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利用红移快速弛豫偶氮苯对阴离子载体进行瞬态光活化

Transient Photoactivation of Anionophores by Using Redshifted Fast-Relaxing Azobenzenes.

作者信息

Kerckhoffs Aidan, Ahmad Manzoor, Langton Matthew J

机构信息

Department of Chemistry, Chemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford, OX1 3TA, UK.

出版信息

Chemistry. 2024 Nov 15;30(64):e202402382. doi: 10.1002/chem.202402382. Epub 2024 Oct 29.

Abstract

Photo-regulated transmembrane ionophores enable spatial and temporal control over activity, offering promise as targeted therapeutics. Key to such applications is control using bio-compatible visible light. Herein, we report red-shifted azobenzene-derived synthetic anionophores that use amber or red light to trigger (E)-(Z) photoisomerisation and activation of transmembrane chloride transport. We demonstrate that by tuning the thermal half-life of the more active, but thermodynamically unstable, Z isomer to relax on the timescale of minutes, transient activation of ion transport can be achieved by activating solely with visible light and deactivating by thermal relaxation.

摘要

光调节跨膜离子载体能够实现对活性的空间和时间控制,有望成为靶向治疗药物。此类应用的关键在于使用生物相容性可见光进行控制。在此,我们报道了红移的偶氮苯衍生合成阴离子载体,它们利用琥珀色或红光触发(E)-(Z)光异构化并激活跨膜氯转运。我们证明,通过将活性更高但热力学不稳定的Z异构体的热半衰期调节至在几分钟的时间尺度上弛豫,可以仅通过可见光激活并通过热弛豫失活来实现离子转运的瞬时激活。

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