Cover Picture: Effect of Ganglioside GM3 Synthase Gene Knockout on the Glycoprotein N‐Glycan Profile of Mouse Embryonic Fibroblast (ChemBioChem 1/2013). Issue 1 (23rd December 2012)
- Record Type:
- Journal Article
- Title:
- Cover Picture: Effect of Ganglioside GM3 Synthase Gene Knockout on the Glycoprotein N‐Glycan Profile of Mouse Embryonic Fibroblast (ChemBioChem 1/2013). Issue 1 (23rd December 2012)
- Main Title:
- Cover Picture: Effect of Ganglioside GM3 Synthase Gene Knockout on the Glycoprotein N‐Glycan Profile of Mouse Embryonic Fibroblast (ChemBioChem 1/2013)
- Authors:
- Nagahori, Noriko
Yamashita, Tadashi
Amano, Maho
Nishimura, Shin‐Ichiro - Abstract:
- <abstract abstract-type="graphical" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p> <bold>The cover picture shows</bold> that gene knockout of the enzymes responsible for glycosphingolipid (GSL) synthesis significantly influences the biosynthesis of glycoprotein <italic>N</italic>‐glycans. On <ext-link ext-link-type="doi" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">p. 73 ff., </ext-link> S.‐I. Nishimura et al. describe how they have established a general and comprehensive glycomics protocol of cellular GLSs and <italic>N</italic>‐glycans of glycoproteins. To test the feasibility of a glycoblotting‐based protocol, whole glycans released both from GLSs and glycoproteins were profiled concurrently by using the GM3 synthase‐deficient mouse embryonic fibroblast GM3(−/−). GM3(−/−) cells did not synthesize GM3 or any downstream product of GM3 synthase. Instead, expression levels of o‐series gangliosides involving GM1b and GD1‐α were increased dramatically whereas a‐/b‐series gangliosides were predominantly detected in wild‐type cells. It was also discovered that glycoprotein N‐glycan profiles of GM3(−/−) cells are significantly different from those of WT cells, though GM3 synthase is responsible only for GSL synthesis and is not associated with glycoprotein <italic>N</italic>‐glycan biosynthesis.<boxed-text content-type="graphic" position="anchor" orientation="portrait"><graphic position="anchor" mimetype="image"<abstract abstract-type="graphical" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p> <bold>The cover picture shows</bold> that gene knockout of the enzymes responsible for glycosphingolipid (GSL) synthesis significantly influences the biosynthesis of glycoprotein <italic>N</italic>‐glycans. On <ext-link ext-link-type="doi" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">p. 73 ff., </ext-link> S.‐I. Nishimura et al. describe how they have established a general and comprehensive glycomics protocol of cellular GLSs and <italic>N</italic>‐glycans of glycoproteins. To test the feasibility of a glycoblotting‐based protocol, whole glycans released both from GLSs and glycoproteins were profiled concurrently by using the GM3 synthase‐deficient mouse embryonic fibroblast GM3(−/−). GM3(−/−) cells did not synthesize GM3 or any downstream product of GM3 synthase. Instead, expression levels of o‐series gangliosides involving GM1b and GD1‐α were increased dramatically whereas a‐/b‐series gangliosides were predominantly detected in wild‐type cells. It was also discovered that glycoprotein N‐glycan profiles of GM3(−/−) cells are significantly different from those of WT cells, though GM3 synthase is responsible only for GSL synthesis and is not associated with glycoprotein <italic>N</italic>‐glycan biosynthesis.<boxed-text content-type="graphic" position="anchor" orientation="portrait"><graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pgg1p96pjcb" orientation="portrait" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" /></boxed-text></p> </abstract> … (more)
- Is Part Of:
- Chembiochem. Volume 14:Issue 1(2013)
- Journal:
- Chembiochem
- Issue:
- Volume 14:Issue 1(2013)
- Issue Display:
- Volume 14, Issue 1 (2013)
- Year:
- 2013
- Volume:
- 14
- Issue:
- 1
- Issue Sort Value:
- 2013-0014-0001-0000
- Page Start:
- 1
- Page End:
- 1
- Publication Date:
- 2012-12-23
- Subjects:
- Biochemistry -- Periodicals
Molecular biology -- Periodicals
Pharmaceutical chemistry -- Periodicals
572 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1439-7633 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/cbic.201290078 ↗
- Languages:
- English
- ISSNs:
- 1439-4227
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3133.490980
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4346.xml