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Updated: Aug 13, 2026

Purification of Hsp104, a Protein Disaggregase
Published on: September 30, 2011
Refolding and one-step purification of recombinant human ARA70 over-expressed in Escherichia coli
Vinay Kumar Singh1, Zongchao Jia
1Department of Biochemistry, Queen's University, Kingston, Ont., Canada K7L 3N6.
Abstract:
Androgen receptor (AR)-associated coregulator 70 (ARA70) is a cytoplasmic protein that has been characterized to have the ability to induce AR transcriptional activity in response to androgens and anti-androgens in prostate cancer cells. AR has been shown to have an important role in the progression of prostate cancer and in normal male reproductive system development. To elucidate the molecular mechanisms and biological relevance of ARA70 to prostrate cancer using a variety of biochemical analyses, the cDNA encoding full length ARA70 was cloned into pET21b vector. Here, we report the refolding and one-step purification of ARA70 from inclusion bodies over-expressed in Escherichia coli. The protein was purified to homogeneity, yielding approximately 60 mg ARA70 from 1L of terrific broth media. Refolding process of ARA70 was monitored using far-UV CD analysis.

