An Escherichia coli strain for expression of the connexin45 carboxyl terminus attached to the 4th transmembrane domain

Jennifer L. Kopanic, Mona Al-Mugotir, Sydney Zach, Srustidhar Das, Rosslyn Grosely, Paul L Sorgen

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

A major problem for structural characterization of membrane proteins, such as connexins, by nuclear magnetic resonance (NMR) occurs at the initial step of the process, the production of sufficient amounts of protein. This occurs because proteins must be expressed in minimal based media. Here, we describe an expression system for membrane proteins that significantly improves yield by addressing two common problems, cell toxicity caused by protein translation and codon bias between genomes. This work provides researchers with a cost-effective tool for NMR and other biophysical studies, to use when faced with little-to-no expression of eukaryotic membrane proteins in Escherichia coli expression systems.

Original languageEnglish (US)
Article numberArticle 106
JournalFrontiers in Pharmacology
Volume4 AUG
DOIs
StatePublished - Sep 11 2013

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Membrane Proteins
Escherichia coli
Magnetic Resonance Spectroscopy
Connexins
Protein Biosynthesis
Codon
Proteins
Research Personnel
Genome
Costs and Cost Analysis

Keywords

  • Connexins
  • Membrane protein expression
  • Minimal media
  • NMR
  • Rare codons

ASJC Scopus subject areas

  • Pharmacology
  • Pharmacology (medical)

Cite this

An Escherichia coli strain for expression of the connexin45 carboxyl terminus attached to the 4th transmembrane domain. / Kopanic, Jennifer L.; Al-Mugotir, Mona; Zach, Sydney; Das, Srustidhar; Grosely, Rosslyn; Sorgen, Paul L.

In: Frontiers in Pharmacology, Vol. 4 AUG, Article 106, 11.09.2013.

Research output: Contribution to journalArticle

Kopanic, Jennifer L. ; Al-Mugotir, Mona ; Zach, Sydney ; Das, Srustidhar ; Grosely, Rosslyn ; Sorgen, Paul L. / An Escherichia coli strain for expression of the connexin45 carboxyl terminus attached to the 4th transmembrane domain. In: Frontiers in Pharmacology. 2013 ; Vol. 4 AUG.
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