Skip Navigation

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (48)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Kmiécik, D.
Right arrow Articles by Cacan, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kmiécik, D.
Right arrow Articles by Cacan, R.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Glycobiology vol 5 no 5 pp. 483-494, 1995
© 1995


research-article

Catabolism of glycan moieties of lipid intermediates leads to a single Man5GlcNAc oligosaccharide isomer: a study with permeabilized CHO cells

Daniel Kmiécik, Virginie Herman, Corné J.M. Stroop, Jean-Claude Michalski, Anne-Marie Mir, Odette Labiau, André Verbert1 and René Cacan

Laboratoire de Chimie Biologique, UMR N°111 du CNRS, Université des Sciences et Technologies de Lille 59655 Villeneuve d'Ascq cedex, France


1To whom correspondence should be addressed

Received on December 5, 1994; revised on April 6, 1995; accepted on April 10, 1995

This paper presents kinetic and structural analyses of oligosaccharide material released during glycosylation in permeabilized Chinese hamster ovary cells incubated with sugar nucleotides. Permeabilized cells released 30 times more oligosaccharide material than metabolically labelled cells, normalized to the amount of labelled glycoprotein acceptor, making this an amenable system for study. Fifteen to forty per cent of the oligosaccharide material released by permeabilized cells was oligosaccharide-phosphate, depending on the nature and amount of the oligosaccharide-lipids synthesized. The oligosaccharide-phosphates released were recovered in the cytosol, and were exclusively Man2GlcNAc2P and Man5GlcNAc2P, released from oligosaccharide-lipids thought to be facing the cytosol. In contrast, the structures found as neutral oligosaccharide material were similar to those attached to newly synthesized glycoproteins, indicating that the oligosaccharides were subjected to the same processing enzymes whether or not they were protein bound. Importantly, the kinetics of the transfer to protein and the release of free neutral oligosaccharide were parallel, suggesting that the same enzyme was responsible for both processes. Structural analyses demonstrated that the same Man5GlcNAc2 structure was transferred to protein and released as free oligosaccharide. Neutral oligosaccharides were found in both the cytosol and the pellet; however, oligosaccharides with one GlcNAc residue at the reducing end (OS-Gn1) were found exclusively in the supemate. The major neutral oligosaccharide produced after 2 h of metabolic labelling was Man5GlcNAc and it was found in the cytosol.

lipid intermediates oligomannoside-phosphates permeabilized cells subcellular distribution of oligomannosides


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
H. Nothaft, X. Liu, D. J. McNally, J. Li, and C. M. Szymanski
Study of free oligosaccharides derived from the bacterial N-glycosylation pathway
PNAS, September 1, 2009; 106(35): 15019 - 15024.
[Abstract] [Full Text] [PDF]


Home page
GlycobiologyHome page
W. Vleugels, L. Keldermans, J. Jaeken, T. D Butters, J.-C. Michalski, G. Matthijs, and F. Foulquier
Quality control of glycoproteins bearing truncated glycans in an ALG9-defective (CDG-IL) patient
Glycobiology, August 1, 2009; 19(8): 910 - 917.
[Abstract] [Full Text] [PDF]


Home page
GlycobiologyHome page
E. Kuokkanen, W. Smith, M. Makinen, H. Tuominen, M. Puhka, E. Jokitalo, S. Duvet, T. Berg, and P. Heikinheimo
Characterization and subcellular localization of human neutral class II{alpha}-mannosidase cytosolic enzymes/free oligosaccharides/glycosidehydrolase family 38/M2C1/N-glycosylation
Glycobiology, October 1, 2007; 17(10): 1084 - 1093.
[Abstract] [Full Text] [PDF]


Home page
J BiochemHome page
K. Moriguchi, T. Takemoto, T. Aoki, S.-i. Nakakita, S. Natsuka, and S. Hase
Free Oligosaccharides with Lewis x Structure Expressed in the Segmentation Period of Zebrafish Embryo
J. Biochem., August 1, 2007; 142(2): 213 - 227.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
T. Kato, K. Kitamura, M. Maeda, Y. Kimura, T. Katayama, H. Ashida, and K. Yamamoto
Free Oligosaccharides in the Cytosol of Caenorhabditis elegans Are Generated through Endoplasmic Reticulum-Golgi Trafficking
J. Biol. Chem., July 27, 2007; 282(30): 22080 - 22088.
[Abstract] [Full Text] [PDF]


Home page
GlycobiologyHome page
K. Yanagida, S. Natsuka, and S. Hase
Structural diversity of cytosolic free oligosaccharides in the human hepatoma cell line, HepG2
Glycobiology, April 1, 2006; 16(4): 294 - 304.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
A. Op De Beeck, Y. Rouille, M. Caron, S. Duvet, and J. Dubuisson
The Transmembrane Domains of the prM and E Proteins of Yellow Fever Virus Are Endoplasmic Reticulum Localization Signals
J. Virol., November 15, 2004; 78(22): 12591 - 12602.
[Abstract] [Full Text] [PDF]


Home page
GlycobiologyHome page
S. Duvet, F. Foulquier, A.-M. Mir, F. Chirat, and R. Cacan
Discrimination between lumenal and cytosolic sites of deglycosylation in endoplasmic reticulum-associated degradation of glycoproteins by using benzyl mannose in CHO cell lines
Glycobiology, September 1, 2004; 14(9): 841 - 849.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
T. Suzuki, K. Yano, S. Sugimoto, K. Kitajima, W. J. Lennarz, S. Inoue, Y. Inoue, and Y. Emori
Endo-beta -N-acetylglucosaminidase, an enzyme involved in processing of free oligosaccharides in the cytosol
PNAS, July 23, 2002; 99(15): 9691 - 9696.
[Abstract] [Full Text] [PDF]


Home page
GlycobiologyHome page
M. Ermonval, C. Kitzmuller, A. M. Mir, R. Cacan, and N. E. Ivessa
N-glycan structure of a short-lived variant of ribophorin I expressed in the MadIA214 glycosylation-defective cell line reveals the role of a mannosidase that is not ER mannosidase I in the process of glycoprotein degradation
Glycobiology, July 1, 2001; 11(7): 565 - 576.
[Abstract] [Full Text] [PDF]


Home page
GlycobiologyHome page
R. Cacan and A. Verbert
Transport of free and N-linked oligomannoside species across the rough endoplasmic reticulum membranes
Glycobiology, July 1, 2000; 10(7): 645 - 648.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
D. J. Moloney, L. H. Shair, F. M. Lu, J. Xia, R. Locke, K. L. Matta, and R. S. Haltiwanger
Mammalian Notch1 Is Modified with Two Unusual Forms of O-Linked Glycosylation Found on Epidermal Growth Factor-like Modules
J. Biol. Chem., March 24, 2000; 275(13): 9604 - 9611.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
L. Cocquerel, S. Duvet, J.-C. Meunier, A. Pillez, R. Cacan, C. Wychowski, and J. Dubuisson
The Transmembrane Domain of Hepatitis C Virus Glycoprotein E1 Is a Signal for Static Retention in the Endoplasmic Reticulum
J. Virol., April 1, 1999; 73(4): 2641 - 2649.
[Abstract] [Full Text]


Home page
J. Biol. Chem.Home page
S. Duvet, L. Cocquerel, A. Pillez, R. Cacan, A. Verbert, D. Moradpour, C. Wychowski, and J. Dubuisson
Hepatitis C Virus Glycoprotein Complex Localization in the Endoplasmic Reticulum Involves a Determinant for Retention and Not Retrieval
J. Biol. Chem., November 27, 1998; 273(48): 32088 - 32095.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
T. Suzuki, Q. Yan, and W. J. Lennarz
Complex, Two-way Traffic of Molecules Across the Membrane of the Endoplasmic Reticulum
J. Biol. Chem., April 24, 1998; 273(17): 10083 - 10086.
[Full Text] [PDF]


Home page
JCBHome page
A. Saint-Pol, C. Bauvy, P. Codogno, and S. E.H. Moore
Transfer of Free Polymannose-type Oligosaccharides from the Cytosol to Lysosomes in Cultured Human Hepatocellular Carcinoma HEPG2 Cells
J. Cell Biol., January 13, 1997; 136(1): 45 - 59.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
M Ermonval, R Cacan, K Gorgas, I. Haas, A Verbert, and G Buttin
Differential fate of glycoproteins carrying a monoglucosylated form of truncated N-glycan in a new CHO line, MadIA214214, selected for a thermosensitive secretory defect
J. Cell Sci., January 2, 1997; 110(3): 323 - 336.
[Abstract] [PDF]


Home page
J. Biol. Chem.Home page
A. Op De Beeck, R. Montserret, S. Duvet, L. Cocquerel, R. Cacan, B. Barberot, M. Le Maire, F. Penin, and J. Dubuisson
The Transmembrane Domains of Hepatitis C Virus Envelope Glycoproteins E1 and E2 Play a Major Role in Heterodimerization
J. Biol. Chem., September 29, 2000; 275(40): 31428 - 31437.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
R. Cacan, S. Duvet, O. Labiau, A. Verbert, and S. S. Krag
Monoglucosylated Oligomannosides Are Released during the Degradation Process of Newly Synthesized Glycoproteins
J. Biol. Chem., June 15, 2001; 276(25): 22307 - 22312.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.