DNA Framework-Based Topological Cell Sorters

被引:42
|
作者
Yin, Fangfei [1 ,2 ]
Li, Min [3 ,4 ]
Mao, Xiuhai [3 ,4 ]
Li, Fan [3 ,4 ]
Xiang, Xuelin [3 ,4 ]
Li, Qian [3 ,4 ]
Wang, Lihua [1 ,2 ,5 ,6 ]
Zuo, Xiaolei [3 ,4 ]
Fan, Chunhai [3 ,4 ]
Zhu, Ying [1 ,2 ,5 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Appl Phys, Div Phys Biol, CAS Key Lab Interfacial Phys & Technol, Shanghai 201800, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Shanghai Jiao Tong Univ, Renji Hosp, Sch Med, Inst Mol Med, Shanghai 200127, Peoples R China
[4] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Frontiers Sci Ctr Transformat Mol, Shanghai 200127, Peoples R China
[5] Chinese Acad Sci, Shanghai Adv Res Inst, Shanghai 201210, Peoples R China
[6] East China Normal Univ, Sch Chem & Mol Engn, Shanghai Key Lab Green Chem & Chem Proc, Shanghai 200241, Peoples R China
基金
中国国家自然科学基金;
关键词
cell sorting; DNA nanostructures; framework nucleic acid; topological engineering; NANOSTRUCTURES; INTEGRIN; FORCES; TCR;
D O I
10.1002/anie.202002020
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Molecular recognition in cell biological process is characterized with specific locks-and-keys interactions between ligands and receptors, which are ubiquitously distributed on cell membrane with topological clustering. Few topologically-engineered ligand systems enable the exploration of the binding strength between ligand-receptor topological organization. Herein, we generate topologically controlled ligands by developing a family of tetrahedral DNA frameworks (TDFs), so the multiple ligands are stoichiometrically and topologically arranged. This topological control of multiple ligands changes the nature of the molecular recognition by inducing the receptor clustering, so the binding strength is significantly improved (ca. 10-fold). The precise engineering of topological complexes formed by the TDFs are readily translated into effective binding control for cell patterning and binding strength control of cells for cell sorting. This work paves the way for the development of versatile design of topological ligands.
引用
收藏
页码:10406 / 10410
页数:5
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