Analytical characterization of in vitro refolding in the quality by design paradigm: Refolding of recombinant human granulocyte colony stimulating factor
Autor: | S. Muthukumar, Shruti Dixit, Mili Pathak, Anurag S. Rathore |
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Rok vydání: | 2016 |
Předmět: |
0301 basic medicine
Clinical Biochemistry Pharmaceutical Science Nanotechnology Computational biology 01 natural sciences Protein Refolding Inclusion bodies Quality by Design Analytical Chemistry law.invention 03 medical and health sciences law Granulocyte Colony-Stimulating Factor Drug Discovery Escherichia coli Humans Technology Pharmaceutical Spectroscopy Inclusion Bodies Chemistry 010401 analytical chemistry Model protein Therapeutic protein Recombinant Proteins In vitro 0104 chemical sciences Granulocyte colony-stimulating factor 030104 developmental biology Protein refolding Recombinant DNA |
Zdroj: | Journal of Pharmaceutical and Biomedical Analysis. 126:124-131 |
ISSN: | 0731-7085 |
DOI: | 10.1016/j.jpba.2016.05.001 |
Popis: | Protein based therapeutics dominate most pharmaceutical pipelines today. For a therapeutic product to be effective, it is important that it is in its native form as slight modifications have been known to result in significantly different performance in the clinic. When expressed in hosts such as Escherichia coli, formation of inactive insoluble aggregates of proteins popularly known as inclusion bodies occurs in most cases. This necessitates the need for in vitro refolding to generate the native (and active) form of the therapeutic protein. This paper aims to provide an approach to generate a deeper understanding of refolding of a therapeutic protein and then to use it for its optimal production commercially. Recombinant human granulocyte colony stimulating factor has been chosen as the model protein. Seven orthogonal analytical tools have been used to elucidate the refolding process. By strategically using these tools protein refolding has been segregated into a series of well-defined sequence of events, starting from the unfolded random coil and ending with the uniquely folded metastable state. The study also suggests the choice of tools that can be used to monitor each event. We believe that this paper successfully demonstrates an approach to generate deeper understanding of the protein refolding process as per the expectations laid out in the Quality by Design paradigm. |
Databáze: | OpenAIRE |
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