Literature DB >> 15939591

The glycan code of the endoplasmic reticulum: asparagine-linked carbohydrates as protein maturation and quality-control tags.

Daniel N Hebert1, Scott C Garman, Maurizio Molinari.   

Abstract

The majority of proteins that traverse the secretory pathway receive asparagine (Asn)-linked glycosylations. Glycans are bulky hydrophilic modifications that serve a variety of structural and functional roles within the cell. Here, we review the recent growing knowledge on the role of Asn-linked glycans as maturation and quality-control protein tags in the early secretory pathway. The carbohydrate composition encodes crucial information about the structure, localization and age of glycoproteins. The "glycan code" is encoded by a series of glycosidases and carbohydrate transferases that line the secretory pathway. This code is deciphered by carbohydrate-binding proteins that possess distinct carbohydrate binding properties and act as molecular chaperones or sorting receptors. These glycosidases and transferases work in concert with resident secretory pathway carbohydrate-binding proteins to form a network that assists in the maturation and trafficking of both native and aberrant glycoproteins within the cell.

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Year:  2005        PMID: 15939591     DOI: 10.1016/j.tcb.2005.05.007

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  83 in total

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3.  Analysis of site-specific N-glycan remodeling in the endoplasmic reticulum and the Golgi.

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Review 4.  The protective and destructive roles played by molecular chaperones during ERAD (endoplasmic-reticulum-associated degradation).

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6.  Adapter-mediated substrate selection for endoplasmic reticulum-associated degradation.

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8.  Redundant and Antagonistic Roles of XTP3B and OS9 in Decoding Glycan and Non-glycan Degrons in ER-Associated Degradation.

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Review 9.  Role of unusual O-glycans in intercellular signaling.

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10.  Regulation of G-protein coupled receptor traffic by an evolutionary conserved hydrophobic signal.

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