4.8 Article

Cell-Free Protein Synthesis Approach to Biosensing hTR(ss)-Specific Endocrine Disruptors

Journal

ANALYTICAL CHEMISTRY
Volume 89, Issue 6, Pages 3395-3401

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.6b04034

Keywords

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Funding

  1. NIH grant [1R21ES16630]
  2. NSF CAREER Award [1254148]
  3. DARPA Young Faculty Award [D13AP000037]
  4. Div Of Chem, Bioeng, Env, & Transp Sys
  5. Directorate For Engineering [1254148] Funding Source: National Science Foundation

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Here we introduce a Rapid Adaptable Portable In vitro Detection biosensor platform (RAPID) for detecting ligands that interact with nuclear hormone receptors (NHRs). The RAPID platform can be adapted for field use, allowing rapid evaluation of endocrine disrupting chemicals (EDCs) presence or absence in environmental samples, and can also be applied for drug screening. The biosensor is based on an engineered, allosterically activated fusion protein, which contains the ligand binding domain from a target NHR (human thyroid receptor beta in this work). In vitro expression of this protein using cell-free protein synthesis (CEPS) technology in the presence of an EDC leads to activation of a reporter enzyme, reported through a straightforward colorimetric assay output. In this work, we demonstrate the potential of this biosensor platform to be used in a portable just-add-sample format for near real-time detection. We also demonstrate the robust nature of the cell-free protein synthesis component in the presence of a variety of environmental and human samples, including sewage, blood, and urine. The presented RAPID biosensor platform is significantly faster and less labor intensive then commonly available technologies,making it a promising tool for detecting environmental EDC contamination and screening potential NHR-targeted pharmaceuticals.

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