Literature DB >> 24211444

Production of prone-to-aggregate proteins.

Mario Lebendiker1, Tsafi Danieli2.   

Abstract

Expression of recombinant proteins in Escherichia coli (E. coli) remains the most popular and cost-effective method for producing proteins in basic research and for pharmaceutical applications. Despite accumulating experience and methodologies developed over the years, production of recombinant proteins prone to aggregate in E. coli-based systems poses a major challenge in most research applications. The challenge of manufacturing these proteins for pharmaceutical applications is even greater. This review will discuss effective methods to reduce and even prevent the formation of aggregates in the course of recombinant protein production. We will focus on important steps along the production path, which include cloning, expression, purification, concentration, and storage.
Copyright © 2013 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Aggregation analysis; Aggregation suppressor; Buffer condition; Chaotrope; Chaperone; Fusion protein; Induction condition; Intrinsically disordered protein; Intrinsically disordered region; Kosmotrope; Protein aggregation; Protein concentration; Protein storage; Stabilizer

Mesh:

Substances:

Year:  2013        PMID: 24211444     DOI: 10.1016/j.febslet.2013.10.044

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  42 in total

Review 1.  Stepwise optimization of recombinant protein production in Escherichia coli utilizing computational and experimental approaches.

Authors:  Kulandai Arockia Rajesh Packiam; Ramakrishnan Nagasundara Ramanan; Chien Wei Ooi; Lakshminarasimhan Krishnaswamy; Beng Ti Tey
Journal:  Appl Microbiol Biotechnol       Date:  2020-02-19       Impact factor: 4.813

2.  Assessing and Improving Protein Sample Quality.

Authors:  Bertrand Raynal; Sébastien Brûlé; Stephan Uebel; Stefan H Knauer
Journal:  Methods Mol Biol       Date:  2021

3.  Identification of FAM181A and FAM181B as new interactors with the TEAD transcription factors.

Authors:  Fedir Bokhovchuk; Yannick Mesrouze; Clara Delaunay; Typhaine Martin; Frédéric Villard; Marco Meyerhofer; Patrizia Fontana; Catherine Zimmermann; Dirk Erdmann; Pascal Furet; Clemens Scheufler; Tobias Schmelzle; Patrick Chène
Journal:  Protein Sci       Date:  2019-11-20       Impact factor: 6.725

Review 4.  New tools for recombinant protein production in Escherichia coli: A 5-year update.

Authors:  Germán L Rosano; Enrique S Morales; Eduardo A Ceccarelli
Journal:  Protein Sci       Date:  2019-07-01       Impact factor: 6.725

5.  Polyphosphates diminish solubility of a globular protein and thereby promote amyloid aggregation.

Authors:  Kenji Sasahara; Keiichi Yamaguchi; Masatomo So; Yuji Goto
Journal:  J Biol Chem       Date:  2019-08-22       Impact factor: 5.157

6.  Quarterly intrinsic disorder digest (January-February-March, 2014).

Authors:  Shelly DeForte; Krishna D Reddy; Vladimir N Uversky
Journal:  Intrinsically Disord Proteins       Date:  2016-02-12

Review 7.  Pioneer factors and their in vitro identification methods.

Authors:  Xinyang Yu; Michael J Buck
Journal:  Mol Genet Genomics       Date:  2020-04-15       Impact factor: 3.291

8.  Facile Synthesis and Characterization of a Novel Tamavidin-Luciferase Reporter Fusion Protein for Universal Signaling Applications.

Authors:  David B Broyles; Emre Dikici; Sylvia Daunert; Sapna K Deo
Journal:  Adv Biosyst       Date:  2020-02-28

Review 9.  Mechanistic and Structural Insights into the Prion-Disaggregase Activity of Hsp104.

Authors:  Elizabeth A Sweeny; James Shorter
Journal:  J Mol Biol       Date:  2015-12-01       Impact factor: 5.469

10.  Analysis of Methods to Improve the Solubility of Recombinant Bovine Sex Determining Region Y Protein.

Authors:  Bijan Soleymani; Ali Mostafaie
Journal:  Rep Biochem Mol Biol       Date:  2019-10
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