期刊
NATURE
卷 525, 期 7567, 页码 82-+出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/nature14860
关键词
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资金
- Engineering and Physical Sciences Research Council [EP/G037930/1, EP/P504287/1]
- Human Frontier Science Program [RGP0030/2013]
- Microsoft Research PhD Scholarship
- ERC Advanced Grant VERIWARE
- Royal Society-Wolfson Research Merit Award
- Biotechnology and Biological Sciences Research Council [BB/M005739/1] Funding Source: researchfish
- Engineering and Physical Sciences Research Council [GR/A10274/01, EP/G037930/1] Funding Source: researchfish
- BBSRC [BB/M005739/1] Funding Source: UKRI
- EPSRC [EP/G037930/1] Funding Source: UKRI
DNA origami is a robust assembly technique that folds a single-stranded DNA template into a target structure by annealing it with hundreds of short 'staple' strands(1-4.) Its guiding design principle is that the target structure is the single most stable configuration(5). The folding transition is cooperative(4,6,7) and, as in the case of proteins, is governed by information encoded in the polymer sequence(8-11). A typical origami folds primarily into the desired shape, but misfolded structures can kinetically trap the system and reduce the yield(2). Although adjusting assembly conditions(2,12) or following empirical design rules(12,13) can improve yield, well-folded origami often need to be separated from misfolded structures(2,3,14-16). The problem could in principle be avoided if assembly pathway and kinetics were fully understood and then rationally optimized. To this end, here we present a DNA origami system with the unusual property of being able to form a small set of distinguishable and well-folded shapes that represent discrete and approximately degenerate energy minima in a vast folding landscape, thus allowing us to probe the assembly process. The obtained high yield of well-folded origami structures confirms the existence of efficient folding pathways, while the shape distribution provides information about individual trajectories through the folding landscape. We find that, similarly to protein folding, the assembly of DNA origami is highly cooperative; that reversible bond formation is important in recovering from transient misfoldings; and that the early formation of long-range connections can very effectively enforce particular folds. We use these insights to inform the design of the system so as to steer assembly towards desired structures. Expanding the rational design process to include the assembly pathway should thus enable more reproducible synthesis, particularly when targeting more complex structures. We anticipate that this expansion will be essential if DNA origami is to continue its rapid development(1-3,17-19) and become a reliable manufacturing technology(20).
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