Literature DB >> 19016451

Endoglycosidase and glycoamidase release of N-linked glycans.

Hudson H Freeze1, Christian Kranz.   

Abstract

Nearly all proteins entering the lumen of the endoplasmic reticulum (ER) become glycosylated en route to a cellular organelle, the plasma membrane, or the extracellular space. Many glycans can be attached to proteins, but the most common are the N-linked glycans (oligosaccharides). These chains are added very soon after a protein enters the ER, but they undergo extensive remodeling (processing), especially in the Golgi. Processing changes the sensitivity of the N-glycan to enzymes that cleave entire sugar chains or individual monosaccharides, which also changes the migration of the protein on SDS gels. These changes can be used to indicate when a protein has passed a particular subcellular location. This unit details some of the methods used to track a protein as it traffics from the ER to the Golgi toward its final location.

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Year:  2008        PMID: 19016451     DOI: 10.1002/0471142735.im0815s83

Source DB:  PubMed          Journal:  Curr Protoc Immunol        ISSN: 1934-3671


  7 in total

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7.  The cargo receptor SURF4 promotes the efficient cellular secretion of PCSK9.

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  7 in total

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