Arenavirus Z protein as an antiviral target: virus inactivation and protein oligomerization by zinc finger-reactive compounds

Several disulfide-based and azoic compounds have shown antiviral and virucidal properties against arenaviruses in virus yield-inhibition and inactivation assays, respectively. The most effective virucidal agent, the aromatic disulfide NSC20625, was able to inactivate two strains of the prototype are...

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Veröffentlicht in:Journal of general virology Jg. 87; H. Pt 5; S. 1217
Hauptverfasser: García, Cybele C, Djavani, Mahmoud, Topisirovic, Ivan, Borden, Katherine L B, Salvato, María S, Damonte, Elsa B
Format: Journal Article
Sprache:Englisch
Veröffentlicht: England 01.05.2006
Schlagworte:
Animals
Azo Compounds - chemistry
Azo Compounds - pharmacology
Carrier Proteins - drug effects
Cell Line
Disulfides - chemistry
Disulfides - pharmacology
Humans
Intracellular Signaling Peptides and Proteins
Lymphocytic choriomeningitis virus - drug effects
Lymphocytic choriomeningitis virus - physiology
Oligodeoxyribonucleotides - metabolism
RNA, Viral - biosynthesis
RNA, Viral - drug effects
Virus Replication - drug effects
Zinc Fingers - drug effects
ISSN:0022-1317
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Zusammenfassung:Several disulfide-based and azoic compounds have shown antiviral and virucidal properties against arenaviruses in virus yield-inhibition and inactivation assays, respectively. The most effective virucidal agent, the aromatic disulfide NSC20625, was able to inactivate two strains of the prototype arenavirus species Lymphocytic choriomeningitis virus (LCMV). Inactivated viral particles retained the biological functions of the virion envelope glycoproteins in virus binding and uptake, but were unable to perform viral RNA replication. Furthermore, in inactivated virions, the electrophoretic profile of the Z protein was altered when analysed under non-reducing conditions, whereas the patterns of the proteins NP and GP1 remained unaffected. Treatment of a recombinant LCMV Z protein with the virucidal agents induced unfolding and oligomerization of Z to high-molecular-mass aggregates, probably due to metal-ion ejection and the formation of intermolecular disulfide bonds through the cysteine residues of the Z RING finger. NSC20625 also exhibited antiviral properties in LCMV-infected cells without affecting other cellular RING-motif proteins, such as the promyelocytic leukaemia protein PML. Altogether, the investigations described here illustrate the potential of the Z protein as a promising target for therapy and the prospects of the Z-reactive compounds to prevent arenavirus dissemination.
Bibliographie:ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:0022-1317
DOI:10.1099/vir.0.81667-0