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Evaluation of scFv protein recovery from E. coli by in vitro refolding and mild solubilization process.
Sarker, Animesh; Rathore, Abhishek Singh; Gupta, Rinkoo Devi.
Afiliación
  • Sarker A; Faculty of Life Sciences and Biotechnology, South Asian University, New Delhi, India.
  • Rathore AS; Faculty of Life Sciences and Biotechnology, South Asian University, New Delhi, India.
  • Gupta RD; Faculty of Life Sciences and Biotechnology, South Asian University, New Delhi, India. rdgupta@sau.ac.in.
Microb Cell Fact ; 18(1): 5, 2019 Jan 14.
Article en En | MEDLINE | ID: mdl-30642336
ABSTRACT

BACKGROUND:

The production of therapeutically active single chain variable fragment (scFv) antibody is still challenging in E. coli due to the aggregation propensity of recombinant protein into inclusion bodies (IBs). However, recent advancement of biotechnology has shown substantial recovery of bioactive protein from such insoluble IBs by solubilization and refolding processes. In addition, gene fusion technology has also widely been used to improve the soluble protein production using E. coli. This study demonstrates that mild-solubilization and in vitro refolding strategies, both are capable to recover soluble scFv protein from bacterial IBs, although the degree of success is greatly influenced by different fusion tags with the target protein.

RESULTS:

It was observed that the most commonly used fusion tag, i.e., maltose binding protein (MBP) was not only influenced the cytoplasmic expression in E. coli but also greatly improved the in vitro refolding yield of scFv protein. On the other hand, mild solubilization process potentially could recover soluble and functional scFv protein from non-classical IBs without assistance of any fusion tag and in vitro refolding step. The recovery yield achieved by mild solubilization process was also found higher than denaturation-refolding method except while scFv was refolded in fusion with MBP tag. Concomitantly, it was also observed that the soluble protein achieved by mild solubilization process was better structured and functionally more active than the one achieved by in vitro refolding method in the absence of MBP tag or refolding enhancer.

CONCLUSIONS:

Maltose binding protein tagged scFv has shown better refolding and solubility yields as compare to mild solubilization process. However, in terms of cost, time and tag free nature, mild solubilization method for scFv recovery from bacterial IBs is considerable for therapeutic application and further structural studies.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Escherichia coli / Anticuerpos de Cadena Única Idioma: En Revista: Microb Cell Fact Asunto de la revista: BIOTECNOLOGIA / MICROBIOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Escherichia coli / Anticuerpos de Cadena Única Idioma: En Revista: Microb Cell Fact Asunto de la revista: BIOTECNOLOGIA / MICROBIOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: India