<p>Figure 3. Response of enzyme-functionalized GFETs to two nitriles.</p>
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<p>Figure 3a. Normalized response of wild-type QueF and QueF-Y5Y fusion protein to concentrations of preQ<sub>0</sub> to 500nM. Gray vertical lines represent approximate timings for analyte addition. Arrowed symbols: ● = sensor wash in phosphate buffer, ◆ = addition of 4 µM NADPH, ■ = addition of 1 M substrate. GFET conditions: <em>V</em><sub>g</sub>: 500 mV, <em>V</em><sub>d</sub>: 5 mV.</p>
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<p>Figure 3a. Normalized response of wild-type QueF and QueF-Y5Y fusion protein to concentrations benzyl cyanide (BnCN) to 500nM. Gray vertical lines represent approximate timings for analyte addition. Gray vertical lines represent approximate timings for analyte addition. Arrowed symbols: ● = sensor wash in phosphate buffer, ◆ = addition of 4 µM NADPH, ■ = addition of 1 M substrate. GFET conditions: <em>V</em><sub>g</sub>: 500 mV, <em>V</em><sub>d</sub>: 5 mV.</p>
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<p>Figure 3c. Normalized response curve fittings for each sample. Error bars ranges are mean ± standard deviation. Number of replicates are given in Table 1. Standard deviation in panel c is calculated from the pooled variance of all signals over 1 min.</p>
Funding
Manchester-Bangor DTP2
Biotechnology and Biological Sciences Research Council