Skip to main content
. Author manuscript; available in PMC: 2020 Feb 1.
Published in final edited form as: J Neurosci Res. 2019 May 20;97(8):946–960. doi: 10.1002/jnr.24433

Figure 1. Sensor design and characterization.

Figure 1.

(A) Top, schematic representation of the glucose sensor. Abbreviations indicate the N-terminal pRSET affinity tag sequence (Nt), the glucose-binding protein (TtGBP) and the circularly-permuted T-Sapphire (cpmTS). Bottom, the full sequence of the sensor as reported in Díaz-García et al. (2017), highlighting each domain with the same color code from the schematic representation. (B) Excitation and emission spectra of the purified sensor protein. (C) Dose-response curves at different pH values. Data points and whiskers represent the mean and the range of duplicate measurements, respectively. The curves represent the best fit to a Hill equation (see Eq. 1 in Methods). Experiments were performed at room temperature of approximately 22°C.