A Reversible Light‐Driven Biomimetic K+/Na+‐Exchanger Controls Cancer Cell Apoptosis

Author:

Wu Yaqi12,Li Cong12,Wu Yanliang1,Xu Jiayun1,Ni Zhigang1,Reany Ofer3,Yan Tengfei1,Zhu Dingcheng1,Liu Junqiu12ORCID

Affiliation:

1. College of Material Chemistry and Chemical Engineering Key Laboratory of Organosilicon Chemistry and Material Technology Ministry of Education Hangzhou Normal University Hangzhou 311121 China

2. College of Chemistry and Chemical Engineering Key Laboratory of Special Functional and Smart Polymer Materials of Ministry of Industry and Information Technology Northwestern Polytechnical University Xi'an 710129 China

3. Avinoam Adam Department of Natural Sciences Open University of Israel Ra'anana 4353701 Israel

Abstract

AbstractAlthough natural dual‐ion exchangers are indispensable for bio‐organic functions, developing their artificial counterparts remains nearly unexplored. Herein, this work proposes a novel light‐controlled K+/Na+‐transport‐exchanger TE12, realizing an unprecedented reversible switch between K+‐ and Na+‐transmembrane transport by changing its transport mechanism (channel and carrier). The conformational transformation of the azobenzene moiety in TE12 essentially induces this. The K+/Na+ selectivity of K+‐channel Trans‐TE12 is as high as 20.3, making it one of the most selective artificial K+‐transporters. Moreover, considering the scarcity of artificial Na+‐transporters, the Na+‐carrier Cis‐TE12 with high Na+/K+ selectivity (9.25) represents a breakthrough. Cis‐TE12 significantly triggers cell apoptosis by igniting fascinating “Na+ sparks” first observed on cancer cells treated with synthetic channels, while K+‐channel Trans‐TE12 exhibits low toxicity. Importantly, TE12 can function as a spatiotemporally controllable ion interference therapy, enabling in situ 365 nm light‐triggered and 450 nm light‐inhibited cell death. This work realizes sophisticated functions in a simplified structure by the “Less is More” design concept. It opens a shortcut toward the future iterative updating of artificial ion transporters to make them better biological analogs and therapeutic agents.

Funder

National Natural Science Foundation of China

National Key Research and Development Program of China

Publisher

Wiley

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