1. Structural Analysis of the Kaposi's Sarcoma-Associated Herpesvirus K1 Protein
- Author
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Jae U. Jung, Bok-Soo Lee, Zuoquin Tang, Michelle Connole, and Nancy L. Harris
- Subjects
Lymphoma, B-Cell ,medicine.drug_class ,Immunoblotting ,Molecular Sequence Data ,Immunology ,Fluorescent Antibody Technique ,Enzyme-Linked Immunosorbent Assay ,Biology ,Antibodies, Viral ,Monoclonal antibody ,medicine.disease_cause ,Microbiology ,Epitope ,Mice ,Viral Proteins ,Virology ,Tumor Cells, Cultured ,medicine ,Extracellular ,Animals ,Humans ,Amino Acid Sequence ,Kaposi's sarcoma-associated herpesvirus ,Sarcoma, Kaposi ,Peptide sequence ,Mice, Inbred BALB C ,Castleman Disease ,Flow Cytometry ,Immunohistochemistry ,Molecular biology ,Virus-Cell Interactions ,Epitope mapping ,Insect Science ,Herpesvirus 8, Human ,Mutation ,biology.protein ,Calcium ,Lymph Nodes ,Signal transduction ,Antibody ,Epitope Mapping ,Signal Transduction - Abstract
The K1 protein of Kaposi's sarcoma-associated herpesvirus (KSHV) efficiently transduces extracellular signals to elicit cellular activation events through its cytoplasmic immunoreceptor tyrosine-based activation motif (ITAM). In addition, the extracellular domain of K1 demonstrates regional homology with the immunoglobulin (Ig) family and contains conserved regions (C1 and C2) and variable regions (V1 and V2). To generate mouse monoclonal antibodies directed against the KSHV K1 protein, BALB/c mice were primed and given boosters with K1 protein purified from mammalian cells. Twenty-eight hybridomas were tested for reactivity with K1 protein by enzyme-linked immunosorbent assay, immunofluorescence, flow cytometry, immunohistochemistry, and immunoblotting. Deletion mutants of the K1 extracellular domain were used to map the epitope of each antibody. All antibodies were directed to the Ig, C1, and C2 regions of K1. Furthermore, antibody recognition of a short sequence (amino acids 92 to 125) of the C2 region overlapping with the Ig region of K1 efficiently induced intracellular free calcium mobilization; antibody recognition of the other regions of K1 did not. The efficient signal transduction of K1 induced by antibody stimulation required both the ITAM sequence of the cytoplasmic domain and the normal structure of the extracellular domain. Finally, immunological assays showed that K1 was expressed during the early lytic cycle of viral replication in primary effusion lymphoma cells. K1 was readily detected in multicentric Castleman's disease tissues, whereas it was not detected in Kaposi's sarcoma lesions, suggesting that K1 is preferentially expressed in lymphoid cells. Thus, these results indicate that the conserved regions, particularly the Ig and C2 regions, of the K1 extracellular domain are exposed on the outer surface and play an important role in K1 structure and signal transduction, whereas the variable regions of K1 appear to be away from the surface.
- Published
- 2003
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