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. 2017 Jan 5;7:2129. doi: 10.3389/fmicb.2016.02129

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Copyright © 2017 Huang, Chen, Wang, Hsu, Tsai, Liu and Chang.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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MALDI-TOF mass spectrometry analysis of proteins that interact with Rta. (A) P3HR1 cells were treated with TPA and sodium butyrate for 24 h to induce the EBV lytic cycle and Rta expression. Cells were then lysed, and proteins in the lysate were immunoprecipitated (IP) with anti-Rta or anti-IgG antibodies. Immunoprecipitated proteins were denatured and analyzed by 2-D polyacrylamide gel electrophoresis. (B) Proteins in prospective spots were digested with trypsin and analyzed by MALDI-TOF mass spectrometry. Proteins with peptide fingerprints matching those in the MSDB database are listed in the table at right. (C) Peptide sequences in TRIM5α matching those in the D21 proteins are underlined.