Literature DB >> 2321417

Mature, cell-associated HN protein of Newcastle disease virus exists in two forms differentiated by posttranslational modifications.

T G Morrison1, C McQuain, K F O'Connell, L W McGinnes.   

Abstract

Characterization of the posttranslational modifications of the mature, cell-associated hemagglutinin-neuraminidase (HN) protein of Newcastle disease virus (NDV) revealed that the HN protein exists in two forms differentiated by disulfide bonds and glycosylation. One form, HNa, contains intermolecular disulfide bonds and is endoglycosidase H partially resistant. The other form, HNb, is not linked by disulfide bonds and is endoglycosidase H sensitive. Both forms of the protein are modified with fucose indicating transport to the Golgi membranes. Both forms are detected at the cell surface by monoclonal antibody. Furthermore, both forms are transported to the cell surface with identical kinetics. HNa is incorporated into virions. HNb is not incorporated into virions and is presumably degraded. The cDNA derived from the HN gene was expressed from a retrovirus vector. The majority of the protein expressed was in the nonvirion-associated form b. Evidence is presented that the level of gene expression determines the ratio of the two forms of HN protein. At high levels of expression, the virion-associated form is favored while at low levels of expression the nonvirion-associated form is favored. The results presented have implications for persistent infections as well as expression of viral genes from different vectors.

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Year:  1990        PMID: 2321417     DOI: 10.1016/0168-1702(90)90003-t

Source DB:  PubMed          Journal:  Virus Res        ISSN: 0168-1702            Impact factor:   3.303


  9 in total

1.  Pathogenicity evaluation of different Newcastle disease virus chimeras in 4-week-old chickens.

Authors:  Leonardo Susta; Patti J Miller; Claudio L Afonso; Carlos Estevez; Qingzhong Yu; Jian Zhang; Corrie C Brown
Journal:  Trop Anim Health Prod       Date:  2010-07-08       Impact factor: 1.559

2.  Site-specific glycosylation of the Newcastle disease virus haemagglutinin-neuraminidase.

Authors:  Cassandra L Pegg; Christine Hoogland; Jeffrey J Gorman
Journal:  Glycoconj J       Date:  2016-12-07       Impact factor: 2.916

3.  Differences in the role of the cytoplasmic domain of human parainfluenza virus fusion proteins.

Authors:  Q Yao; R W Compans
Journal:  J Virol       Date:  1995-11       Impact factor: 5.103

4.  Mutations in the fusion peptide and heptad repeat regions of the Newcastle disease virus fusion protein block fusion.

Authors:  T Sergel-Germano; C McQuain; T Morrison
Journal:  J Virol       Date:  1994-11       Impact factor: 5.103

5.  Antiviral effect of N-butyldeoxynojirimycin against bovine viral diarrhea virus correlates with misfolding of E2 envelope proteins and impairment of their association into E1-E2 heterodimers.

Authors:  N Branza-Nichita; D Durantel; S Carrouée-Durantel; R A Dwek; N Zitzmann
Journal:  J Virol       Date:  2001-04       Impact factor: 5.103

6.  Disulfide bond formation is a determinant of glycosylation site usage in the hemagglutinin-neuraminidase glycoprotein of Newcastle disease virus.

Authors:  L W McGinnes; T G Morrison
Journal:  J Virol       Date:  1997-04       Impact factor: 5.103

7.  Detection of an interaction between the HN and F proteins in Newcastle disease virus-infected cells.

Authors:  J Stone-Hulslander; T G Morrison
Journal:  J Virol       Date:  1997-09       Impact factor: 5.103

8.  Mutational analysis of the leucine zipper motif in the Newcastle disease virus fusion protein.

Authors:  J N Reitter; T Sergel; T G Morrison
Journal:  J Virol       Date:  1995-10       Impact factor: 5.103

Review 9.  Paramyxovirus entry.

Authors:  Katharine N Bossart; Deborah L Fusco; Christopher C Broder
Journal:  Adv Exp Med Biol       Date:  2013       Impact factor: 2.622

  9 in total

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