New York University Abu Dhabi , P.O. Box 129188, Abu Dhabi, United Arab Emirates.
Department of Chemistry, The University of Hong Kong , Pokfulam Road, Hong Kong 999077, People's Republic of China.
J Am Chem Soc. 2017 Sep 13;139(36):12591-12600. doi: 10.1021/jacs.7b06363. Epub 2017 Aug 29.
Representative tertiary amines were linked to the 8-cyano-7-hydroxyquinolinyl (CyHQ) photoremovable protecting group (PPG) to create photoactivatable forms suitable for use in studying cell physiology. The photoactivation of tamoxifen and 4-hydroxytamoxifen, which can be used to activate Cre recombinase and CRISPR-Cas9 gene editing, demonstrated that highly efficient release of bioactive molecules could be achieved through one- and two-photon excitation (1PE and 2PE). CyHQ-protected anilines underwent a photoaza-Claisen rearrangement instead of releasing amines. Time-resolved spectroscopic studies revealed that photorelease of the tertiary amines was extremely fast, occurring from a singlet excited state of CyHQ on the 70 ps time scale.
代表性的叔胺与 8-氰基-7-羟基喹啉基(CyHQ)光脱保护基团(PPG)连接,形成适用于研究细胞生理学的光活化形式。他莫昔芬和 4-羟基他莫昔芬的光活化可用于激活 Cre 重组酶和 CRISPR-Cas9 基因编辑,证明通过单光子和双光子激发(1PE 和 2PE)可以实现生物活性分子的高效释放。CyHQ 保护的苯胺经历光氮杂-Claisen 重排而不是释放胺。时间分辨光谱研究表明,叔胺的光释放非常快,从 CyHQ 的单重激发态在 70 ps 的时间尺度上发生。