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
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
Journal title :
Journal of Chromatography B