Engineering of Multivalent Membrane‐Anchored DNA Frameworks for Precise Profiling of Variable Membrane Permeability During Reversible Electroporation

Author:

Liu Yixin1,Fan Zihui1,Xiang Xiao‐Wei2,Tao Xiaonan3,Xia Xinwei1,Shi Qian1,Lu Yanwei1,Lu Jiayin1,Gu Hongzhou1,Liu Yan‐Jun1ORCID,Liu Baohong1ORCID

Affiliation:

1. Department of Chemistry Shanghai Stomatological Hospital State Key Lab of Molecular Engineering of Polymers Shanghai Xuhui Central Hospital Zhongshan‐Xuhui Hospital Shanghai Key Laboratory of Medical Epigenetics Institutes of Biomedical Sciences Fudan University Shanghai 200032 China

2. Westlake Laboratory of Life Sciences and Biomedicine School of Life Sciences Westlake University Hangzhou Zhejiang 310030 China

3. School of Information Science and Technology Fudan University Shanghai 200032 China

Abstract

AbstractElectroporation techniques have emerged as attractive tools for intracellular delivery, rendering promising prospects towards clinical therapies. Transient disruption of membrane permeability is the critical process for efficient electroporation‐based cargo delivery. However, smart nanotools for precise characterization of transient membrane changes induced by strong electric pulses are extremely limited. Herein, multivalent membrane‐anchored fluorescent nanoprobes (MMFNPs) that take advantages of flexible functionalization and spatial arrangement of DNA frameworks are developed for in situ evaluation of electric field‐induced membrane permeability during reversible electroporation . Single‐molecule fluorescence imaging techniques are adopted to precisely  verify the excellent analytical performance of the engineered MMFNPs. Benefited from tight membrane anchoring and sensitive adenosine triphosphate (ATP) profiling, varying degrees of membrane disturbances are visually exhibited under different intensities of the microsecond pulse electric field (µsPEF). Significantly, the dynamic process of membrane repair during reversible electroporation is well demonstrated via ATP fluctuations monitored by the designed MMFNPs. Furthermore, molecular dynamics (MD) simulations are performed for accurate verification of electroporation‐driven dynamic cargo entry via membrane nanopores. This work provides an avenue for effectively capturing transient fluctuations of membrane permeability under external stimuli, offering valuable guidance for developing efficient and safe electroporation‐driven delivery strategies for clinical diagnosis and therapeutics.

Funder

National Basic Research Program of China

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Publisher

Wiley

Subject

General Materials Science,General Chemistry

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