Abstract
Phototriggers are useful molecular tools to initiate reactions in enzymes by light for the purpose of photoenzymatic design and mechanistic investigations. Here, we incorporated the non-natural amino acid 5-cyanotryptophan (W5CN) in a polypeptide scaffold and resolved the photochemical reaction of the W5CN-W motif using femtosecond transient UV/Vis and mid-IR spectroscopy. We identified a marker band of ∼2037 cm-1 from the CN stretch of the electron transfer intermediate W5CN·- in the transient IR measurement and found UV/Vis spectroscopic evidence for the W·+ radical at 580 nm. Through kinetic analysis, we characterized that the charge separation between the excited W5CN and W occurs in 253 ps, with a charge-recombination lifetime of 862 ps. Our study highlights the potential use of the W5CN-W pair as an ultrafast phototrigger to initiate reactions in enzymes that are not light-sensitive, making downstream reactions accessible to femtosecond spectroscopic detection.
Cite
CITATION STYLE
Zhang, Q., Zhou, Z., Deng, B., Wang, B., Kang, X. W., Chen, J., … Zhong, D. (2023). An ultrafast phototrigger of the Trp5CN-Trp motif in a β -hairpin peptide. Journal of Chemical Physics, 158(20). https://doi.org/10.1063/5.0143384
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.