Literature DB >> 3656418

Organization of the Sindbis virus nucleocapsid as revealed by bifunctional cross-linking agents.

K Coombs1, D T Brown.   

Abstract

Purified Sindbis virus nucleocapsids were reacted with a variety of bifunctional protein-specific cross-linking agents. The products were analyzed in concentration-gradient polyacrylamide gels and amounts of various products determined. These studies indicated that available lysine residues within adjacent capsid proteins in purified intact nucleocapsids are separated by 6 A. The capsid proteins in intact nucleocapsids are cross-linked in a pattern predicted for discrete monomeric entities, rather than in dimeric or trimeric aggregates. Purified, soluble capsid protein exists in a conformation that differs from the arrangement of protein within nucleocapsids. These conformational differences suggest that topological changes may occur in the capsid protein during virus maturation. Cross-linked nucleocapsids that were treated with RNases resulted in the generation of RNA-free protein shells that retained hexagonal morphology, indicating that, together, the RNA and protein form the outer surface of the nucleocapsid. These data are used to produce a model of the Sindbis virus nucleocapsid in which the proteins are arranged quasi-equivalently in a T = 4 icosahedral shell.

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Year:  1987        PMID: 3656418     DOI: 10.1016/0022-2836(87)90657-7

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  23 in total

1.  A single deletion in the membrane-proximal region of the Sindbis virus glycoprotein E2 endodomain blocks virus assembly.

Authors:  R Hernandez; H Lee; C Nelson; D T Brown
Journal:  J Virol       Date:  2000-05       Impact factor: 5.103

2.  In vitro assembly of Sindbis virus core-like particles from cross-linked dimers of truncated and mutant capsid proteins.

Authors:  T L Tellinghuisen; R Perera; R J Kuhn
Journal:  J Virol       Date:  2001-03       Impact factor: 5.103

3.  A heterologous coiled coil can substitute for helix I of the Sindbis virus capsid protein.

Authors:  Rushika Perera; Chanakha Navaratnarajah; Richard J Kuhn
Journal:  J Virol       Date:  2003-08       Impact factor: 5.103

4.  Proteolytic processing of the Sindbis virus membrane protein precursor PE2 is nonessential for growth in vertebrate cells but is required for efficient growth in invertebrate cells.

Authors:  J F Presley; J M Polo; R E Johnston; D T Brown
Journal:  J Virol       Date:  1991-04       Impact factor: 5.103

5.  Protein-protein interactions in an alphavirus membrane.

Authors:  R P Anthony; D T Brown
Journal:  J Virol       Date:  1991-03       Impact factor: 5.103

6.  Structural localization of the E3 glycoprotein in attenuated Sindbis virus mutants.

Authors:  A M Paredes; H Heidner; P Thuman-Commike; B V Prasad; R E Johnston; W Chiu
Journal:  J Virol       Date:  1998-02       Impact factor: 5.103

7.  The formation of intramolecular disulfide bridges is required for induction of the Sindbis virus mutant ts23 phenotype.

Authors:  M Carleton; D T Brown
Journal:  J Virol       Date:  1997-10       Impact factor: 5.103

8.  Form-determining functions in Sindbis virus nucleocapsids: nucleosomelike organization of the nucleocapsid.

Authors:  K M Coombs; D T Brown
Journal:  J Virol       Date:  1989-02       Impact factor: 5.103

9.  Synthetic "interface" peptides alter dimeric assembly of the HIV 1 and 2 proteases.

Authors:  L M Babé; J Rosé; C S Craik
Journal:  Protein Sci       Date:  1992-10       Impact factor: 6.725

10.  Sindbis virus membrane fusion is mediated by reduction of glycoprotein disulfide bridges at the cell surface.

Authors:  B A Abell; D T Brown
Journal:  J Virol       Date:  1993-09       Impact factor: 5.103

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