DNA-Based Dynamic Mimicry of Membrane Proteins for Programming Adaptive Cellular Interactions

被引:95
|
作者
Li, Jin [1 ,2 ]
Xun, Kanyu [2 ]
Zheng, Liyan [2 ]
Peng, Xueyu [2 ]
Qiu, Liping [2 ]
Tan, Weihong [2 ,3 ,4 ]
机构
[1] Chinese Acad Sci, Univ Chinese Acad Sci, Inst Basic Med & Canc IBMC, Canc Hosp, Hangzhou 310022, Zhejiang, Peoples R China
[2] Hunan Univ, Coll Chem & Chem Engn, Aptamer Engn Ctr Hunan Prov, Coll Biol,Mol Sci & Biomed Lab MBL,State Key Lab, Changsha 410082, Hunan, Peoples R China
[3] Shanghai Jiao Tong Univ, Renji Hosp, Inst Mol Med IMM, Sch Med,State Key Lab Oncogenes & Related Genes, Shanghai 200240, Peoples R China
[4] Shanghai Jiao Tong Univ, Coll Chem & Chem Engn, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
D O I
10.1021/jacs.0c11245
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cells sense and respond to the external environment, mainly through proteins presented on the membrane where their expression and conformation are dynamically regulated via intracellular programs. Here, we engineer a cell-surface nanoarchitecture that realizes molecular-recognition-initiated DNA assembly to mimic the dynamic behavior of membrane proteins, enabling the manipulation of cellular interaction in response to environmental changes. Our results show that this membrane-anchored DNA nanoarchitecture can be specifically activated by cell-responsive signals to external stimulation. Accordingly, multiple functional modules can be assembled onto the membrane to equip the cell with cell-type-specific binding and killing. This system is expected to offer a new paradigm for engineering therapeutic cells with customized sensing/response pathways.
引用
收藏
页码:4585 / 4592
页数:8
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