Abstract
A monoclonal antibody directed against the BK virus large T-antigen (clone BK.T-1) has previously been used to evaluate BKV-T antigen (BKV-TAg) expression. However, our experience showed a consistent reactivity to uninfected human, but not rodent cells and tissues. Using immunoprecipitation, Western analysis, amino acid sequencing and end-point dilution analysis, we analysed the BK.T-1 antibody reactivity and identified the bound cellular protein. The results clearly show that the antibody recognizes the large subunit (Ku86) of the Ku autoantigen, the regulatory component of the DNA-PKcs. We also demonstrated that the antibody retained its original reactivity in BKV-TAg transformed hamster kidney cells. The cross-reaction of the BK.T-1 antibody suggests a possible similarity between BKV-TAg and Ku86, but makes the antibody unsuitable for studies of BKV large T-antigen in the human cells.
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Acknowledgements
We are grateful to S Hirst for her excellent technical assistance and to Dr A Simoneau from the Department of Urology, VA Hospital, Long Beach, California, USA, for providing the prostate specimens. The work was supported by California Cancer Research Program grant to L Villarreal.
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Zambrano, A., Villarreal, L. A monoclonal antibody specific for BK virus large T-antigen (clone BK.T-1) also binds the human Ku autoantigen. Oncogene 21, 5725–5732 (2002). https://doi.org/10.1038/sj.onc.1205692
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DOI: https://doi.org/10.1038/sj.onc.1205692


