Literature DB >> 7873528

Purification and properties of a Golgi-derived (alpha 1,2)-mannosidase-I from baculovirus-infected lepidopteran insect cells (IPLB-SF21AE) with preferential activity toward mannose6-N-acetylglucosamine2.

J Ren1, R K Bretthauer, F J Castellino.   

Abstract

Because the availability and subcellular distribution of processing mannosidases in cells play such powerful roles in determining ultimate structures of glycoconjugates, we desired to identify, characterize, and investigate possible regulation of mannosidases in infected and noninfected lepidopteran insect cells. Since our previous observations that a mannosidase activity that converted Man6GlcNAc2 to Man5GlcNAc2 was enhanced in virus-infected cells, thus providing the necessary intermediate for further processing to complex-type oligosaccharides, we attempted purification of this enzyme. A mannosidase was isolated and purified from membranes, operationally defined as Golgi, of recombinant baculovirus-infected Spodoptera frugiperda (IPLB-SF-21AE) cells. The molecular mass of this protein was approximately 63 kDa. Assays performed by measuring the conversion of NaB3H4-reduced Man6GlcNAc2-ol to Man5GlcNAc-[3H]GlcNAc2-ol demonstrated that the mannosidase activity was dependent on the presence of divalent cations, which was optimal for Ca2+ at pH 6.0. Inclusion of 1-deoxymannojirimycin resulted in 50% inhibition at a concentration of 20 microM, whereas swainsonine did not show such inhibition. No activity was observed with p-nitrophenyl alpha-D-mannoside (4 mM) as a substrate. The preferred reduced oligosaccharide substrate was Man6GlcNAc2-ol, with lower activities obtained with Man9GlcNAc2-ol, Man8GlcNAc2-ol, and Man7GlcNAc2-ol. With Man6GlcNAc2-ol as substrate, products smaller than reduced Man5GlcNAc2-ol were not observed. Mannose was also liberated from the glycoprotein, ovalbumin. These properties are consistent with an enzyme classification as a type I (alpha 1,2)-Man6-mannosidase.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7873528     DOI: 10.1021/bi00008a012

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  6 in total

1.  Expression and functional characterization of a nucleotide sugar transporter from Drosophila melanogaster: relevance to protein glycosylation in insect cell expression systems.

Authors:  Jared J Aumiller; Donald L Jarvis
Journal:  Protein Expr Purif       Date:  2002-12       Impact factor: 1.650

2.  Purification and properties of alpha-mannosidase II from Golgi-like membranes of baculovirus-infected Spodoptera frugiperda (IPLB-SF-21AE) cells.

Authors:  J Ren; F J Castellino; R K Bretthauer
Journal:  Biochem J       Date:  1997-06-15       Impact factor: 3.857

3.  Structural characterization of the N-linked oligosaccharides derived from HIVgp120 expressed in lepidopteran cells.

Authors:  T D Butters; B Yudkin; G S Jacob; I M Jones
Journal:  Glycoconj J       Date:  1998-01       Impact factor: 2.916

Review 4.  Comparing N-glycan processing in mammalian cell lines to native and engineered lepidopteran insect cell lines.

Authors:  Noboru Tomiya; Someet Narang; Yuan C Lee; Michael J Betenbaugh
Journal:  Glycoconj J       Date:  2004       Impact factor: 2.916

5.  Molecular cloning and functional characterization of a Lepidopteran insect beta4-N-acetylgalactosaminyltransferase with broad substrate specificity, a functional role in glycoprotein biosynthesis, and a potential functional role in glycolipid biosynthesis.

Authors:  Nadia Vadaie; Donald L Jarvis
Journal:  J Biol Chem       Date:  2004-06-01       Impact factor: 5.157

6.  The ALK inhibitor PF-06463922 is effective as a single agent in neuroblastoma driven by expression of ALK and MYCN.

Authors:  J Guan; E R Tucker; H Wan; D Chand; L S Danielson; K Ruuth; A El Wakil; B Witek; Y Jamin; G Umapathy; S P Robinson; T W Johnson; T Smeal; T Martinsson; L Chesler; R H Palmer; B Hallberg
Journal:  Dis Model Mech       Date:  2016-07-07       Impact factor: 5.758

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.