| Literature DB >> 12610165 |
Jayati Mullick1, John Bernet, Akhilesh K Singh, John D Lambris, Arvind Sahu.
Abstract
The genome analysis of Kaposi's sarcoma-associated herpesvirus (KSHV) has revealed the presence of an open reading frame (ORF 4) with sequence homology to complement control proteins. To assign a function to this protein, we have now expressed this ORF using the Pichia expression system and shown that the purified protein inhibited human complement-mediated lysis of erythrocytes, blocked cell surface deposition of C3b (the proteolytically activated form of C3), and served as a cofactor for factor I-mediated inactivation of complement proteins C3b and C4b (the subunits of C3 convertases). Thus, our data indicate that this KSHV inhibitor of complement activation (kaposica) provides a mechanism by which KSHV can subvert complement attack by the host.Entities:
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Year: 2003 PMID: 12610165 PMCID: PMC149522 DOI: 10.1128/jvi.77.6.3878-3881.2003
Source DB: PubMed Journal: J Virol ISSN: 0022-538X Impact factor: 5.103