Literature DB >> 31756040

A Simple Assay to Evaluate the Function of Human Connexin Hemichannels Expressed in Escherichia coli that Can Be Used for Drug Discovery and Mutant Analysis.

Mariana C Fiori1, Luis G Cuello1, Guillermo A Altenberg1.   

Abstract

Abnormally increased activity of connexin hemichannels contributes to cell damage in many disorders, including deafness, stroke, and cardiac infarct, and therefore hemichannels constitute a potentially important therapeutic target. Unfortunately, the available hemichannel inhibitors are not specific and most are toxic. The absence of a simple and cost-effective screening assay has made the discovery of hemichannel inhibitors difficult. Here, we present an optimized assay where human connexins are expressed in genetically modified Escherichia coli cells deficient in potassium uptake (LB2003 cells). These cells cannot grow in low-potassium medium, and hemichannel function is assayed by the reversion of the no-growth phenotype. Since functional hemichannels are permeable to potassium, they allow for its uptake and cell growth. The simple reading of bacterial growth in low-potassium medium distinguishes functional hemichannels (growth) from those inhibited (no growth). This assay is simple, robust, inexpensive, and reliable, and is easily scaled to high-throughput multiwell platforms.
© 2019 by John Wiley & Sons, Inc. Basic Protocol 1: Preparation of competent LB2003 cells resistant to kanamycin Basic Protocol 2: Growth complementation assay Support Protocol: Evaluation of cytotoxic effects of potential connexin hemichannel inhibitors. © 2019 John Wiley & Sons, Inc.

Entities:  

Keywords:  aminoglycoside; cell-based assay; channel; permeability; transport

Mesh:

Substances:

Year:  2019        PMID: 31756040      PMCID: PMC6876698          DOI: 10.1002/cpph.68

Source DB:  PubMed          Journal:  Curr Protoc Pharmacol        ISSN: 1934-8282


  26 in total

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Authors: 
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Authors:  Zhuyin Li; Yongping Yan; Elaine A Powers; Xiaoyou Ying; Khurram Janjua; Tina Garyantes; Bruce Baron
Journal:  J Biomol Screen       Date:  2003-10

Review 3.  Evolutionary analyses of gap junction protein families.

Authors:  Federico Abascal; Rafael Zardoya
Journal:  Biochim Biophys Acta       Date:  2012-02-14

Review 4.  Connexin 43 is an emerging therapeutic target in ischemia/reperfusion injury, cardioprotection and neuroprotection.

Authors:  Rainer Schulz; Philipp Maximilian Görge; Anikó Görbe; Péter Ferdinandy; Paul D Lampe; Luc Leybaert
Journal:  Pharmacol Ther       Date:  2015-06-11       Impact factor: 12.310

5.  Inhibition of gap junction hemichannels by chloride channel blockers.

Authors:  S Eskandari; G A Zampighi; D W Leung; E M Wright; D D F Loo
Journal:  J Membr Biol       Date:  2002-02-05       Impact factor: 1.843

Review 6.  Connexin-26 mutations in deafness and skin disease.

Authors:  Jack R Lee; Thomas W White
Journal:  Expert Rev Mol Med       Date:  2009-11-19       Impact factor: 5.600

Review 7.  Do connexin 43 gap-junctional hemichannels activate and cause cell damage during ATP depletion of renal-tubule cells?

Authors:  L Vergara; X Bao; E Bello-Reuss; L Reuss
Journal:  Acta Physiol Scand       Date:  2003-09

8.  Hemichannels in cardiomyocytes open transiently during ischemia and contribute to reperfusion injury following brief ischemia.

Authors:  Kaori Shintani-Ishida; Koichi Uemura; Ken-ichi Yoshida
Journal:  Am J Physiol Heart Circ Physiol       Date:  2007-06-08       Impact factor: 4.733

9.  A high-throughput assay for connexin 43 (Cx43, GJA1) gap junctions using codon-optimized aequorin.

Authors:  Nazia Haq; David Grose; Emma Ward; Oiyee Chiu; Natalie Tigue; Simon J Dowell; Andrew J Powell; Mao Xiang Chen
Journal:  Assay Drug Dev Technol       Date:  2012-10-09       Impact factor: 2.471

10.  A new high-throughput screening-compatible gap junctional intercellular communication assay.

Authors:  Ju Yeon Lee; Eun Ju Choi; Jinu Lee
Journal:  BMC Biotechnol       Date:  2015-10-06       Impact factor: 2.563

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