Nanometer-sized polyhedral wire-frame objects hold a wide range of potential applications both as structural scaffolds as well as a basis for synthetic nanocontainers. The utilization of DNA as basic building blocks for such structures allows the exploitation of bottom-up self-assembly in order to achieve molecular programmability through the pairing of complementary bases. In this work, we report on a hollow but rigid tetrahedron framework of 75 nm strut length constructed with the DNA origami method. Flexible hinges at each of their four joints provide a means for structural variability of the object. Through the opening of gaps along the struts, four variants can be created as confirmed by both gel electrophoresis and direct imaging techniques. The intrinsic site addressability provided by this technique allows the unique targeted attachment of dye and/or linker molecules at any point on the structure's surface, which we prove through the superresolution fluorescence microscopy technique DNA PAINT.

1. Introduction

The design and self-assembly of DNA strands into precisely defined objects on the nanometer scale has emerged as a promising technique in the field of nanotechnology. Stemming from the initial idea of generating periodic lattices from DNA [1], the concurrent exploitation of (i) complimentary base pairing between short strands, (ii) branch-like Holliday junctions, and (iii) the inherent helical twist of double-stranded DNA complexes has allowed for the assembly of small, identical motifs which constitute the repeating unit cells of periodic two-dimensional sheets or three-dimensional crystal structures extending nearly to the millimeter scale [25]. The development of techniques to build rigid, three-dimensional DNA-based structures is, however, an important aspect to the future utilization of this methodology in nanofabrication [611]. While many attempts to construct simple three-dimensional polyhedra have been fraught with problems of instability, unwanted by-products, low-yield, or overly complex synthesis strategies, the recent utilization of hierarchical assembly schemes [12] and the DNA origami technique [13, 14] has provided a path towards the relatively simple generation of uniform populations.

The DNA origami technique is based on the use of a long, usually circular “scaffold” strand, which is folded and clamped into a desired shape by hybridization with hundreds of shorter “staple” oligonucleotides [13]. In contrast to earlier schemes for generating nanostructures from synthesized oligonucleotides, the utilization of a viral scaffold, which is typically the 7 kb circular single-stranded M13mp18 bacteriophage genome or alternatively PCR-templated products [15, 16], allows for the construction of far larger structures often extending to several hundreds of nanometers [17]. The heterogeneous sequence of the underlying scaffold strand forms the basis for the unique strength of this method, by which each staple strand has the potential to act as a “handle” for the placement of accessory molecules at virtually any site in the structure with nanometer precision [18, 19]. Through standard purification techniques, relatively uniform populations of folded structures of the desired conformation can be isolated. This method is suited not only for compact, structurally rigid objects, but also for those which incorporate single-stranded sections amongst rigidly extended helical bundles to generate objects displaying flexible hinges and inherent tensile strain [20].

Hollow, load-bearing frameworks represent one class of structures which holds a broad relevance in applied nanoscience as potential container systems. The use of programmed DNA self-assembly offers a highly suitable alternative pathway in their construction, as has been demonstrated in several recent studies. Two in particular have succeeded in generating highly uniform populations of rigid nanostructures. Small tetrahedral structures measuring less than 10 nanometers per strut have been rapidly assembled from four distinct oligonucleotides and have shown a significant mechanical stability, withstanding compression forces in excess of 100 pN before exhibiting buckling [10]. It was later demonstrated that a hierarchical self-assembly concept utilizing simple repeating motifs from a relatively small number of oligonucleotides [12] or DNA origami-based subunits [14] can be used to generate larger polyhedra suitable as containers or for the orientation of functional units in space with nanometer precision. While the above strategies based upon hybridization of shorter oligonucleotides produce high yields of correctly assembled products, the former is significantly size-limited based on its dependence on a simple annealing scheme, while the ability to selectively attach molecules at distinct points on the polyhedra constructed by hierarchical means suffers due to the redundancy of strands or units within the repeated motifs. The use of subunits constructed from DNA origami [14] can solve this issue of redundancy via a simple internal shifting of the scaffold strand; however, it does require the additional and often intricate control over correct three-dimensional orientation and self-assembly of the multiple segments. Consequently, the fabrication of enclosed hollow frames from a single DNA scaffold via the origami method, as previously demonstrated in a spherical architecture [21], offers the potential for the straightforward generation of a wide variety of fully and uniquely addressable structures.

As shown in the present study, utilization of the DNA origami method to construct a rigid, enclosed tetrahedral framework, illustrated in Figure 1, provides the ability to generate structures reaching a size of 75 nanometers along each edge while retaining the full addressability afforded by the heterogeneous sequence of the scaffold strand. Single stranded “hinges” at each of the four vertices of the tetrahedron allow for a structural variability. By selective staple oligonucleotide omission, four unique two-dimensional structures varying in length and width between 75 nanometers and 300 nanometers are generated. Even though the full three-dimensional structure displays mechanical rupture likely due to electrostatic-mediated surface binding and flow-induced shearing, proper annealing can nevertheless be confirmed through gel electrophoresis and examination of the assorted open frames. Additionally, binding of fluorescent molecules at precisely determined points on the structure emphasizes its potential to act as a three-dimensional ruler for emerging superresolution microscopy methods such as DNA-PAINT and Blink [2224].

2. Materials and Methods

2.1. Preparation of DNA Structures

Reverse-phase cartridge-purified unmodified staple oligonucleotides were shipped dry from Bioneer Corporation (Alameda, Calif, USA) and resuspended to a concentration of 100 μM in H2O. HPLC-purified dye- and biotin-modified oligonucleotides for PAINT analysis were purchased from IBA GmbH (Göttingen, Germany) at a concentration of 50 μM in H2O. The ATTO655-labeled oligonucleotide contained the sequence and the biotin-modified strand . The 8634-nucleotide-long M13mp18-phage-based scaffold strand was prepared and isolated as previously described [14].

As a general annealing condition, 10 nM of scaffold strand and 100 nM of each staple were mixed in TE buffer (10 mM Tris-HCl + 1 mM EDTA, pH 8.0 at 20°C) containing 14 mM MgCl2, heated to 80°C for 5 minutes, and quickly cooled to 60°C over 20 minutes, before being slowly cooled to 24°C in steps of 0.5°C over approximately 40 hours. When applicable for dye or biotin attachment, staple oligonucleotides with docking handle extensions replaced unextended staples in the solution and biotin- or dye-modified oligonucleotides were included at 500 nM per staple during annealing. For PAINT analysis, a total of six biotin attachment sites (two per vertex) and three ATTO655 sites (one per strut) were used to modify struts I, II, and III, as shown in Figure 4(a) and in the Supplementary Materials in Figure S1.

Gel electrophoresis was performed with an agarose concentration of either 2.0% (for band analysis) or 0.7% (for structure purification). Agarose was first heated to boiling temperature in 45 mM Tris borate + 1 mM EDTA (pH 8.2 at 20°C) then cooled to 60°C in an ice bath, at which point MgCl2 was added to a final concentration of 11 mM, before being cooled to room temperature in a gel cask. For sample preparation, 5 μL of DNA origami structures were mixed with 3 μL of 6x agarose gel loading buffer (30% glycerol weight-to-volume in water, 0.025% xylene cyanol, 0.025% bromophenol blue) and brought to a total volume of 18 μL in H2O, for roughly moles of structures per gel pocket. Similarly, bare scaffold strands were mixed with loading buffer and H2O to give a total amount of moles per sample. The different gel pockets were filled with the origami and scaffold samples along with a 1 kb DNA ladder and run for approximately 3 hours at constant 70 V over a cathode-anode distance of 22 cm. The entire apparatus was cooled in an ice water bath while running to avoid unwanted structure denaturation. Afterwards, the gel was stained with an ethidium bromide solution at 0.5 μg/mL and imaged under 302 nm UV excitation. Following electrophoresis, the primary band was excised from the gel and centrifuged at 5000 ×g for 7 minutes in spin columns (Freeze’n Squeeze Spin Columns, Biorad) to isolate structures. Purified origami samples were usually estimated to contain approximately 1 nM of annealed structures.

2.2. Visualization of Structures (TEM and AFM)

TEM Imaging
Formvar-supported carbon coated TEM grids were purchased from Plano GmbH (Wetzlar, Germany). Grids were first hydrophilicized in a Diener Electronic Femto plasma cleaner. 2 μL of purified origami samples was added to the grids, and structures were allowed to bind for 60 seconds. Excess sample was then quickly removed from the grids by absorption with filter paper. Grids were quickly washed with 1% uranyl acetate in H2O, then stained for 15 seconds with the same and allowed to dry completely. The samples were then imaged with a JEM-1011 transmission electron microscope (JEOL) operated at 100 kV.

AFM Imaging
For viewing with atomic force microscopy, 5 μL of purified origami sample placed onto a freshly cleaved mica surface (Plano GmbH, Wetzlar, Germany) which had been attached by hot glue to a 15 mm metal specimen disc (Ted Pella, Inc., Redding, Calif, USA). Structures were allowed to bind for 60 seconds before being washed twice with 30 μL of TE buffer solution containing 12.5 mM MgCl2 to remove unbound origami objects and other debris. Samples were imaged in Tapping Mode in the previously mentioned TE/Mg++ buffer conditions using a NanoScope III Multimode AFM from Digital Instruments (Veeco Instruments Ltd., Plainview, Tex, USA) with a silicon-nitride tip with a spring constant of  N/m (Veeco).

2.3. Shape Analysis by DNA PAINT

Sample Preparation
Chambered Cover Glass Slides (LabTek, NUNC, Langenselbold, Germany) were prepared for Total Internal Reflection (TIR) Microscopy in the following manner: glass surfaces were first cleaned with 0.1 M HF for 30 seconds and washed with PBS. They were then passivated with a mixture of 5 mg/mL bovine serum albumin (BSA) and 1 mg/mL biotin-conjugated BSA for 16 hours. Following a second washing with PBS to remove unbound proteins, the surface was incubated for 15 minutes with 0.01 mg/mL streptavidin (IBA GmbH) then again washed with PBS to remove any excess, unbound streptavidin. 50 μL of the sample solution which contained 90% of a 1 M MgCl2 buffer and 10% purified origami solution (for a final structure concentration of approximately 0.1 nM) was added to the chamber and allowed to bind to the surface. Binding was facilitated by biotin linkers on the origami structures, included at each vertex of the plane formed by struts I, II, and III. Chambers were again washed with PBS to remove unbound structures, and a 50 nM solution of ATTO655-labeled oligonucleotides (PAINT-DNA) in 500 mM NaCl was added.

Microscopy Setup
An inverted Olympus IX-71 in objective-type TIRF configuration outfitted with a UPlanSApo objective (100x, NA 1.40, oil immersion) was used for monitoring. Dyes were excited by a single-mode diode laser (XTL, Toptica Photonics, Grafelfing, Germany) operated at 100 mW with a wavelength of λ = 650 nm. Fluorescence was imaged on an EMCCD camera (Ixon DU-897, Andor Technologies, Belfast, Northern Ireland). Image size was 128 × 128 pixels, with each pixel representing a length of approximately 90 nm. Each acquired sequence of images contained approximately 2000 frames taken at a rate of 20 Hz.

3. Results and Discussion

3.1. Tetrahedron Design

The tetrahedral design was implemented using the caDNAno [25] software package, which was developed to facilitate the layout of both three-dimensional and flat DNA origami structures. A circular scaffold strand of 8634 nucleotides was used to allow for a maximal size, which was folded into its final configuration by a total of 211 staple strands. Each of the six struts in the tetrahedron is based on a bundle of six parallel double helices [14, 26], 227 paired bases in length, with each double helix represented by a cylinder in the three-dimensional schematic (Figure 1(a)). The bundles are connected at each of the four hinged vertices to the two neighboring bundles by a four-base single-stranded section of the circular scaffold extending between their termini, as indicated in the inset in Figure 1(b). At each vertex, adjacent double helices within a single six-helix bundle were selected as connecting points to each of the two neighboring struts so as to minimize possible strains resulting from sterically induced stretching of the roughly 4 nm single-stranded connecting section. Additionally, connection points on opposite ends of a single strut extend from the same pair of double-stranded helical sections, which minimizes any possible unfavorable twist-strain within the bundle [21, 27]. We have adopted the nomenclature as indicated in Figure 1(a) whereby each strut is labeled 1 through 6. Due to circular continuity of the scaffold strand and the periodicity of scaffold crossovers between neighboring helices within a single six-helix bundle, struts 1, 5, and 6 contain points where three scaffold crossovers are contained within a seven-base section along the double helix. As highlighted in Figure 1(c) for strut 5, the three nearly aligned gaps within the strut are stabilized only by staple oligonucleotides hybridized to scaffold sections on opposing sides of each opening. Lacking a direct connection from the internal scaffold path running throughout the structure, these junctions, referred to as 1, 5, and 6 in coordination with the previous nomenclature, must be viewed as weak points susceptible to rupture; however, they provide the overall tetrahedron with its structural variability as will be discussed in later sections. A full schematic of both scaffold and staple arrangement within the overall structure can be seen in the Supplementary Materials in Figure S1.

Specific binding of tetrahedra to surfaces was facilitated by the addition of an 18-base sequence on the 3′ end of six staples, each terminating at the end of a bundle lying on the plane formed by struts 1, 2, and 3, to which a complementary oligonucleotide containing a biotin molecule conjugated to its 3′ end could be hybridized. This allowed stable attachment of structures to surfaces coated with biotin-binding proteins such as streptavidin. The positioning of the biotin on the 3′ end of the modified strand directly abutting the structure imposes the closest possible binding between the object and surface. In a similar manner, one staple positioned along the length of each of struts 1, 2, and 3 with their 3′ terminus on the outer surface of the bundle was selected as a handle for complimentary oligonucleotides with an ATTO655 dye conjugated to the 3′ end of the strand in DNA PAINT experiments. In both cases, any combination of biotin or dye sites could be included within the structure by the replacement of normal staple strands with those extended by the complimentary “handle” or docking sequence.

3.2. Full Tetrahedron Structural Properties

The structures were annealed in a one-pot reaction in TE buffer in the presence of 14 mM MgCl2. As analyzed by agarose gel electrophoresis after annealing, well-defined bands were observed indicating a population of uniformly annealed structures, along with signs of additional slower migrating aggregate products, as can be seen in the Supplementary Materials in Figure S2. Little change in band structure was observed by varying the annealing time from 18 to 170 hours, although a lengthening of the single-stranded scaffold sections between struts caused a higher migration speed and a less-defined band structure (see Figure S2 in the Supplementary Materials). From analysis of relative band intensity in gels, the yield of primary annealed product was approximately 20%. The majority of scaffold-containing material remained in the gel pockets, where presumably aggregated structures are unable to effectively enter or migrate through the gel matrix.

Annealed objects were negatively stained with uranyl acetate and analyzed via transmission electron microscopy (TEM) for structural characteristics. Despite the defined structure of gel bands, TEM observations yielded an absence of intact tetrahedra, with a large portion of the structures displaying apparent breaks along one or more of the individual struts. Two such examples are shown in the left panel of Figure 2; the individual six-helix bundle struts appear to be well formed and connectivity within most vertices is maintained; however, the structures display a deformed or flattened configuration appearing to arise from a small number of ruptures along the length of one or two edges. Measured lengths of individual struts varied from 70 to 90 nm, close to the estimated value of 75 nm based on a 0.34 nm axial pitch between adjacent bases in the double helix.

3.3. Piecewise Verification of Proper Annealing

The pervasive existence of malformed structures under TEM observation points to one of two possible causes; either a systematic error in annealing occurs due to unexpected internal strains or kinetic traps, or properly annealed tetrahedra are denatured as a consequence of mechanical stresses endured in the process of purifying, fixing, and staining the objects. The lack of a clear predominance of any single “broken” tetrahedron configuration as viewed under TEM despite well-defined band structure in electrophoresis strongly indicates that the second consideration is the more likely explanation for the aforementioned observations. As previously emphasized, the three gap areas within each of struts 1, 5, and 6 formed by the close alignment of scaffold crossovers must be considered as weakened points along the bundles. A closer examination of the underlying staple connections across the gaps as pictured in Figure 1(c) for strut 5 shows that the hybridized sections stabilizing gaps along a single helical axis are in several cases as short as two nucleotides in overlap before the termination of the particular staple strand. While some degree of stabilization stemming from stacking interactions could occur for some abutting helices [28, 29], these points are nevertheless more susceptible to rupture under strong shear or compression forces than other points along continuous sections of a strut or at vertices. This can be understood through a simple comparison of the two different bond types responsible for stabilizing scaffolded DNA structures: hydrogen bonding of complimentary base pairing and the covalently connected polymer backbone comprising the main DNA scaffold through the structure. In the case of the former, it has been demonstrated that forces on the order of 50 piconewtons are sufficient to induce shear-oriented rupture of hybridized DNA strands [30, 31]. Conversely, earlier work has shown that covalent bonds can generally withstand forces up to the nanonewton scale before experiencing rupture [32]. Concerning the overall stability of the tetrahedron presented in this work, the relatively weak hybridized staple oligonucleotides spanning the gap regions in struts 1, 5, and 6 would be far more susceptible to rupture under external stress than any of the other areas whose stabilities are in addition to base pairing supported by the continuous, covalently-linked scaffold backbone.

Standard techniques for examining DNA-based nanostructures such as TEM or AFM depend on a strong electrostatic binding of the negatively charged structures to layers such as mica or the carbon coating on grids used for TEM, and staining protocols include washing and drying steps with rapid, high-shear addition and removal of fluids. While this has proven to cause only nominal damage to more compactly rigid structures, the weakened struts are particularly susceptible to rupture due to electrostatic-driven compression or deforming forces containing a shear component and are likely candidates for the observed open configurations compressed on the surface.

With force-induced rupturing of weakened points formed by gaps within the struts identified as a likely candidate for the observed deformation of tetrahedra, we sought to investigate the various configurations resulting from the targeted opening of those gaps in different combinations. Due to their design and the local stapling paths around these junctions, these two-dimensional conformations could be generated by the omission of staple groups spanning each of the three gaps during annealing. For this purpose, an open configuration formed by a particular combination of omitted gap staples is referred to by the number assigned to the gap or gaps presumably left open. By this nomenclature, the configuration generated by the omission of all gap staples is referred to as n156; that resulting from the opening of the gap along strut 6 is n6, and so on. While there are a total of seven possible combinations of gap staple groups which can be left out, structural redundancies mean that a total of only four possible flat configurations exist. These are roughly sketched above their corresponding lane in the gel shown in the right panel of Figure 2, with n6 being the representative structure for the three identical configurations containing a single omission.

The various flat structures were annealed and analyzed as the full tetrahedron. As can be seen in the gel in Figure 2, differences in migration and band structure amongst the variants were evident after a three-hour separation at 70 V over 22 cm in 2% agarose. Bands of the different flat two-dimensional assemblies displayed a predictably lower resolution than their fully annealed counterpart, presumably due to their increased degree of configurational flexibility around open, flexible joints. Two of these structures, the linearized n156 form and the rectangular n16, have bands with a significant population of products which migrate faster than the full tetrahedron structure containing all staples. This can be explained by the lack of structurally rigid triangular substructures within the two frames, which can lead to an elongated conformation able to effectively reptate through the gel pores. Furthermore, the geometrically redundant n15 and n56 as well as the n6 configurations all have primary populations which display a slower migration character visibly absent from the fully annealed version. In both cases, this is a strong indication that none of those are preferentially occurring in any detectible amount during annealing of the full tetrahedron and that weakened points in the struts are not ruptured within the gel. This absence of any primary product resulting from the variable open configurations which displays the same migration speed as the full tetrahedron as well as the narrow band structure of the closed tetrahedron indicate that it adopts its final, defined conformation unique from those resulting from some combination of ruptured struts. Approximate yields of primary annealed products were estimated through comparison of relative band intensities. For all opened variants, this was found to be approximately 20–25%, in a similar range as the fully annealed tetrahedron, although a lesser degree of band clarity does make any precise determination in this manner unreliable. Highest yields were found with the more flexible and elongated n156 and n16 variants, likely due to the greater amount of overall material able to enter the gel. Conversely, the most rigid of the variants containing only one gap opening (represented as n6 in Figure 2) showed the smallest yields of all products, usually under 20%; however, with the greatest clarity in band structure and highest amount of aggregation near the gel pockets.

Prominent bands of each flattened conformation were excised from the gel, and structures were isolated via spin filtration before being imaged by TEM and AFM, as shown in Figure 3. In each case, most structures were found in the configuration suggested by the pattern of openings along the struts. Vertices forming connections between three partial or complete struts appeared to be well formed, and the length of spanning segments was in the range of the ideally expected 75 nm. In some cases, partial bundles resulting from an intentionally opened gap were not clearly distinguishable, likely due to the small size of these parts and possible overlapping with other struts. Populations containing fewer deformed or aggregated objects were generally seen under observation via AFM, likely resulting from the lack of potentially harsh drying steps which are typical in uranyl acetate negative staining used for TEM observations.

Taken in concert, the different two-dimensional frames demonstrate, on an individual basis, the ability for each vertex and strut, whether continuous or containing a gap region, to correctly anneal as a part of a particular flat variant of the tetrahedron. This does not fully eliminate the possibility that unintended internal stresses resulting from closure of the full structure lead to some degree of deformation. However, the single primary band migrating with the speed different to those of all open conformations is strong evidence for the successful annealing of the full tetrahedron. From this, we can conclude that rupturing occurs during fixing and staining procedures onto carbon-coated TEM grids due to strong surface interactions from surface adsorption or transverse shear forces incurred in washing and drying steps.

3.4. Superresolution Analysis via DNA PAINT

Single-layer DNA origami structures have recently been shown to function as ideal substrates for superresolution microscopy techniques such as DNA PAINT [24] (points accumulation for imaging in nanoscale topography) or Blink microscopy [19] due to the ability to place fluorescent dyes at prescribed locations on the structure’s surface with nanometer precision. The localization of fluorescent molecules beyond the normal diffraction limit of visible light is predicated by the principle that only a single molecule within the detection area is active, that is, emitting fluorescent light, at any given time [22, 23]. Switching between ON and OFF states of fluorescent molecules is generally controlled by either chemical means or by utilizing intrinsic dark states [33]. In contrast, for systems involving interactions on surface-bound DNA-based nanostructures due to hybridization-based binding and unbinding between dye-oligonucleotide-conjugate detector strands and complimentary docking strands on the structures, switching occurs as a natural consequence of two factors: (i) freely diffusing strands within solution cause minimal background due to TIR excitement of only dyes near to the surface by the evanescent wave and (ii) a 70% increase of fluorescence is attained upon hybridization due to a significant reduction of intrastrand guanine quenching [24]. This results in the relatively straightforward detection of single hybridization events occurring between single, labeled detector oligonucleotides and complimentary docking strands extending outward from the surface of the origami object. Furthermore, control over rates of binding/unbinding events can be achieved by altering the length of the hybridized segment and concentration of the detector strand within the surrounding solution, respectively [24].

Binding of tetrahedra to a streptavidin-coated surface was accomplished by the inclusion of six handle sites for complimentary biotin-oligonucleotide hybridization, two each extending from the ends of struts 1, 2, and 3, as indicated in Figure 4(a) and in Figure S1 of the Supplementary materials. Passivation of the glass surface with a protein layer containing BSA and streptavidin has the additional advantage of shielding the negatively charged structures from the strong electrostatic binding which proves destructive to their three-dimensional morphology as seen with the carbon or mica surfaces described in the previous sections. In addition, one staple with an extended handle sequence extending from the 3′ end for ATTO655-oligonucleotide docking was incorporated into each of struts 1, 2, and 3, as outlined in detail for strut 1 in Figure 4(a) and shown for all struts in the Supplementary materials in Figure S1. The positioning of each dye site along its respective strut is shown in Figure 4(a), which together form a triangular arrangement with approximately 60 nm dimension. An 8-base docking length for the detector oligonucleotide was selected to give sufficiently long binding times for accurate position determination, and a high detector concentration of 50 nM was chosen in order to have high enough association rates [24].

Binding/unbinding events were recorded over 100 s with a capture rate of 20 Hz during TIR excitation from a single-mode diode laser with wavelength of 650 nm. Recorded movies were analyzed in a custom software package programmed in LabVIEW [34]. Spots where binding events in each frame occurred were fitted with a 2D Gaussian, and the peak coordinates of each spot were entered into a 2D histogram with a binning of 10 nm. According to the color scheme used, brighter spots represent a greater frequency of binding events at that particular position.

The left frame in Figure 4(b) shows a single snapshot of the 11.5 μm × 11.5 μm area monitored, and the two frames on the right show the superresolved 2D histograms of two different localized areas of binding/unbinding events. In contrast to raw data, the superresolved histograms of local spots indicate a localization of three peak event occurrences. The three apparent binding locations on the origami object display the correct distance scale and geometrical arrangement for spacing suggested by docking site placement along the base of the tetrahedron. Through the analysis of six docking site pairs, we found an average distance between localized histogram peaks of (68 ± 12) nm. For a comparison, the approximate expected distance of 60 nm is indicated in the image. Our data generally demonstrates the ability for DNA PAINT to resolve subdiffraction limit structures in two dimensions as well as the potential of such a DNA origami framework for superresolution techniques.

4. Conclusion

The construction of wire-frame, cage-like structures of nanometer size is an endeavor which not only holds great potential for studies requiring mechanically stable nanoscale spacers and scaffoldings but also could prove crucial for the development of containers suitable for targeted drug delivery. In this work, we have presented a DNA origami-based design for the simplest architecture of this kind; a four-faced tetrahedron consisting of six flexibly jointed struts. Analysis of annealed objects via gel electrophoresis strongly indicates the presence of a population of uniformly annealed tetrahedra comprising approximately 20% of the total number of scaffolded objects, although structures appear to suffer ruptures at select weakened points along the struts likely due to forces occurring during electrostatic adsorption to surfaces and staining procedures. Intentional, targeted opening of these weak “gaps” in the struts via selected staple oligonucleotide omission led to the formation of a set of four different open configurations, again at a yield of approximately 20%, which were analyzed by gel electrophoresis and visualized via atomic force microscopy and transmission electron microscopy. We found populations of structures that displayed the expected open morphologies when bound to surfaces, which demonstrated proper assembly of the individual vertices and full struts, further supporting the suggestion of rupture of full three-dimensional frameworks from external forces. By exploiting the nanometer-precise positioning of dyes on the tetrahedra, a key feature provided by the DNA origami technique, its triangular base was used as a stage for visualization in two dimensions with the superresolution DNA PAINT microscopy method. Analysis confirmed the triangular arrangement of attached dyes and similar spacing as predicted by the structural schematic. As a consequence, we expect such structures to be suitable test objects for 3D superresolution microscopy.

While the observed breakage of the tetrahedra at weakened points along the struts is proposed to arise from external stresses during fixation and staining, this apparent structural instability under stress is nevertheless a concern for future implementation of such objects as stable load-bearing scaffolds or cargo-bearing containers. This can potentially be resolved by longer overlaps between the connecting staples spanning the individual helices or by the incorporation of a linear scaffold strand into future designs to reduce the weakened gap regions along the struts imposed by the necessity of maintaining circular scaffold continuity. Enzymatic ligation of abutting 3′ and 5′ ends of staples within origami structures has been posited as a potential means to increase the overall stability of single-layer architectures [35] and could serve to further strengthen three-dimensional frameworks as presented in this work. Additionally, recently developed techniques for metallization of DNA nanostructures could be applied as a potential means to mechanically stabilize and electrically functionalize the tetrahedron and its two-dimensional variants [3638].


This work was financially supported by funding from NIM, CeNS, and DFG (LI1743/2-1, TI329/5-1). The authors would like to additionally acknowledge Dr. Susanne Kempter for assistance with transmission electron microscopy imaging and both Philipp Nickels and Dr. Ralf Jungmann for their help with atomic force microscopy visualization.

Supplementary Materials

Additional supplementary materials contain a diagrammatic design layout of the structure, agarose gel analysis of folding conditions and sequences of all oligonucleotides utilized in this study.

  1. Supplementary Materials