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Literature DB >> 7373709

Protein organization in Newcastle disease virus as revealed by perturbant treatment.

Abstract

Treatment of Newcastle disease virus with lithium diiodosalicylate differentially elutes the internally disposed proteins, M and NP, showing that these proteins are extrinsic, i.e., not associated with the lipid hydrophobic core. This selective elution requires disruption of the viral envelope, a process that is maximal at low temperature and influenced by the lipid composition of the virus envelope.

Entities: Chemical Species

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Year: 1980 PMID： 7373709 PMCID： PMC288693

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

22 in total

1. Effects of temperature and host lipid composition on the infection of cells by Newcastle disease virus.

Authors: J K Li; R E Williams; C F Fox
Journal: Biochem Biophys Res Commun Date: 1975-01-20 Impact factor: 3.575

2. The synthesis of Sendai virus polypeptides in infected cells. II. Intracellular distribution of polypeptides.

Authors: R A Lamb; P W Choppin
Journal: Virology Date: 1977-09 Impact factor: 3.616

3. Surface-specific iodination of membrane proteins of viruses and eucaryotic cells using 1,3,4,6-tetrachloro-3alpha,6alpha-diphenylglycoluril.

Authors: M A Markwell; C F Fox
Journal: Biochemistry Date: 1978-10-31 Impact factor: 3.162

4. Identification of biological activities of paramyxovirus glycoproteins. Activation of cell fusion, hemolysis, and infectivity of proteolytic cleavage of an inactive precursor protein of Sendai virus.

Authors: A Scheid; P W Choppin
Journal: Virology Date: 1974-02 Impact factor: 3.616

5. Selective solubilization of proteins and phospholipids from red blood cell membranes by nonionic detergents.

Authors: J Yu; D A Fischman; T L Steck
Journal: J Supramol Struct Date: 1973

6. Proteins and glycoproteins of paramyxoviruses: a comparison of simian virus 5, Newcastle disease virus, and Sendai virus.

Authors: W E Mountcastle; R W Compans; P W Choppin
Journal: J Virol Date: 1971-01 Impact factor: 5.103

Protein organization in Newcastle disease virus as revealed by perturbant treatment.

1. Effects of temperature and host lipid composition on the infection of cells by Newcastle disease virus.

2. The synthesis of Sendai virus polypeptides in infected cells. II. Intracellular distribution of polypeptides.

3. Surface-specific iodination of membrane proteins of viruses and eucaryotic cells using 1,3,4,6-tetrachloro-3alpha,6alpha-diphenylglycoluril.

4. Identification of biological activities of paramyxovirus glycoproteins. Activation of cell fusion, hemolysis, and infectivity of proteolytic cleavage of an inactive precursor protein of Sendai virus.

5. Selective solubilization of proteins and phospholipids from red blood cell membranes by nonionic detergents.

6. Proteins and glycoproteins of paramyxoviruses: a comparison of simian virus 5, Newcastle disease virus, and Sendai virus.

7. Proteins of four biologically distinct strains of Newcastle disease virus.

8. Homology of amino-terminal regions of C-phycocyanins from a prokaryote and a eukaryote.

9. Physical and physiological evidence for two phase transitions in cytoplasmic membranes of animal cells.

10. Nucleocapsid protein subunits of simian virus 5, Newcastle disease virus, and Sendai virus.

1. Nucleotide sequence of the gene encoding the matrix protein of Newcastle disease virus.

2. Ultrastructure and biochemistry of the cell wall of Methanococcus voltae.

3. Identification of the P proteins and other disulfide-linked and phosphorylated proteins of Newcastle disease virus.