摘要
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.
| 源语言 | 英语 |
|---|---|
| 文章编号 | 201102 |
| 期刊 | Journal of Chemical Physics |
| 卷 | 158 |
| 期 | 20 |
| DOI | |
| 出版状态 | 已出版 - 28 5月 2023 |
| 已对外发布 | 是 |
指纹
探究 'An ultrafast phototrigger of the Trp5CN-Trp motif in a β -hairpin peptide' 的科研主题。它们共同构成独一无二的指纹。引用此
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