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Programmable self-assembly of three-dimensional nanostructures from 10(4) unique components

Nucleic acids (DNA and RNA) are widely used to construct nanoscale structures with ever increasing complexity(1–14) for possible applications in fields as diverse as structural biology, biophysics, synthetic biology and photonics. The nanostructures are formed through one-pot self-assembly, with ear...

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Autores principales: Ong, Luvena L., Hanikel, Nikita, Yaghi, Omar K., Grun, Casey, Strauss, Maximilian T., Bron, Patrick, Lai-Kee-Him, Josephine, Schueder, Florian, Wang, Bei, Wang, Pengfei, Kishi, Jocelyn Y., Myhrvold, Cameron A., Zhu, Allen, Jungmann, Ralf, Bellot, Gaetan, Ke, Yonggang, Yin, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786436/
https://www.ncbi.nlm.nih.gov/pubmed/29219968
http://dx.doi.org/10.1038/nature24648
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author Ong, Luvena L.
Hanikel, Nikita
Yaghi, Omar K.
Grun, Casey
Strauss, Maximilian T.
Bron, Patrick
Lai-Kee-Him, Josephine
Schueder, Florian
Wang, Bei
Wang, Pengfei
Kishi, Jocelyn Y.
Myhrvold, Cameron A.
Zhu, Allen
Jungmann, Ralf
Bellot, Gaetan
Ke, Yonggang
Yin, Peng
author_facet Ong, Luvena L.
Hanikel, Nikita
Yaghi, Omar K.
Grun, Casey
Strauss, Maximilian T.
Bron, Patrick
Lai-Kee-Him, Josephine
Schueder, Florian
Wang, Bei
Wang, Pengfei
Kishi, Jocelyn Y.
Myhrvold, Cameron A.
Zhu, Allen
Jungmann, Ralf
Bellot, Gaetan
Ke, Yonggang
Yin, Peng
author_sort Ong, Luvena L.
collection PubMed
description Nucleic acids (DNA and RNA) are widely used to construct nanoscale structures with ever increasing complexity(1–14) for possible applications in fields as diverse as structural biology, biophysics, synthetic biology and photonics. The nanostructures are formed through one-pot self-assembly, with early examples typically containing on the order of 10 unique DNA strands. The introduction of DNA origami(4), which uses many staple strands to fold one long scaffold strand into a desired structure, gave access to kilo- to mega-dalton nanostructures containing about 10(2) unique DNA strands(6,7,10,13) . Aiming for even larger DNA origami structures is in principle possible(15,16), but faces the challenge of having to manufacture and route an increasingly long scaffold strand. An alternative and in principle more readily scalable approach uses DNA brick assembly(8,9), which doesn’t need a scaffold and instead uses hundreds of short DNA brick strands that self-assemble according to specific inter-brick interactions. First-generation bricks used to create 3D structures are 32-nt long with four 8-nt binding domains that directed 10(2) distinct bricks into well-formed assemblies, but attempts to create larger structures encountered practical challenges and had limited success.(9) Here we show that a new generation of DNA bricks with longer binding domains makes it possible to self-assemble 0.1 – 1 giga-dalton three-dimensional nanostructures from 10(4) unique components, including a 0.5 giga-dalton cuboid containing 30,000 unique bricks and a 1 giga-dalton rotationally symmetric tetramer. We also assemble a cuboid containing 10,000 bricks and 20,000 uniquely addressable ‘nano-voxels’ that serves as a molecular canvas for three-dimensional sculpting, with introduction of sophisticated user-prescribed 3D cavities yielding structures such as letters, a complex helicoid and a teddy bear. We anticipate that, with further optimization, even larger assemblies might be accessible and prove useful as scaffolds or for positioning functional components.
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spelling pubmed-57864362018-06-06 Programmable self-assembly of three-dimensional nanostructures from 10(4) unique components Ong, Luvena L. Hanikel, Nikita Yaghi, Omar K. Grun, Casey Strauss, Maximilian T. Bron, Patrick Lai-Kee-Him, Josephine Schueder, Florian Wang, Bei Wang, Pengfei Kishi, Jocelyn Y. Myhrvold, Cameron A. Zhu, Allen Jungmann, Ralf Bellot, Gaetan Ke, Yonggang Yin, Peng Nature Article Nucleic acids (DNA and RNA) are widely used to construct nanoscale structures with ever increasing complexity(1–14) for possible applications in fields as diverse as structural biology, biophysics, synthetic biology and photonics. The nanostructures are formed through one-pot self-assembly, with early examples typically containing on the order of 10 unique DNA strands. The introduction of DNA origami(4), which uses many staple strands to fold one long scaffold strand into a desired structure, gave access to kilo- to mega-dalton nanostructures containing about 10(2) unique DNA strands(6,7,10,13) . Aiming for even larger DNA origami structures is in principle possible(15,16), but faces the challenge of having to manufacture and route an increasingly long scaffold strand. An alternative and in principle more readily scalable approach uses DNA brick assembly(8,9), which doesn’t need a scaffold and instead uses hundreds of short DNA brick strands that self-assemble according to specific inter-brick interactions. First-generation bricks used to create 3D structures are 32-nt long with four 8-nt binding domains that directed 10(2) distinct bricks into well-formed assemblies, but attempts to create larger structures encountered practical challenges and had limited success.(9) Here we show that a new generation of DNA bricks with longer binding domains makes it possible to self-assemble 0.1 – 1 giga-dalton three-dimensional nanostructures from 10(4) unique components, including a 0.5 giga-dalton cuboid containing 30,000 unique bricks and a 1 giga-dalton rotationally symmetric tetramer. We also assemble a cuboid containing 10,000 bricks and 20,000 uniquely addressable ‘nano-voxels’ that serves as a molecular canvas for three-dimensional sculpting, with introduction of sophisticated user-prescribed 3D cavities yielding structures such as letters, a complex helicoid and a teddy bear. We anticipate that, with further optimization, even larger assemblies might be accessible and prove useful as scaffolds or for positioning functional components. 2017-12-06 /pmc/articles/PMC5786436/ /pubmed/29219968 http://dx.doi.org/10.1038/nature24648 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Ong, Luvena L.
Hanikel, Nikita
Yaghi, Omar K.
Grun, Casey
Strauss, Maximilian T.
Bron, Patrick
Lai-Kee-Him, Josephine
Schueder, Florian
Wang, Bei
Wang, Pengfei
Kishi, Jocelyn Y.
Myhrvold, Cameron A.
Zhu, Allen
Jungmann, Ralf
Bellot, Gaetan
Ke, Yonggang
Yin, Peng
Programmable self-assembly of three-dimensional nanostructures from 10(4) unique components
title Programmable self-assembly of three-dimensional nanostructures from 10(4) unique components
title_full Programmable self-assembly of three-dimensional nanostructures from 10(4) unique components
title_fullStr Programmable self-assembly of three-dimensional nanostructures from 10(4) unique components
title_full_unstemmed Programmable self-assembly of three-dimensional nanostructures from 10(4) unique components
title_short Programmable self-assembly of three-dimensional nanostructures from 10(4) unique components
title_sort programmable self-assembly of three-dimensional nanostructures from 10(4) unique components
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5786436/
https://www.ncbi.nlm.nih.gov/pubmed/29219968
http://dx.doi.org/10.1038/nature24648
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