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Article: Direct inactivation of viruses by MCP-1 and MCP-2, natural peptide antibiotics from rabbit leukocytes.

Lehrer, R I / Daher, K / Ganz, T / Selsted, M E

Journal of virology

1985  Volume 54, Issue 2, Page(s) 467–472

Abstract: ... We speculate that MCP-1 and MCP-2, peptides that are abundant in rabbit granulocytes and lung macrophages ... 1 or MCP-2 depended on peptide concentration and on the time, temperature, and pH of the incubation ... may contribute to antiviral defenses by mediating the direct inactivation of HSV-1 and selected other viruses. ...

Abstract Six homologous peptides were purified to homogeneity from rabbit granulocytes or alveolar macrophages and tested for their ability to inactivate herpes simplex virus type 1 (HSV-1). Two of the peptides, MCP-1 and MCP-2, showed considerable in vitro neutralizing activity, whereas four structurally homologous peptides (NP-3a, NP-3b, NP-4, and NP-5) were relatively ineffective. Inactivation of HSV-1 by MCP-1 or MCP-2 depended on peptide concentration and on the time, temperature, and pH of the incubation. HSV-2, vesicular stomatitis virus, and influenza virus A/WSN were also susceptible to direct neutralization by MCP-1 or MCP-2, whereas cytomegalovirus, echovirus type 11, and reovirus type 3 were not. We speculate that MCP-1 and MCP-2, peptides that are abundant in rabbit granulocytes and lung macrophages, may contribute to antiviral defenses by mediating the direct inactivation of HSV-1 and selected other viruses.
MeSH term(s) Animals ; Anti-Infective Agents/pharmacology ; Antimicrobial Cationic Peptides ; Leukocytes/analysis ; Leukocytes/immunology ; Proteins/analysis ; Proteins/pharmacology ; Rabbits ; Simplexvirus/drug effects ; Structure-Activity Relationship ; Viruses/drug effects
Chemical Substances Anti-Infective Agents ; Antimicrobial Cationic Peptides ; Proteins
Language English
Publishing date 1985-05
Publishing country United States
Document type Journal Article ; Research Support, U.S. Gov't, P.H.S.
ZDB-ID 80174-4
ISSN 1098-5514 ; 0022-538X
ISSN (online) 1098-5514
ISSN 0022-538X
DOI 10.1128/JVI.54.2.467-472.1985
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