Literature DB >> 1478359

Physiological relevance of protein glycosylation.

D A Cumming1.   

Abstract

The glycosylation of proteins is a complex biological pathway which is ordered and non-random. It is also a deterministic pathway dependent upon protein sequence, cellular phenotype, and the physiological environment. Two principal physiological roles have emerged within the past decade for protein-linked glycans: as recognition determinants and as modulators of various protein attributes such as bioactivity, pharmacokinetics, folding, and immunogenicity. All these attributes are crucial to development and application of protein-based pharmaceuticals. However, protein glycosylation represents a difficult structure/function problem since most glycoproteins exhibit microheterogeneity and oligosaccharides frequently contribute to this heterogeneity. Nevertheless, recent data suggest that different members of the heterogeneous ensemble exhibit distinguishable intrinsic properties, suggesting that the microheterogeneity of protein glycosylation represents a sophisticated mechanism of biological control.

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Year:  1992        PMID: 1478359

Source DB:  PubMed          Journal:  Dev Biol Stand        ISSN: 0301-5149


  4 in total

1.  Structure and function of the N-linked glycans of HBP/CAP37/azurocidin: crystal structure determination and biological characterization of nonglycosylated HBP.

Authors:  L F Iversen; J S Kastrup; S E Bjørn; F C Wiberg; I K Larsen; H J Flodgaard; P B Rasmussen
Journal:  Protein Sci       Date:  1999-10       Impact factor: 6.725

2.  DMP1-CDG (CDG1e) with Significant Gastrointestinal Manifestations; Phenotype and Genotype Expansion.

Authors:  C Bursle; D Brown; J Cardinal; F Connor; S Calvert; D Coman
Journal:  JIMD Rep       Date:  2016-08-02

3.  Comparison of N-Glycan Pattern of Recombinant Human Coagulation Factors II and IX Expressed in Chinese Hamster Ovary (CHO) and African Green Monkey (Vero) Cells.

Authors: 
Journal:  J Thromb Thrombolysis       Date:  1996       Impact factor: 2.300

4.  Insertion into Aspergillus nidulans of functional UDP-GlcNAc: alpha 3-D- mannoside beta-1,2-N-acetylglucosaminyl-transferase I, the enzyme catalysing the first committed step from oligomannose to hybrid and complex N-glycans.

Authors:  I Kalsner; W Hintz; L S Reid; H Schachter
Journal:  Glycoconj J       Date:  1995-06       Impact factor: 2.916

  4 in total

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