• Title of article

    Purification of the proline-rich homeodomain protein

  • Author/Authors

    Butcher، نويسنده , , Amy J. and Gaston، نويسنده , , Kevin and Jayaraman، نويسنده , , Padma-Sheela Jayaraman، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2003
  • Pages
    4
  • From page
    3
  • To page
    6
  • Abstract
    The proline-rich homeodomain protein (PRH), also known as Hex, is a transcriptional repressor expressed in a variety of cell types. The PRH protein contains a proline-rich N-terminal domain that can repress transcription when attached to a heterologous DNA binding domain, a central homeodomain that mediates sequence-specific DNA binding, and an acidic C-terminal domain of unknown function. Although individual domains of PRH have been expressed in bacterial cells as GST- and histidine-tagged fusion proteins, attempts to express and purify the full-length protein have met with little success. Here we describe the purification of a histidine-tagged full-length PRH fusion protein. The protein described here will allow us to determine the mechanisms whereby PRH represses transcription.
  • Keywords
    Proline-rich homeodomain protein
  • Journal title
    Journal of Chromatography B
  • Serial Year
    2003
  • Journal title
    Journal of Chromatography B
  • Record number

    1454933