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1.
Nanoscale ; 15(17): 7772-7780, 2023 May 04.
Artigo em Inglês | MEDLINE | ID: mdl-37057647

RESUMO

Hierarchical self-assembly of nanostructures with addressable complexity has been a promising route for realizing novel functional materials. Traditionally, the fabrication of such structures on a large scale has been achievable using top-down methods but with the cost of complexity of the fabrication equipment versus resolution and limitation mainly to 2D structures. More recently bottom-up methods using molecules like DNA have gained attention due to the advantages of low fabrication costs, high resolution and simplicity in an extension of the methods to the third dimension. One of the more promising bottom-up techniques is DNA origami due to the robust self-assembly of arbitrarily shaped nanostructures with feature sizes down to a few nanometers. Here, we show that under specific ionic conditions of the buffer, the employed plus-shaped, blunt-ended Seeman tile (ST) origami forms elongated, ordered 2D lattices, which are further rolled into 3D tubes in solution. Imaging structures on a surface by atomic force microscopy reveals ribbon-like structures, with single or double layers of the origami lattice. Further studies of the double-layered structures in a liquid state by confocal microscopy and cryo-TEM revealed elongated tube structures with a relatively uniform width but with a varying length. Through meticulous study, we concluded that the assembly process of these 3D DNA origami tubes is heavily dependent on the concentration of both mono- and divalent cations. In particular, nickel seems to act as a trigger for the formation of the tubular assemblies in liquid.


Assuntos
Nanoestruturas , Nanotecnologia , Nanotecnologia/métodos , Conformação de Ácido Nucleico , DNA/química , Nanoestruturas/química , Microscopia de Força Atômica
2.
Nanoscale ; 15(7): 3212-3218, 2023 Feb 16.
Artigo em Inglês | MEDLINE | ID: mdl-36722916

RESUMO

The DNA origami technique offers precise positioning of nanoscale objects with high accuracy. This has facilitated the development of DNA origami-based functional nanomechanical devices that enable the investigation of DNA-protein interactions at the single particle level. Herein, we used the DNA origami technique to fabricate a nanoscale device for studying DNA bending proteins. For a proof of concept, we used TATA-box binding protein (TBP) to evaluate our approach. Upon binding to the TATA box, TBP causes a bend to DNA of ∼90°. Our device translates this bending into an angular change that is readily observable with a conventional transmission electron microscope (TEM). Furthermore, we investigated the roles of transcription factor II A (TF(II)A) and transcription factor II B (TF(II)B). Our results indicate that TF(II)A introduces additional bending, whereas TF(II)B does not significantly alter the TBP-DNA structure. Our approach can be readily adopted to a wide range of DNA-bending proteins and will aid the development of DNA-origami-based devices tailored for the investigation of DNA-protein interactions.


Assuntos
Proteínas de Ligação a DNA , DNA , Proteína de Ligação a TATA-Box/genética , Proteína de Ligação a TATA-Box/metabolismo , Conformação de Ácido Nucleico , Proteínas de Ligação a DNA/química , DNA/química , Microscopia Eletrônica de Transmissão
3.
Bioconjug Chem ; 34(1): 6-17, 2023 01 18.
Artigo em Inglês | MEDLINE | ID: mdl-35984467

RESUMO

Since its discovery in 2006, the DNA origami technique has revolutionized bottom-up nanofabrication. This technique is simple yet versatile and enables the fabrication of nanostructures of almost arbitrary shapes. Furthermore, due to their intrinsic addressability, DNA origami structures can serve as templates for the arrangement of various nanoscale components (small molecules, proteins, nanoparticles, etc.) with controlled stoichiometry and nanometer-scale precision, which is often beyond the reach of other nanofabrication techniques. Despite the multiple benefits of the DNA origami technique, its applicability is often restricted by the limited stability in application-specific conditions. This Review provides an overview of the strategies that have been developed to improve the stability of DNA-origami-based assemblies for potential biomedical, nanofabrication, and other applications.


Assuntos
Nanopartículas , Nanoestruturas , DNA/química , Nanoestruturas/química , Conformação de Ácido Nucleico , Nanotecnologia/métodos
4.
Anal Chem ; 94(50): 17577-17586, 2022 12 20.
Artigo em Inglês | MEDLINE | ID: mdl-36480745

RESUMO

Reliable characterization of binding affinities is crucial for selected aptamers. However, the limited repertoire of universal approaches to obtain the dissociation constant (KD) values often hinders the further development of aptamer-based applications. Herein, we present a competitive hybridization-based strategy to characterize aptamers using DNA origami-based chiral plasmonic assemblies as optical reporters. We incorporated aptamers and partial complementary strands blocking different regions of the aptamers into the reporters and measured the kinetic behaviors of the target binding to gain insights on aptamers' functional domains. We introduced a reference analyte and developed a thermodynamic model to obtain a relative dissociation constant of an aptamer-target pair. With this approach, we characterized RNA and DNA aptamers binding to small molecules with low and high affinities.


Assuntos
Aptâmeros de Nucleotídeos , Aptâmeros de Nucleotídeos/química , RNA/química , DNA/química , Sondas de DNA/química , Hibridização de Ácido Nucleico , Técnica de Seleção de Aptâmeros
5.
ACS Nano ; 16(10): 16608-16616, 2022 10 25.
Artigo em Inglês | MEDLINE | ID: mdl-36178116

RESUMO

We address the problem of de novo design and synthesis of nucleic acid nanostructures, a challenge that has been considered in the area of DNA nanotechnology since the 1980s and more recently in the area of RNA nanotechnology. Toward this goal, we introduce a general algorithmic design process and software pipeline for rendering 3D wireframe polyhedral nanostructures in single-stranded RNA. To initiate the pipeline, the user creates a model of the desired polyhedron using standard 3D graphic design software. As its output, the pipeline produces an RNA nucleotide sequence whose corresponding RNA primary structure can be transcribed from a DNA template and folded in the laboratory. As case examples, we design and characterize experimentally three 3D RNA nanostructures: a tetrahedron, a triangular bipyramid, and a triangular prism. The design software is openly available and also provides an export of the targeted 3D structure into the oxDNA molecular dynamics simulator for easy simulation and visualization.


Assuntos
Nanoestruturas , RNA , Conformação de Ácido Nucleico , Nanotecnologia , Nanoestruturas/química , DNA/química
7.
Langmuir ; 38(9): 2954-2960, 2022 03 08.
Artigo em Inglês | MEDLINE | ID: mdl-35212547

RESUMO

Aptamers have emerged as versatile affinity ligands and as promising alternatives to protein antibodies. However, the inconsistency in the reported affinities and specificities of aptamers has greatly hindered the development of aptamer-based applications. Herein, we present a strategy to characterize aptamers by using DNA origami-based chiral plasmonic assemblies as reporters and establishing a competitive hybridization reaction-based thermodynamic model. We demonstrate the characterization of several DNA aptamers, including aptamers for small molecules and macromolecules, as well as aptamers with high and low affinities. The presented characterization scheme can be readily adapted to a wide selection of aptamers. We anticipate that our approach will advance the development of aptamer-based applications by enabling reliable and reproducible characterization of aptamers.


Assuntos
Aptâmeros de Nucleotídeos , Técnica de Seleção de Aptâmeros , Aptâmeros de Nucleotídeos/metabolismo , DNA , Ligantes
8.
Angew Chem Int Ed Engl ; 60(11): 5859-5863, 2021 03 08.
Artigo em Inglês | MEDLINE | ID: mdl-33320988

RESUMO

DNA nanotechnology offers a versatile toolbox for precise spatial and temporal manipulation of matter on the nanoscale. However, rendering DNA-based systems responsive to light has remained challenging. Herein, we describe the remote manipulation of native (non-photoresponsive) chiral plasmonic molecules (CPMs) using light. Our strategy is based on the use of a photoresponsive medium comprising a merocyanine-based photoacid. Upon exposure to visible light, the medium decreases its pH, inducing the formation of DNA triplex links, leading to a spatial reconfiguration of the CPMs. The process can be reversed simply by turning the light off and it can be repeated for multiple cycles. The degree of the overall chirality change in an ensemble of CPMs depends on the CPM fraction undergoing reconfiguration, which, remarkably, depends on and can be tuned by the intensity of incident light. Such a dynamic, remotely controlled system could aid in further advancing DNA-based devices and nanomaterials.

9.
ACS Nano ; 13(12): 13615-13619, 2019 12 24.
Artigo em Inglês | MEDLINE | ID: mdl-31808671

RESUMO

Understanding how the geometrical property of chirality is transferred into the physical properties of chiral materials is becoming increasingly important in various research fields, including plasmonics. Advances in DNA nanotechnology, especially DNA origami techniques, have enabled routine fabrication of complex chiral plasmonic assemblies. However, most of the work undertaken to date has involved plasmonic enantiomers. The concept of multiple chiral centers in stereochemistry provides simple guidelines for generating multiple chiral configurations beyond enantiomers. In this issue of ACS Nano, Wang et al. report DNA origami-based assembly and characterization of reconfigurable plasmonic chiral stereoisomers with up to three chiral centers. In this Perspective, we explore the implication of these results for further development of functional chiral plasmonic systems.


Assuntos
DNA/química , Ouro/química , Nanopartículas Metálicas/química , Conformação de Ácido Nucleico , Estereoisomerismo
10.
Sci Adv ; 5(11): eaax6023, 2019 11.
Artigo em Inglês | MEDLINE | ID: mdl-31819901

RESUMO

Coordinating functional parts to operate in concert is essential for machinery. In gear trains, meshed gears are compactly interlocked, working together to impose rotation or translation. In photosynthetic systems, a variety of biological entities in the thylakoid membrane interact with each other, converting light energy into chemical energy. However, coordinating individual parts to carry out regulated and coordinated motion within an artificial nanoarchitecture poses challenges, owing to the requisite control on the nanoscale. Here, we demonstrate DNA-directed nanosystems, which comprise hierarchically-assembled DNA origami filaments, fluorophores, and gold nanocrystals. These individual building blocks can execute independent, synchronous, or joint motion upon external inputs. These are optically monitored in situ using fluorescence spectroscopy, taking advantage of the sensitive distance-dependent interactions between the gold nanocrystals and fluorophores positioned on the DNA origami. Our work leverages the complexity of DNA-based artificial nanosystems with tailored dynamic functionality, representing a viable route towards technomimetic nanomachinery.


Assuntos
DNA/química , Movimento (Física) , Nanoestruturas , Nanotecnologia , Algoritmos , Ouro , Nanopartículas Metálicas , Modelos Teóricos , Nanoestruturas/química , Nanoestruturas/ultraestrutura
11.
J Vis Exp ; (145)2019 03 05.
Artigo em Inglês | MEDLINE | ID: mdl-30907870

RESUMO

The inherent addressability of DNA origami structures makes them ideal templates for the arrangement of metal nanoparticles into complex plasmonic nanostructures. The high spatial precision of a DNA origami-templated assembly allows controlling the coupling between plasmonic resonances of individual particles and enables tailoring optical properties of the constructed nanostructures. Recently, chiral plasmonic systems attracted a lot of attention due to the strong correlation between the spatial configuration of plasmonic assemblies and their optical responses (e.g., circular dichroism [CD]). In this protocol, we describe the whole workflow for the generation of DNA origami-based chiral assemblies of gold nanorods (AuNRs). The protocol includes a detailed description of the design principles and experimental procedures for the fabrication of DNA origami templates, the synthesis of AuNRs, and the assembly of origami-AuNR structures. In addition, the characterization of structures using transmission electron microscopy (TEM) and CD spectroscopy is included. The described protocol is not limited to chiral configurations and can be adapted for the construction of various plasmonic architectures.


Assuntos
DNA/química , Ouro/química , Nanotubos/química , Conformação de Ácido Nucleico , Dicroísmo Circular , Nanopartículas Metálicas/química , Nanotubos/ultraestrutura , Temperatura , Fatores de Tempo
12.
ACS Appl Mater Interfaces ; 10(51): 44221-44225, 2018 Dec 26.
Artigo em Inglês | MEDLINE | ID: mdl-30525378

RESUMO

Accurate and reliable biosensing is crucial for environmental monitoring, food safety, and diagnostics. Spatially reconfigurable DNA origami nanostructures are excellent candidates for the generation of custom sensing probes. Here we present a nanoscale biosensing device that combines the accuracy and precision of the DNA origami nanofabrication technique, unique optical responses of chiral plasmonic assemblies, and high affinity and selectivity of aptamers. This combination enables selective and sensitive detection of targets even in strongly absorbing fluids. We expect that the presented sensing scheme can be adapted to a wide range of analytes and tailored to specific needs.


Assuntos
Técnicas Biossensoriais/métodos , DNA/química , Ouro/química , Nanopartículas Metálicas/química
13.
ACS Photonics ; 5(4): 1151-1163, 2018 Apr 18.
Artigo em Inglês | MEDLINE | ID: mdl-30271812

RESUMO

The specificity and simplicity of the Watson-Crick base pair interactions make DNA one of the most versatile construction materials for creating nanoscale structures and devices. Among several DNA-based approaches, the DNA origami technique excels in programmable self-assembly of complex, arbitrary shaped structures with dimensions of hundreds of nanometers. Importantly, DNA origami can be used as templates for assembly of functional nanoscale components into three-dimensional structures with high precision and controlled stoichiometry. This is often beyond the reach of other nanofabrication techniques. In this Perspective, we highlight the capability of the DNA origami technique for realization of novel nanophotonic systems. First, we introduce the basic principles of designing and fabrication of DNA origami structures. Subsequently, we review recent advances of the DNA origami applications in nanoplasmonics, single-molecule and super-resolution fluorescent imaging, as well as hybrid photonic systems. We conclude by outlining the future prospects of the DNA origami technique for advanced nanophotonic systems with tailored functionalities.

14.
Angew Chem Int Ed Engl ; 57(41): 13495-13498, 2018 10 08.
Artigo em Inglês | MEDLINE | ID: mdl-30084527

RESUMO

Detecting small sequences of RNA in biological samples such as microRNA or viral RNA demands highly sensitive and specific methods. Here, a reconfigurable DNA origami template has been used where a chiral arrangement of gold nanorods on the structure can lead to the generation of strong circular dichroism (CD). Switching of the cross-like DNA structure is achieved by the addition of nucleic acid sequences, which arrests the structure in one of the possible chiral states by specific molecular recognition. A specific sequence can thus be detected through the resulting changes in the plasmonic CD spectrum. We show the sensitive and selective detection of a target RNA sequence from the hepatitis C virus genome. The RNA binds to a complementary sequence that is part of the lock mechanism, which leads to the formation of a defined state of the plasmonic system with a distinct optical response. With this approach, we were able to detect this specific RNA sequence at concentrations as low as 100 pm.


Assuntos
RNA Viral/análise , Dicroísmo Circular , DNA/química , Hepacivirus/genética , Limite de Detecção , Microscopia Eletrônica de Transmissão , Conformação de Ácido Nucleico , Estereoisomerismo
15.
Nat Commun ; 9(1): 1454, 2018 04 13.
Artigo em Inglês | MEDLINE | ID: mdl-29654323

RESUMO

Sliding is one of the fundamental mechanical movements in machinery. In macroscopic systems, double-rack pinion machines employ gears to slide two linear tracks along opposite directions. In microscopic systems, kinesin-5 proteins crosslink and slide apart antiparallel microtubules, promoting spindle bipolarity and elongation during mitosis. Here we demonstrate an artificial nanoscopic analog, in which gold nanocrystals can mediate coordinated sliding of two antiparallel DNA origami filaments powered by DNA fuels. Stepwise and reversible sliding along opposite directions is in situ monitored and confirmed using fluorescence spectroscopy. A theoretical model including different energy transfer mechanisms is developed to understand the observed fluorescence dynamics. We further show that such sliding can also take place in the presence of multiple DNA sidelocks that are introduced to inhibit the relative movements. Our work enriches the toolbox of DNA-based nanomachinery, taking one step further toward the vision of molecular nanofactories.


Assuntos
DNA/química , Nanopartículas Metálicas/química , Nanopartículas/química , Reagentes de Ligações Cruzadas , Transferência Ressonante de Energia de Fluorescência , Ouro/química , Cinesinas/química , Microscopia Eletrônica de Transmissão , Microtúbulos/química , Conformação de Ácido Nucleico , Propriedades de Superfície
16.
Sci Adv ; 3(4): e1602803, 2017 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-28439556

RESUMO

Selective configuration control of plasmonic nanostructures using either top-down or bottom-up approaches has remained challenging in the field of active plasmonics. We demonstrate the realization of DNA-assembled reconfigurable plasmonic metamolecules, which can respond to a wide range of pH changes in a programmable manner. This programmability allows for selective reconfiguration of different plasmonic metamolecule species coexisting in solution through simple pH tuning. This approach enables discrimination of chiral plasmonic quasi-enantiomers and arbitrary tuning of chiroptical effects with unprecedented degrees of freedom. Our work outlines a new blueprint for implementation of advanced active plasmonic systems, in which individual structural species can be programmed to perform multiple tasks and functions in response to independent external stimuli.

17.
Nat Commun ; 7: 10591, 2016 Feb 02.
Artigo em Inglês | MEDLINE | ID: mdl-26830310

RESUMO

Nature has developed striking light-powered proteins such as bacteriorhodopsin, which can convert light energy into conformational changes for biological functions. Such natural machines are a great source of inspiration for creation of their synthetic analogues. However, synthetic molecular machines typically operate at the nanometre scale or below. Translating controlled operation of individual molecular machines to a larger dimension, for example, to 10-100 nm, which features many practical applications, is highly important but remains challenging. Here we demonstrate a light-driven plasmonic nanosystem that can amplify the molecular motion of azobenzene through the host nanostructure and consequently translate it into reversible chiroptical function with large amplitude modulation. Light is exploited as both energy source and information probe. Our plasmonic nanosystem bears unique features of optical addressability, reversibility and modulability, which are crucial for developing all-optical molecular devices with desired functionalities.

18.
Nat Mater ; 13(9): 862-6, 2014 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-24997737

RESUMO

A reconfigurable plasmonic nanosystem combines an active plasmonic structure with a regulated physical or chemical control input. There have been considerable efforts on integration of plasmonic nanostructures with active platforms using top-down techniques. The active media include phase-transition materials, graphene, liquid crystals and carrier-modulated semiconductors, which can respond to thermal, electrical and optical stimuli. However, these plasmonic nanostructures are often restricted to two-dimensional substrates, showing desired optical response only along specific excitation directions. Alternatively, bottom-up techniques offer a new pathway to impart reconfigurability and functionality to passive systems. In particular, DNA has proven to be one of the most versatile and robust building blocks for construction of complex three-dimensional architectures with high fidelity. Here we show the creation of reconfigurable three-dimensional plasmonic metamolecules, which execute DNA-regulated conformational changes at the nanoscale. DNA serves as both a construction material to organize plasmonic nanoparticles in three dimensions, as well as fuel for driving the metamolecules to distinct conformational states. Simultaneously, the three-dimensional plasmonic metamolecules can work as optical reporters, which transduce their conformational changes in situ into circular dichroism changes in the visible wavelength range.


Assuntos
DNA/química , Nanoestruturas/química , Nanotecnologia/métodos , Modelos Moleculares , Conformação de Ácido Nucleico
19.
Nanoscale ; 6(16): 9331-8, 2014 Aug 21.
Artigo em Inglês | MEDLINE | ID: mdl-24740255

RESUMO

Recent advances in design and fabrication of helical nanostructures based on DNA self-assembly are reviewed. These helical nanostructures are either constructed entirely by DNA or based on DNA guided metal nanoparticles self-assembly. Biophysical properties and optical responses of corresponding helical nanostructures are also discussed.


Assuntos
DNA , Nanopartículas Metálicas , Nanoestruturas , Nanotecnologia/métodos , Conformação de Ácido Nucleico , DNA/química , DNA/ultraestrutura , Nanopartículas Metálicas/química , Nanopartículas Metálicas/ultraestrutura , Modelos Moleculares , Nanoestruturas/química , Nanoestruturas/ultraestrutura
20.
Nano Lett ; 14(3): 1627-33, 2014 Mar 12.
Artigo em Inglês | MEDLINE | ID: mdl-24517269

RESUMO

The combination of molecular self-assembly based on the DNA origami technique with lithographic patterning enables the creation of hierarchically ordered nanosystems, in which single molecules are positioned at precise locations on multiple length scales. Based on a hybrid assembly protocol utilizing DNA self-assembly and electron-beam lithography on transparent glass substrates, we here demonstrate a DNA origami microarray, which is compatible with the requirements of single molecule fluorescence and super-resolution microscopy. The spatial arrangement allows for a simple and reliable identification of single molecule events and facilitates automated read-out and data analysis. As a specific application, we utilize the microarray to characterize the performance of DNA strand displacement reactions localized on the DNA origami structures. We find considerable variability within the array, which results both from structural variations and stochastic reaction dynamics prevalent at the single molecule level.


Assuntos
DNA/química , Conformação de Ácido Nucleico , Análise de Sequência com Séries de Oligonucleotídeos/métodos , Microscopia de Fluorescência , Análise de Sequência com Séries de Oligonucleotídeos/instrumentação
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