Volume 59, Issue 6 pp. 2284-2288
Communication

Additive-Free Green Light-Induced Ligation Using BODIPY Triggers

Prof. Dr. Ming Li

Prof. Dr. Ming Li

School of Materials Science and Engineering, Central South University, Changsha, Hunan, 410083 China

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Prof. Dr. Andrew P. Dove

Prof. Dr. Andrew P. Dove

School of Chemistry, University of Birmingham, Edgbaston, Birmingham, B15 2TT UK

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Dr. Vinh X. Truong

Corresponding Author

Dr. Vinh X. Truong

Department of Materials Science and Engineering, Monash University, Clayton, VIC, 3800 Australia

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First published: 25 November 2019
Citations: 42

Graphical Abstract

Photochemical ligation between BODIPY thioether and propiolate, triggered by green light, enables formation of hydrogel and photo-patterning of bioactive molecules.

Abstract

Photochemical ligation is important in biomaterials engineering for spatiotemporal control of biochemical processes. Such reactions however generally require activation by high energy UV or short wavelength blue light, which can limit their use as a consequence of the potential of these high energy light sources to damage living cells. Herein, we present an additive-free, biocompatible, chemical ligation triggered by mild visible light. BODIPY dyes with a pendant thioether attached at the meso-position undergo photolysis of the [C−S] bond under green light (λ=530 nm) excitation, producing an ion pair intermediate that can react specifically with a propiolate group. The utility of this photochemical ligation in materials science is demonstrated by the fabrication of hydrogels with specific architectures, photo-immobilization of biomacromolecules, and live cell encapsulation within a hydrogel scaffold.

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