Related Experiment Video
Updated: Feb 3, 2026

Purification and Refolding to Amyloid Fibrils of His6-tagged Recombinant Shadoo Protein Expressed as Inclusion Bodies in E. coli
Published on: December 19, 2015
Test bacterial inclusion body for activity prior to start denaturing and refolding processes to obtain active
Seyedeh Roghayeh Hamidi1, Yaghoub Safdari2, Mehdi Sheikh Arabi2
1Department of Medical Biotechnology, Faculty of Advanced Technologies in Medicine, Golestan University of Medical Sciences, Gorgan, Iran.
Abstract:
One of a major drawbacks correlated with expressing antibody fragments in bacterial cells is insolubility, which is often regarded as an obstacle in obtaining active molecules. Recombinant proteins aggregated as inclusion bodies within bacterial cells are thought to be unfolded or misfolded, and therefore inactive. So, denaturing and refolding strategies, which are laborious and sometime inefficient, are used to obtain correctly-folded active proteins. In the current study, we show that large quantities of correctly folded and completely active scFv molecules are there in bacterial inclusion bodies; they only need to be isolated from inclusion bodies.
Related Concept Videos
Eukaryotic Transcription Activators
The binding domains are capable of recognizing and interacting with regulatory sequences on the DNA. These...
Protein Denaturation
Co-activators and Co-repressors
Activation Energy
Activation and Inactivation of G Proteins
Eukaryotic RNA Polymerases
All three eukaryotic RNAPs require specific transcription factors, of which the...

