Isiah M. Warner acknowledges the National Science Foundation, the National Institutes of Health, and the Philip W. West Endowment for their support. Robert M. Strongin also acknowledges the National Institutes of Health for support via grant EB002044.
Macrocyclic compounds, Biochemistry -- Research, Amino acids
The spectroscopic properties of a chiral boronic acid based resorcinarene macrocycle employed for chiral analysis were investigated. Specifically, the emission and excitation characteristics of tetraarylboronate resorcinarene macrocycle (TBRM) and its quantum yield were evaluated. The chiral selector TBRM was investigated as a chiral reagent for the enantiomeric discrimination of amino acids using steady-state fluorescence spectroscopy. Chiral recognition of amino acids in the presence of the macrocycle was based on diastereomeric complexes. Results demonstrated that TBRM had better chiral discrimination ability for lysine as compared to the other amino acids. Partial least squares regression modeling (PLS-1) of spectral data for macrocycle-lysine guest-host complexes was used to correlate the changes in the fluorescence emission for a set of calibration samples consisting of TBRM in the presence of varying enantiomeric compositions of lysine. In addition, validation studies were performed using an independently prepared set of samples with different enantiomeric compositions of lysine. The results of multivariate regression modeling indicated good prediction ability of lysine, which was confirmed by a root mean square percent relative error (RMS%RE) of 5.8%.
Richard, Gerald I.; Marwani, Hadi M.; Jiang, Shan; Fakayode, Sayo O.; Lowry, Mark; Strongin, Robert M.; and Warner, Isiah M., "Chiral Recognition of Amino Acids by Use of a Fluorescent Resorcinarene" (2008). Chemistry Faculty Publications and Presentations. 62.