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作 者:Yingying Chen Mingzhu Yan Yushi Wang Jinhua Shang Shizhen He Yuhui Gao Chen Hong Xiaoqing Liu Fuan Wang
机构地区:[1]College of Chemistry and Molecular Sciences,Wuhan University,Wuhan 430072
出 处:《CCS Chemistry》2023年第7期1697-1708,共12页中国化学会会刊(英文)
基 金:This work was supported by the National Natural Science Foundation of China(grant nos.21874103 and 22074112);the Fundamental Research Funds for the Central Universities(grant no.2042022kf1175);the Central Funds Guiding the Local Science and Technology Development of Shenzhen(grant no.2021Szvup101).
摘 要:Synthetic DNA motors have spurred considerable research interest as a way to interrogate biochemical processes that can further facilitate disease diagnosis.However,current direct sense-on-demand DNA motors are hampered by undesired signal leakage originating from their nonspecific stimulation prior to their arrival at target sites.Herein,we propose a DNAzyme-guided DNA amplification motor through the facile built-in of a stimuli-responsive DNAzyme brake to facilitate the in vivo sensitive imaging of biomarkers by minimizing the off-site signal leakage in living systems.To realize the on-site activation,the inactive DNAzyme DNA motor was encapsulated into the folate(FA)-modified zeolitic imidazolate framework-8(ZIF-8)/poly(D,L-lactic-co-glycolic acid(PLGA)nanovesicles.The FA interaction-promoted tumor-cell-selective delivery and the pH-responsive disassembly of ZIF-8/PLGA permitted sufficient release of DNAzyme cofactors to achieve on-site stimulation of DNAzyme for restoring the temporally caged DNA amplification motor in tumor cells where the endogenous miRNA target was thus specifically and sensitively analyzed.By integration of the cellselective delivery and the site-specific stimulation,our DNAzyme-guided DNA motor can realize the reliable imaging of tumor cells and provide a new toolbox for disease diagnosis.
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