Literature DB >> 2985803

A single amino acid substitution in a hydrophobic domain causes temperature-sensitive cell-surface transport of a mutant viral glycoprotein.

C J Gallione, J K Rose.   

Abstract

DNA sequences were determined for three cDNA clones encoding vesicular stomatitis virus glycoproteins from the tsO45 mutant (which encodes a glycoprotein that exhibits temperature-sensitive cell-surface transport), the wild-type parent strain, and a spontaneous revertant of tsO45. The DNA sequence analysis showed that as many as three amino acid changes could be responsible for the transport defect. By recombining the cDNA clones in vitro and expressing the recombinants in COS cells, we were able to trace the critical lesion in tsO45 to a single substitution of a polar amino acid (serine) for a hydrophobic amino acid (phenylalanine) in a hydrophobic domain. We suggest that this nonconservative substitution may block protein transport by causing protein denaturation at the nonpermissive temperature. Comparison of the predicted glycoprotein sequences from two vesicular stomatitis virus strains suggests a possible basis for the differential carbohydrate requirement in transport of the two glycoproteins.

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Year:  1985        PMID: 2985803      PMCID: PMC254807     

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  32 in total

1.  Maturation of viral proteins in cells infected with temperature-sensitive mutants of vesicular stomatitis virus.

Authors:  D M Knipe; D Baltimore; H F Lodish
Journal:  J Virol       Date:  1977-03       Impact factor: 5.103

2.  Synthesis and infectivity of vesicular stomatitis virus containing nonglycosylated G protein.

Authors:  R Gibson; R Leavitt; S Kornfeld; S Schlesinger
Journal:  Cell       Date:  1978-04       Impact factor: 41.582

3.  Impaired intracellular migration and altered solubility of nonglycosylated glycoproteins of vesicular stomatitis virus and Sindbis virus.

Authors:  R Leavitt; S Schlesinger; S Kornfeld
Journal:  J Biol Chem       Date:  1977-12-25       Impact factor: 5.157

4.  Synchronised transmembrane insertion and glycosylation of a nascent membrane protein.

Authors:  J E Rothman; H F Lodish
Journal:  Nature       Date:  1977-10-27       Impact factor: 49.962

5.  A new method for sequencing DNA.

Authors:  A M Maxam; W Gilbert
Journal:  Proc Natl Acad Sci U S A       Date:  1977-02       Impact factor: 11.205

6.  Envelope proteins of vesicular stomatitis virus: effect of temperature-sensitive mutations in complementation groups III and V.

Authors:  F Lafay
Journal:  J Virol       Date:  1974-11       Impact factor: 5.103

7.  [Genetic study of vesicular stomatitis virus: classification of spontaneous thermosensitive mutants into complementation groups].

Authors:  A Flamand
Journal:  J Gen Virol       Date:  1970-09       Impact factor: 3.891

8.  Surface structure of vesicular stomatitis virus.

Authors:  B Cartwright; C J Smale; F Brown
Journal:  J Gen Virol       Date:  1969-07       Impact factor: 3.891

9.  Cleavage of structural proteins during the assembly of the head of bacteriophage T4.

Authors:  U K Laemmli
Journal:  Nature       Date:  1970-08-15       Impact factor: 49.962

10.  Purification and properties of an endo-beta-N-acetylglucosaminidase from Streptomyces griseus.

Authors:  A L Tarentino; F Maley
Journal:  J Biol Chem       Date:  1974-02-10       Impact factor: 5.157

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  72 in total

1.  Assembly of the coronavirus envelope: homotypic interactions between the M proteins.

Authors:  C A de Haan; H Vennema; P J Rottier
Journal:  J Virol       Date:  2000-06       Impact factor: 5.103

2.  Osmotically induced cell volume changes alter anterograde and retrograde transport, Golgi structure, and COPI dissociation.

Authors:  T H Lee; A D Linstedt
Journal:  Mol Biol Cell       Date:  1999-05       Impact factor: 4.138

3.  A Rab2 mutant with impaired GTPase activity stimulates vesicle formation from pre-Golgi intermediates.

Authors:  E J Tisdale
Journal:  Mol Biol Cell       Date:  1999-06       Impact factor: 4.138

4.  Potential role for protein kinases in regulation of bidirectional endoplasmic reticulum-to-Golgi transport revealed by protein kinase inhibitor H89.

Authors:  T H Lee; A D Linstedt
Journal:  Mol Biol Cell       Date:  2000-08       Impact factor: 4.138

5.  Quantitative ER <--> Golgi transport kinetics and protein separation upon Golgi exit revealed by vesicular integral membrane protein 36 dynamics in live cells.

Authors:  T Dahm; J White; S Grill; J Füllekrug; E H Stelzer
Journal:  Mol Biol Cell       Date:  2001-05       Impact factor: 4.138

6.  Activation of mammalian unfolded protein response is compatible with the quality control system operating in the endoplasmic reticulum.

Authors:  Satomi Nadanaka; Hiderou Yoshida; Fumi Kano; Masayuki Murata; Kazutoshi Mori
Journal:  Mol Biol Cell       Date:  2004-03-12       Impact factor: 4.138

7.  ERdj3, a stress-inducible endoplasmic reticulum DnaJ homologue, serves as a cofactor for BiP's interactions with unfolded substrates.

Authors:  Ying Shen; Linda M Hendershot
Journal:  Mol Biol Cell       Date:  2004-11-03       Impact factor: 4.138

8.  Simulations of (an)isotropic diffusion on curved biological surfaces.

Authors:  Ivo F Sbalzarini; Arnold Hayer; Ari Helenius; Petros Koumoutsakos
Journal:  Biophys J       Date:  2005-11-11       Impact factor: 4.033

9.  GRASP65 and GRASP55 sequentially promote the transport of C-terminal valine-bearing cargos to and through the Golgi complex.

Authors:  Giovanni D'Angelo; Libera Prencipe; Luisa Iodice; Galina Beznoussenko; Marco Savarese; Pierfrancesco Marra; Giuseppe Di Tullio; Gianluca Martire; Maria Antonietta De Matteis; Stefano Bonatti
Journal:  J Biol Chem       Date:  2009-10-19       Impact factor: 5.157

10.  Role of heterologous and homologous glycoproteins in phenotypic mixing between Sendai virus and vesicular stomatitis virus.

Authors:  K Metsikkö; H Garoff
Journal:  J Virol       Date:  1989-12       Impact factor: 5.103

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