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Chemical Modification of the Tryptophan Residue in a Recombinant Ca2+-ATPase N-domain for Studying Tryptophan-ANS FRET
Published on: October 9, 2021
Fabrication of a ratiometric fluorescence nanoprobe for detecting tryptophan enantiomers
Hui Heng1, Qingyang Gu1, Haibo Jin1
1College of New Materials and Chemical Engineering, Beijing Institute of Petrochemical Technology, Beijing, 102617, China; Beijing Key Laboratory of Fuels Cleaning and Advanced Catalytic Emission Reduction Technology, Beijing, 102617, China.
Abstract:
A novel ratiometric fluorescence nanoprobe was developed to detect tryptophan enantiomers with high selectivity and sensitivity. Fluorescein (FL) was doped into SiO2 nanoparticles with little dye leakage, acting as an internal reference signal. The chiral center of L-histidine (L-His) was introduced by partially replacing the carboxyl on the surface of SiO2. The response signal of Eu3+ was coordinated with carboxyl to obtain the FL@SiO2-Eu/His nanoprobe. The nanoprobe shows enantioselective luminescence responses for tryptophan enantiomers. The red emission of Eu3+ can be effectively quenched by the tryptophan enantiomers, but the quenching efficiency is different due to the different interactions with the chiral recognition sites. The fluorescence intensity ratio (I613/I515) shows excellent linearity with tryptophan enantiomers in the range of 0-100 μM (R2 > 0.99). The limit of detection (LOD) is 1.0 μM and 1.3 μM for L-tryptophan (L-Trp) and D-tryptophan (D-Trp), respectively. The FL@SiO2-Eu/His nanoprobe shows good selectivity and specific recognition in serum actual samples. In addition, the nanoprobe can realize visual detection under UV light due to the obvious color change. This work provides an innovative idea for the development of new probes in the detection field.
![Radiosynthesis of 1-2-[18F]Fluoroethyl-L-Tryptophan using a One-pot, Two-step Protocol](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F63025.jpg&w=3840&q=50)
