Literature DB >> 21822901

Refolding of proteins from inclusion bodies: rational design and recipes.

Anindya Basu1, Xiang Li, Susanna Su Jan Leong.   

Abstract

The need to develop protein biomanufacturing platforms that can deliver proteins quickly and cost-effectively is ever more pressing. The rapid rate at which genomes can now be sequenced demands efficient protein production platforms for gene function identification. There is a continued need for the biotech industry to deliver new and more effective protein-based drugs to address new diseases. Bacterial production platforms have the advantage of high expression yields, but insoluble expression of many proteins necessitates the development of diverse and optimised refolding-based processes. Strategies employed to eliminate insoluble expression are reviewed, where it is concluded that inclusion bodies are difficult to eliminate for various reasons. Rational design of refolding systems and recipes are therefore needed to expedite production of recombinant proteins. This review article discusses efforts towards rational design of refolding systems and recipes, which can be guided by the development of refolding screening platforms that yield both qualitative and quantitative information on the progression of a given refolding process. The new opportunities presented by light scattering technologies for developing rational protein refolding buffer systems which in turn can be used to develop new process designs armed with better monitoring and controlling functionalities are discussed. The coupling of dynamic and static light scattering methodologies for incorporation into future bioprocess designs to ensure delivery of high-quality refolded proteins at faster rates is also discussed.

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Year:  2011        PMID: 21822901     DOI: 10.1007/s00253-011-3513-y

Source DB:  PubMed          Journal:  Appl Microbiol Biotechnol        ISSN: 0175-7598            Impact factor:   4.813


  15 in total

1.  Soluble expression of pullulanase from Bacillus acidopullulyticus in Escherichia coli by tightly controlling basal expression.

Authors:  Ana Chen; Yamei Li; Xiuxia Liu; Quan Long; Yankun Yang; Zhonghu Bai
Journal:  J Ind Microbiol Biotechnol       Date:  2014-10-14       Impact factor: 3.346

2.  Dynamic transcriptional response of Escherichia coli to inclusion body formation.

Authors:  Faraz Baig; Lawrence P Fernando; Mary Alice Salazar; Rhonda R Powell; Terri F Bruce; Sarah W Harcum
Journal:  Biotechnol Bioeng       Date:  2014-01-30       Impact factor: 4.530

Review 3.  Design of Experiments As a Tool for Optimization in Recombinant Protein Biotechnology: From Constructs to Crystals.

Authors:  Christos Papaneophytou
Journal:  Mol Biotechnol       Date:  2019-12       Impact factor: 2.695

4.  Characterization of Polyamidoamino (PAMAM) Dendrimers Using In-Line Reversed Phase LC Electrospray Ionization Mass Spectrometry.

Authors:  John R Lloyd; P Suresh Jayasekara; Kenneth A Jacobson
Journal:  Anal Methods       Date:  2015-12-07       Impact factor: 2.896

5.  An automatic refolding apparatus for preparative-scale protein production.

Authors:  Yanye Feng; Ming Zhang; Linlin Zhang; Ting Zhang; Jianfeng Ding; Yingping Zhuang; Xiaoning Wang; Zhong Yang
Journal:  PLoS One       Date:  2012-09-27       Impact factor: 3.240

Review 6.  Recombinant protein expression in Escherichia coli: advances and challenges.

Authors:  Germán L Rosano; Eduardo A Ceccarelli
Journal:  Front Microbiol       Date:  2014-04-17       Impact factor: 5.640

7.  The aggregation of cytochrome C may be linked to its flexibility during refolding.

Authors:  James I Austerberry; Daniel J Belton
Journal:  3 Biotech       Date:  2016-01-14       Impact factor: 2.406

Review 8.  Protein fusion tags for efficient expression and purification of recombinant proteins in the periplasmic space of E. coli.

Authors:  Ajamaluddin Malik
Journal:  3 Biotech       Date:  2016-02-04       Impact factor: 2.406

9.  Expression of a fungal manganese peroxidase in Escherichia coli: a comparison between the soluble and refolded enzymes.

Authors:  Nan Wang; Kai Ren; Rong Jia; Wenting Chen; Ruirui Sun
Journal:  BMC Biotechnol       Date:  2016-12-01       Impact factor: 2.563

Review 10.  Inclusion bodies: not that bad….

Authors:  Ana Ramón; Mario Señorale-Pose; Mónica Marín
Journal:  Front Microbiol       Date:  2014-02-14       Impact factor: 5.640

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