Literature DB >> 24674074

Explanatory chapter: troubleshooting recombinant protein expression: general.

Krisna C Duong-Ly1, Sandra B Gabelli2.   

Abstract

One of the most daunting problems for biochemists is the expression of recombinant proteins. Often, the host organism differs from the organism from which the gene coding for the protein of interest was derived. This article provides guidelines to determine whether or not protein expression is a problem, describes possible reasons for low protein expression, and covers several possible solutions. A protocol for measuring protein expression during E. coli cell growth and after induction is given. The reader should note that low protein expression is a complex problem that often stems from a variety of factors. Combinations of the solutions presented in this article may be required to solve a problem of protein expression. A brief overview of host cell expression systems is given, but the article primarily focuses on expression in E. coli as this is the most commonly used host organism. Some of the methods discussed here, however, may be applied to other expression systems.
© 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  E. coli cell growth; Eukaryotic expression systems; Miniprep DNA; T7 RNA polymerase; T7 expression vectors; XL1-Blue cells

Mesh:

Substances:

Year:  2014        PMID: 24674074     DOI: 10.1016/B978-0-12-420119-4.00017-3

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  4 in total

1.  A FRET-based method for monitoring septin polymerization and binding of septin-associated proteins.

Authors:  E A Booth; J Thorner
Journal:  Methods Cell Biol       Date:  2016-06-14       Impact factor: 1.441

2.  Thermococcus kodakarensis provides a versatile hyperthermophilic archaeal platform for protein expression.

Authors:  Kristin A Scott; Sere A Williams; Thomas J Santangelo
Journal:  Methods Enzymol       Date:  2021-07-13       Impact factor: 1.600

3.  Kinetic and mutational studies of the adenosine diphosphate ribose hydrolase from Mycobacterium tuberculosis.

Authors:  Suzanne F O'Handley; Puchong Thirawatananond; Lin-Woo Kang; Jennifer E Cunningham; J Alfonso Leyva; L Mario Amzel; Sandra B Gabelli
Journal:  J Bioenerg Biomembr       Date:  2016-09-28       Impact factor: 2.945

4.  Microfluidic platform for efficient Nanodisc assembly, membrane protein incorporation, and purification.

Authors:  James H Wade; Joshua D Jones; Ivan L Lenov; Colleen M Riordan; Stephen G Sligar; Ryan C Bailey
Journal:  Lab Chip       Date:  2017-08-22       Impact factor: 6.799

  4 in total

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