Literature DB >> 20821442

Phage display as a novel screening tool for primary toxicological targets.

Bieke Van Dorst1, Wim De Coen, Ronny Blust, Johan Robbens.   

Abstract

In the present study the use of phage display as a screening tool to determine primary toxicological targets was investigated. These primary toxicological targets are the targets in the cell with which a chemical compound initially interacts and that are responsible for consecutive (toxic) effects. Nickel was used as model compound for the present study. By selection of Ni-binding peptides out of a 12-mer peptide phage library, it was possible to identify primary toxicological targets of Ni (and other metals). The selected Ni-binding peptides showed similarities to important primary toxicological targets of Ni, such as the hydrogenase nickel incorporation protein (hypB) and the Mg/Ni/Co transporter (corA). This shows that phage display, which is already widely used in other research fields, also has potential in ecotoxicology, as a novel screening tool with which to determine primary toxicological targets of chemical compounds. Copyright 2009 SETAC.

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Year:  2010        PMID: 20821442     DOI: 10.1002/etc.38

Source DB:  PubMed          Journal:  Environ Toxicol Chem        ISSN: 0730-7268            Impact factor:   3.742


  2 in total

1.  Utilizing Yeast Surface Human Proteome Display Libraries to Identify Small Molecule-Protein Interactions.

Authors:  Scott Bidlingmaier; Bin Liu
Journal:  Methods Mol Biol       Date:  2015

2.  M13 phage peptide ZL4 exerts its targeted binding effect on schistosoma japonicum via alkaline phosphatase.

Authors:  Yan Liu; Shenghui Yang; Jianhua Xiao; Liang Yu; Li Chen; Ju Zou; Kegeng Wang; Sijie Tan; Zhengyang Yu; Qingren Zeng
Journal:  Int J Clin Exp Pathol       Date:  2015-02-01
  2 in total

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