Protocol for analyzing the biosynthesis and degradation of N-glycan precursors in mammalian cells

Summary: N-glycosylation is a fundamental post-translational protein modification in the endoplasmic reticulum of eukaryotic cells. The biosynthetic and catabolic flux of N-glycans in eukaryotic cells has long been analyzed by metabolic labeling using radiolabeled sugars. Here, we introduce a non-ra...

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Main Authors: Yoichiro Harada, Kazuki Nakajima, Shengtao Li, Tadashi Suzuki, Naoyuki Taniguchi
Format: Article
Language:English
Published: Elsevier 2021-03-01
Series:STAR Protocols
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S266616672100023X
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spelling doaj-ae5b4d72fb954832ba71d8ebb4a0d32d2021-03-22T12:53:11ZengElsevierSTAR Protocols2666-16672021-03-0121100316Protocol for analyzing the biosynthesis and degradation of N-glycan precursors in mammalian cellsYoichiro Harada0Kazuki Nakajima1Shengtao Li2Tadashi Suzuki3Naoyuki Taniguchi4Department of Glyco-Oncology and Medical Biochemistry, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-ku, Osaka 541-8567, Japan; Corresponding authorCenter for Joint Research Facilities Support, Research Promotion and Support Headquarters, Fujita Health University, Toyoake, Aichi 470-1192, JapanGlycometabolic Biochemistry Laboratory, RIKEN Cluster for Pioneering Research, Saitama 351-0198, JapanGlycometabolic Biochemistry Laboratory, RIKEN Cluster for Pioneering Research, Saitama 351-0198, JapanDepartment of Glyco-Oncology and Medical Biochemistry, Osaka International Cancer Institute, 3-1-69 Otemae, Chuo-ku, Osaka 541-8567, JapanSummary: N-glycosylation is a fundamental post-translational protein modification in the endoplasmic reticulum of eukaryotic cells. The biosynthetic and catabolic flux of N-glycans in eukaryotic cells has long been analyzed by metabolic labeling using radiolabeled sugars. Here, we introduce a non-radiolabeling protocol for the isolation, structural determination, and quantification of N-glycan precursors, dolichol-linked oligosaccharides, and the related metabolites, including phosphorylated oligosaccharides and nucleotide sugars. Our protocol allows for capturing of the biosynthesis and degradation of N-glycan precursors at steady state.For complete details on the use and execution of this protocol, please refer to Harada et al. (2013), Harada et al. (2020), and Nakajima et al. (2013).http://www.sciencedirect.com/science/article/pii/S266616672100023XCell biologyMetabolismProtein biochemistryProtein expression and purificationMass spectrometry
collection DOAJ
language English
format Article
sources DOAJ
author Yoichiro Harada
Kazuki Nakajima
Shengtao Li
Tadashi Suzuki
Naoyuki Taniguchi
spellingShingle Yoichiro Harada
Kazuki Nakajima
Shengtao Li
Tadashi Suzuki
Naoyuki Taniguchi
Protocol for analyzing the biosynthesis and degradation of N-glycan precursors in mammalian cells
STAR Protocols
Cell biology
Metabolism
Protein biochemistry
Protein expression and purification
Mass spectrometry
author_facet Yoichiro Harada
Kazuki Nakajima
Shengtao Li
Tadashi Suzuki
Naoyuki Taniguchi
author_sort Yoichiro Harada
title Protocol for analyzing the biosynthesis and degradation of N-glycan precursors in mammalian cells
title_short Protocol for analyzing the biosynthesis and degradation of N-glycan precursors in mammalian cells
title_full Protocol for analyzing the biosynthesis and degradation of N-glycan precursors in mammalian cells
title_fullStr Protocol for analyzing the biosynthesis and degradation of N-glycan precursors in mammalian cells
title_full_unstemmed Protocol for analyzing the biosynthesis and degradation of N-glycan precursors in mammalian cells
title_sort protocol for analyzing the biosynthesis and degradation of n-glycan precursors in mammalian cells
publisher Elsevier
series STAR Protocols
issn 2666-1667
publishDate 2021-03-01
description Summary: N-glycosylation is a fundamental post-translational protein modification in the endoplasmic reticulum of eukaryotic cells. The biosynthetic and catabolic flux of N-glycans in eukaryotic cells has long been analyzed by metabolic labeling using radiolabeled sugars. Here, we introduce a non-radiolabeling protocol for the isolation, structural determination, and quantification of N-glycan precursors, dolichol-linked oligosaccharides, and the related metabolites, including phosphorylated oligosaccharides and nucleotide sugars. Our protocol allows for capturing of the biosynthesis and degradation of N-glycan precursors at steady state.For complete details on the use and execution of this protocol, please refer to Harada et al. (2013), Harada et al. (2020), and Nakajima et al. (2013).
topic Cell biology
Metabolism
Protein biochemistry
Protein expression and purification
Mass spectrometry
url http://www.sciencedirect.com/science/article/pii/S266616672100023X
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