DNA Origami as Scaffolds for Self-Assembly of Lipids and Proteins

被引:18
作者
Dong, Yuanchen [1 ,2 ,4 ]
Mao, Youdong [1 ,2 ,3 ]
机构
[1] Harvard Med Sch, Dept Microbiol, Dana Farber Canc Inst, Dept Canc Immunol & Virol, 450 Brookline Ave, Boston, MA 02215 USA
[2] Dana Farber Canc Inst, Intel Parallel Comp Ctr Struct Biol, 450 Brookline Ave, Boston, MA 02215 USA
[3] Peking Univ, Ctr Quantitat Biol, Sch Phys, State Key Lab Artificial Microstruct & Mesoscop P, Beijing 100871, Peoples R China
[4] Chinese Acad Sci, Inst Chem, CAS Key Lab Colloid Interfaces & Chem Thermodynam, 2 Zhongguancun Beiyijie, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
DNA origami; lipids; nanotechnology; proteins; self-assembly; CRYO-EM STRUCTURE; FOLDING DNA; STRANDED-DNA; NANOSTRUCTURES; VIRUS; LIPOSOMES; SHAPES;
D O I
10.1002/cbic.201900073
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Since first being reported in 2006, the DNA origami approach has attracted increasing attention due to programmable shapes, structural stability, biocompatibility, and fantastic addressability. Herein, we provide an account of recent developments of DNA origami as scaffolds for templating the selfassembly of distinct biocomponents, essentially proteins and lipids, into a diverse spectrum of integrated supramolecular architectures. First, the historical development of the DNA origami concept is briefly reviewed. Next, various applications of DNA origami constructs in controllable directed assembly of soluble proteins are discussed. The manipulation and self-assembly of lipid membranes and membrane proteins by using DNA origami as scaffolds are also addressed. Furthermore, recent progress in applying DNA origami in cryoelectron microscopy analysis is discussed. These advances collectively emphasize that the DNA origami approach is a highly versatile, fast evolving tool that may be integrated with lipids and proteins in a way that meets future challenges in molecular biology and nanomedicine.
引用
收藏
页码:2422 / 2431
页数:10
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