum staining patterns exhibited by cisternal rim-localized proteins. After averaging multiple en face views, the resulting image reveals the intrinsic organization of cisternae in a non-biased manner. Ministry of Education (MOE) Submitted/Accepted version This work was supported by the following grants to L.L.: Tier2 MOE2018-T2-2-026. 2023-01-06T02:20:07Z 2023-01-06T02:20:07Z 2023 Journal Article Tie, H. C. & Lu, L. (2023). Studying the organization of the Golgi by super-resolution microscopy. Methods in Molecular Biology, 2557, 113-126. https://dx.doi.org/10.1007/978-1-0716-2639-9_9 978-1-0716-2638-2 978-1-0716-2639-9 1064-3745 https://hdl.handle.net/10356/164099 10.1007/978-1-0716-2639-9_9 2557 2-s2.0-85144233944 2557 113 126 en MOE2018-T2-2-026 Methods in Molecular Biology © 2023 The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature. All rights reserved. This version of the article has been accepted for publication, after peer review and is subject to Springer Nature’s AM terms of use, but is not the Version of Record and does not reflect post-acceptance improvements, or any corrections. The Version of Record is available online at: http://dx.doi.org/10.1007/978-1-0716-2639-9_9. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Science::Biological sciences::Cytology
Golgi Complex
Golgi Cisternae
spellingShingle Science::Biological sciences::Cytology
Golgi Complex
Golgi Cisternae
Tie, Hieng Chiong
Lu, Lei
Studying the organization of the Golgi by super-resolution microscopy
description The Golgi complex is essential for protein transport and posttranslational modification in mammalian cells. It is critical to know the cisternal distribution of Golgi proteins to understand Golgi functions. The cis-to-trans or axial localization of a Golgi protein can be obtained using our previously developed method, Golgi protein localization by imaging centers of mass (GLIM), in nocodazole-induced Golgi ministacks (hereafter referred to as ministacks). However, there is no effective light microscopic method to reveal the lateral localization of a Golgi protein, which is the distribution within the Golgi cisternae. The challenge is partially caused by the random orientations and the tight congregation of Golgi stacks at the perinuclear region. Here, we summarize our method to identify en face and side views of ministacks. It takes advantage of the characteristic ring and double-punctum staining patterns exhibited by cisternal rim-localized proteins. After averaging multiple en face views, the resulting image reveals the intrinsic organization of cisternae in a non-biased manner.
author2 School of Biological Sciences
author_facet School of Biological Sciences
Tie, Hieng Chiong
Lu, Lei
format Article
author Tie, Hieng Chiong
Lu, Lei
author_sort Tie, Hieng Chiong
title Studying the organization of the Golgi by super-resolution microscopy
title_short Studying the organization of the Golgi by super-resolution microscopy
title_full Studying the organization of the Golgi by super-resolution microscopy
title_fullStr Studying the organization of the Golgi by super-resolution microscopy
title_full_unstemmed Studying the organization of the Golgi by super-resolution microscopy
title_sort studying the organization of the golgi by super-resolution microscopy
publishDate 2023
url https://hdl.handle.net/10356/164099
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