Literature DB >> 3053710

Characterization of dolichol diphosphate oligosaccharide: protein oligosaccharyltransferase and glycoprotein-processing glucosidases occurring in trypanosomatid protozoa.

M Bosch1, S Trombetta, U Engstrom, A J Parodi.   

Abstract

We have previously reported that the oligosaccharides transferred in vivo from dolichol-P-P derivatives in protein N-glycosylation in trypanosomatids are devoid of glucose residues and contain 2 N-acetylglucosamine and 6, 7, or 9 mannose units depending on the species. In this respect trypanosomatids differ from wild type mammalian, plant, insect, and fungal cells in which Glc3Man9GlcNAc2 is transferred. We are now reporting that incubation of Glc1-3Man9GlcNAc2-P-P-dolichol and Man7-9GlcNAc2-P-P-dolichol with membranes of Trypanosoma cruzi, Leptomonas samueli, Crithidia fasciculata, and Blastocrithidia culicis and an acceptor hexapeptide leads to the transfer of the six above mentioned lipid-linked oligosaccharides at the same rate. Control experiments performed under similar conditions but with rat liver and Saccharomyces cerevisiae membranes showed that, as already known, Glc3Man9GlcNAc2 is preferentially transferred in the latter systems. We have also previously reported that, once transferred to protein, the oligosaccharides become transiently glucosylated in trypanosomatids. Depending on the species, protein-linked Glc1Man5-9GlcNAc2 have been transiently detected in cells incubated with [14C] glucose. We are now reporting that glucosidase activities degrading both Glc1Man9GlcNAc2 and Glc2Man9GlcNAc2 were detected in T. cruzi, L. samueli, and C. fasciculata. The enzymatic activities were associated with a membrane fraction; they had a neutral optimum pH value, and similarly to mammalian glucosidase II, the enzyme acting on the monoglucosylated substrate showed a decreased affinity when the latter contained fewer mannose residues. No glucosidase I-like enzyme acting on Glc3Man9GlcNAc2 was detected in any of the three above-mentioned protozoan species. This result is consistent with the fact that no oligosaccharides containing 3 glucose units occur in trypanosomatids.

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Year:  1988        PMID: 3053710

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  15 in total

Review 1.  N-glycoprotein macroheterogeneity: biological implications and proteomic characterization.

Authors:  Lucia F Zacchi; Benjamin L Schulz
Journal:  Glycoconj J       Date:  2015-12-05       Impact factor: 2.916

Review 2.  Role of N-oligosaccharide endoplasmic reticulum processing reactions in glycoprotein folding and degradation.

Authors:  A J Parodi
Journal:  Biochem J       Date:  2000-05-15       Impact factor: 3.857

3.  Trypanosoma cruzi calreticulin is a lectin that binds monoglucosylated oligosaccharides but not protein moieties of glycoproteins.

Authors:  C Labriola; J J Cazzulo; A J Parodi
Journal:  Mol Biol Cell       Date:  1999-05       Impact factor: 4.138

4.  Functional cooperation between BiP and calreticulin in the folding maturation of a glycoprotein in Trypanosoma cruzi.

Authors:  Carlos A Labriola; Ana M Villamil Giraldo; Armando J Parodi; Julio J Caramelo
Journal:  Mol Biochem Parasitol       Date:  2010-10-08       Impact factor: 1.759

5.  Preferential transfer of the complete glycan is determined by the oligosaccharyltransferase complex and not by the catalytic subunit.

Authors:  Olga Castro; Federico Movsichoff; Armando J Parodi
Journal:  Proc Natl Acad Sci U S A       Date:  2006-09-25       Impact factor: 11.205

Review 6.  Effects of N-glycan precursor length diversity on quality control of protein folding and on protein glycosylation.

Authors:  John Samuelson; Phillips W Robbins
Journal:  Semin Cell Dev Biol       Date:  2014-12-02       Impact factor: 7.727

7.  The interplay between folding-facilitating mechanisms in Trypanosoma cruzi endoplasmic reticulum.

Authors:  Ianina Conte; Carlos Labriola; Juan J Cazzulo; Roberto Docampo; Armando J Parodi
Journal:  Mol Biol Cell       Date:  2003-06-27       Impact factor: 4.138

8.  A misfolded protein conformation is not a sufficient condition for in vivo glucosylation by the UDP-Glc:glycoprotein glucosyltransferase.

Authors:  F Fernández; C D'Alessio; S Fanchiotti; A J Parodi
Journal:  EMBO J       Date:  1998-10-15       Impact factor: 11.598

9.  All in one: Leishmania major STT3 proteins substitute for the whole oligosaccharyltransferase complex in Saccharomyces cerevisiae.

Authors:  Farnoush Parsaie Nasab; Benjamin L Schulz; Francisco Gamarro; Armando J Parodi; Markus Aebi
Journal:  Mol Biol Cell       Date:  2008-07-02       Impact factor: 4.138

Review 10.  Glycosylation in parasitic protozoa of the trypanosomatidae family.

Authors:  S Zamze
Journal:  Glycoconj J       Date:  1991-12       Impact factor: 2.916

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