Literature DB >> 29043680

Analysis of Protein Glycosylation in the ER.

Jennifer Schoberer1, Yun-Ji Shin1, Ulrike Vavra1, Christiane Veit1, Richard Strasser2.   

Abstract

Protein N-glycosylation is an essential posttranslational modification which is initiated in the endoplasmic reticulum. In plants, the N-glycans play a pivotal role for protein folding and quality control. Through the interaction of glycan processing and binding reactions mediated by ER-resident glycosidases and specific carbohydrate binding proteins, the N-glycans contribute to the adoption of a native protein conformation. Properly folded glycoproteins are released from these processes and allowed to continue their transit to the Golgi where further processing and maturation of N-glycans leads to the formation of more complex structures with different functions. Incompletely folded glycoproteins are removed from the ER by a highly conserved degradation process to prevent the accumulation or secretion of misfolded proteins and maintain ER homeostasis. Here, we describe methods to analyze the N-glycosylation status and the glycan-dependent ER-associated degradation process in plants.

Entities:  

Keywords:  ERAD; Glycoprotein; N-glycosylation; Oligosaccharyltransferase; Quality control

Mesh:

Substances:

Year:  2018        PMID: 29043680      PMCID: PMC7039702          DOI: 10.1007/978-1-4939-7389-7_16

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  42 in total

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Journal:  Methods Mol Biol       Date:  2015

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Journal:  Gene       Date:  1997-10-24       Impact factor: 3.688

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Review 4.  N-linked glycosylation and homeostasis of the endoplasmic reticulum.

Authors:  Natalia Cherepanova; Shiteshu Shrimal; Reid Gilmore
Journal:  Curr Opin Cell Biol       Date:  2016-04-14       Impact factor: 8.382

Review 5.  An evolving view of the eukaryotic oligosaccharyltransferase.

Authors:  Daniel J Kelleher; Reid Gilmore
Journal:  Glycobiology       Date:  2005-11-29       Impact factor: 4.313

6.  The STT3a subunit isoform of the Arabidopsis oligosaccharyltransferase controls adaptive responses to salt/osmotic stress.

Authors:  Hisashi Koiwa; Fang Li; Michael G McCully; Imelda Mendoza; Nozomu Koizumi; Yuzuki Manabe; Yuko Nakagawa; Jianhua Zhu; Ana Rus; José M Pardo; Ray A Bressan; Paul M Hasegawa
Journal:  Plant Cell       Date:  2003-09-05       Impact factor: 11.277

Review 7.  N-linked protein glycosylation in the ER.

Authors:  Markus Aebi
Journal:  Biochim Biophys Acta       Date:  2013-04-10

8.  Allele-specific suppression of a defective brassinosteroid receptor reveals a physiological role of UGGT in ER quality control.

Authors:  Hua Jin; Zhenyan Yan; Kyoung Hee Nam; Jianming Li
Journal:  Mol Cell       Date:  2007-06-22       Impact factor: 17.970

9.  A context-independent N-glycan signal targets the misfolded extracellular domain of Arabidopsis STRUBBELIG to endoplasmic-reticulum-associated degradation.

Authors:  Silvia Hüttner; Christiane Veit; Ulrike Vavra; Jennifer Schoberer; Martina Dicker; Daniel Maresch; Friedrich Altmann; Richard Strasser
Journal:  Biochem J       Date:  2014-12-15       Impact factor: 3.857

10.  A subunit of the oligosaccharyltransferase complex is required for interspecific gametophyte recognition in Arabidopsis.

Authors:  Lena M Müller; Heike Lindner; Nuno D Pires; Valeria Gagliardini; Ueli Grossniklaus
Journal:  Nat Commun       Date:  2016-03-11       Impact factor: 14.919

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3.  The Major Peanut Allergen Ara h 2 Produced in Nicotiana benthamiana Contains Hydroxyprolines and Is a Viable Alternative to the E. Coli Product in Allergy Diagnosis.

Authors:  Öykü Üzülmez; Tanja Kalic; Vanessa Mayr; Nina Lengger; Angelika Tscheppe; Christian Radauer; Christine Hafner; Wolfgang Hemmer; Heimo Breiteneder
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4.  Insights into the SAM Synthetase Gene Family and Its Roles in Tomato Seedlings under Abiotic Stresses and Hormone Treatments.

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  4 in total

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