DNA-Scaffolded Proximity Assembly and Confinement of Multienzyme Reactions

Abstract

Cellular functions rely on a series of organized and regulated multienzyme cascade reactions. The catalytic efficiencies of these cascades depend on the precise spatial organization of the constituent enzymes, which is optimized to facilitate substrate transport and regulate activities. Mimicry of this organization in a non-living, artificial system would be very useful in a broad range of applications—with impacts on both the scientific community and society at large. Self-assembled DNA nanostructures are promising applications to organize biomolecular components into prescribed, multidimensional patterns. In this review, we focus on recent progress in the field of DNA-scaffolded assembly and confinement of multienzyme reactions. DNA self-assembly is exploited to build spatially organized multienzyme cascades with control over their relative distance, substrate diffusion paths, compartmentalization and activity actuation. The combination of addressable DNA assembly and multienzyme cascades can deliver breakthroughs toward the engineering of novel synthetic and biomimetic reactors.

Introduction

Multistep enzyme pathways play critical roles in cellular metabolism that produces biomolecules and harvests energy for sustaining and propagating living systems. As of 2019, 7727 different enzymes have been recorded in the BRENDA database, a comprehensive enzyme information system, including enzymes found in human cells and bacteria. These enzymes catalyze more than 5000 different biochemical reactions in the human body [1]. Enzyme cascades are highly sophisticated systems that control and regulate thousands of chemical reactions in cells. Peter Roach described chaos reactions with a set of spatio-temporally disorganized enzymes as a symphony without a conductor [2] (Fig. 1a). Enzyme cascades, therefore, can behave as a conductor of a symphony, controlling and guiding biochemical reactions into productive and coordinated pathways. The functions of many pathways critically depend on the relative position, orientation and number of participating enzymes [3, 4]. Living things have evolved several strategies to organize and confine multienzyme reactions. One such strategy is a protein scaffold, such as the long, glycoprotein “scaffold” used by cellulosomes to selectively integrate various cellulases and xylanases into a proximity complex for the efficient binding and degradation of cellulose [5] (Fig. 1b). Another example is substrate channeling; as shown in Fig. 1c, an indole tunnel observed in a tryptophan synthase α₂β₂ complex passes indole intermediates between active sites of the alpha subunit and beta subunit at a very rapid rate of 1000 s⁻¹ or faster [6]. A third biological strategy, compartmentalization, shown in Fig. 1d, is used by bacterial carboxysomes to carry out carbon dioxide (CO₂) fixation [7].

Fig. 1.

Cellular multienzyme cascade pathways. a A cartoon of symphony performance to describe the integrated and regulatory function of enzyme cascades. Reproduced from Roach [2], with permission, copyright 1977, Trends in Biochemical Sciences. b The proximity assembly of enzymes on a protein scaffold in a cellulosome. Reproduced from Bayor et al. [5], with permission, copyright 2004, Annual Review of Microbiology. c Substrate channeling in tryptophan synthase. Reproduced from Miles et al. [6], with permission, copyright 1999, American Society for Biochemistry and Molecular Biology. d Confined carbon dioxide (CO₂) fixation in a carboxysome. Reproduced from Yeates et al. [7], with permission, copyright 2010, Annual Review of Biophysics

The ability to exert control over these biochemical pathways on the nanoscale will not only increase our understanding of cellular metabolism, but also provide innovative tools to mimic and translate cellular mechanisms into non-living artificial systems for novel applications. Recent decades have seen the development of various approaches to create artificial multienzyme complexes, including genetic fusion [8], chemical crosslinking [9], surface co-immobilization [10], polymer vesicles [11–13] and virus-like particles [14, 15]. However, several obstacles remain in terms of their broader applications, such as limited control over the spatial arrangement (sizes and shapes), low encapsulation yield of large proteins due to steric hindrance, insufficient access of substrates to enzyme assemblies and aggregation of vesicle shells. It also remains challenging to engineer biomimetic functions on nanoreactors, such as artificial nanopores that govern the transmembrane diffusion of molecules and the feedback regulation of enzyme functions.

Double-stranded DNA (dsDNA) is a self-assembling biopolymer that is directed by Watson–Crick base pairing. Ned Seeman first proposed and demonstrated that artificially branched DNA tiles could be assembled by rationally designed single-stranded DNA (ssDNA) [16]. Such structures can have complex shapes beyond those attained by biological evolution and can be designed using “simple” elements, such as the “Holliday” junction (Fig. 2a) and double-crossover (DX) tiles (Fig. 2b) [16–19]. Two key breakthroughs in structural DNA nanotechnology are scaffolded DNA origami, invented by Paul Rothemund in 2006 (Fig. 2b) [20], and ssDNA tiles (SST), reported by Peng Yin in 2012 (Fig. 2c) [21, 22]. These methods have empowered the design and fabrication of complex and multidimensional nanostructures, including one-dimensional (1D) nanotubes, two-dimensional (2D) rectangular or triangular shapes [20], curved containers [23, 24], nanoscale polyhedrons [25], polyhedral meshes [26, 27] and periodic DNA crystals [28, 29]. Recent progress has been made to scale up DNA assemblies in terms of size and quantity [30] and to fold nanostructures with single-stranded nucleic acids [31]. To facilitate the design of DNA nanostructures, several computational tools, including TIAMAT [32], NUPACK [33], caDNAno [34] and CanDo [35], have been developed that benefit researchers worldwidely.

Fig. 2.

Overview of structural DNA nanotechnology. a A four-way “Holliday” junction. Reproduced from Seeman [19], with permission, copyright 2003, Springer Nature. b DNA double-crossover (left) and triple-crossover (right) tiles. Reproduced from Zadegan and Norton [18], with permission, copyright 2012, MDPI. c DNA origami assembly. Reproduced from Rothemund [20], with permission, copyright 2006, Springer Nature. d Assembly of single-stranded DNA tiles. Reproduced from Wei et al. [21], with permission, copyright 2012, Springer Nature. e DNA scaffold-directed assembly of biomolecular complexes. Reproduced from Fu et al. [36], with permission, copyright 2019, John Wiley and Sons

DNA nanostructures are promising assembly scaffolds for positioning other elements into diverse patterns at the nanoscale [36, 37]. As shown in Fig. 2d, DNA scaffold-directed assembly has the advantages of programmable and prescribed geometry, sequence-addressable assembly and adaptability to various bioconjugations [36]. Utilizing these unique features, Researchers have used DNA nanostructures to assemble complex biomolecular systems, such as multienzyme complexes, protein confinement and biomimetic channeling [37, 38]. They have also been used to guide the assembly of synthetic vesicles, including membrane confinement [39, 40] and transmembrane nanopores [41, 42].

In this review, we summarize and discuss the recent progress in the field of DNA scaffold-directed assembly of multienzyme reactions, including proximity assembly, confinement, biomimetic substrate channeling and regulation circuits, as well as bioconjugation techniques of hybrid DNA–protein structures.

Protein–DNA Bioconjugation

A variety of chemical methods have been developed to attach proteins to DNA nanostructures [37, 43]. Most DNA–protein conjugations can fall into one of three categories: covalent crosslinking, noncovalent binding and fusion tags (summarized in Table 1). Covalent crosslinking usually involves conjugation of an existing amino acid group (e.g. primary amine or thiol) on the protein surface to a chemically modified oligonucleotide. For example, succinimidyl-4-(N-maleimidomethyl) cyclohexane-1-carboxylate (SMCC) and succinimidyl 3-(2-pyridyldithio) propionate (SPDP) are two widely used crosslinkers that conjugate a primary amine from a lysine residue on an enzyme surface to a thiol-modified oligonucleotide [44, 45]. The difference between the two crosslinkers is that the disulfide linkage of SPDP is cleavable upon the addition of a reducing reagent, such as T-CEP or mercaptoethanol, while the linkage of SMCC is not cleavable. SMCC and SPDP crosslinkers are generally not site-specific in their reaction with lysines due to the presence of multiple lysine residues on the protein surface. The product of such non-specific conjugation is a heterogeneous mixture of DNA-tagged proteins. In some studies, SMCC or SPDP was used to conjugate a cysteine residue of a protein with an amine-modified DNA strand. This could be site-specific if there were only one cysteine displayed on the protein surface, such as cytochrome c [46]. Another commonly used crosslinker is disuccinimidyl suberate (DSS) in which the double succinimide ends can react with two primary amines to link them together [47]. DSS is especially useful for conjugating amine-modified ssDNA with organic cofactors, such as NAD or ATP [47–49].

Table 1.

Summary of protein–DNA conjugation chemistry

Chemistry	Reagenta	Reactive groups	Site-specific
Covalent crosslinking	SMCC [44]	Primary amine and thiol	No
	SPDP [45]	Primary amine and thiol (cleavable)	No
	DSS [38]	Amine	No
	Click chemistry [50]	Alkene and azide	Depends on labeling position
	N-terminus conjugation [52]	Pyridoxal phosphate (PLP)-mediated transamination	N-terminus amino acid
	DNA-templated protein conjugation [55]	Primary amine on lysine	Approximate position

Chemistry	Ligand	Binding affinity	Site-specific
Noncovalent binding	Biotin–streptavidin [58]	Kd~ 10−12–10−15 M	Depends on labeling position
	Aptamer–protein [62]	nM to µM Kd	Yes
	Cofactor–apozyme [66]	pM to µM Kd	Yes

Chemistry	Tag/fusion	Ligand	Site-specific
Peptide tag/protein fusion	His-Tag [67]	Ni-NTA	N- or C-terminus
	Intein [68]	N-terminal cysteine	N-terminus
	DegP [72]	DPMFKLV	N-terminus
	Halo [69]	Chlorohexane (CH)	Preferred C-terminus
	SNAP [69]	Benzylguanine (BG)	N- or C-terminus
	MTG [70]	Carbobenzyloxy glutaminyl glycine (Z-QG)	N-terminus
	CLIP [54]	Benzylcytosine (BC)	N- or C-terminus
	HUH [71]	Endonuclease	N- or C-terminus
	DNA-binding protein	TAL effector [73]	N- or C-terminus

K_d, Dissociation constant

^aSee Abbreviation list

Considerable progress has been made over the past two decades to improve the site-specificity of DNA–protein crosslinking. Click reactions (such as copper-catalyzed, azide-alkyne cycloaddition) combined with non-natural amino acid incorporation can produce easily purified conjugates with high site-specificity and yield [50]. To reduce the toxic damage of copper ions, Khatwani et al. used a copper-free click reaction (e.g. strain-promoted [3 + 2] azide-alkyne cycloaddition) to produce protein–DNA conjugates [51]. Francis and coworkers reported a protein bioconjugation at an N-terminal amino acid via a pyridoxal 5′-phosphate (PLP)-mediated transamination reaction [52], and Takeda et al. reported the development of a method to chemically modify an oligonucleotide to a N-terminal cysteine of a protein [53]. Proximity ligation has also been applied to site-specific labeling of an oligonucleotide on a protein by affinity binding-mediated conjugation [54]. Rosen et al. developed a DNA-templated protein conjugation (DTPC) technique to create site-selective DNA–protein conjugation [55]. In the DTPC technique, a guiding DNA strand first co-locates with a metal-binding site of a protein, followed by the introduction of a second DNA strand that conjugates to the lysine residues in the vicinity of the metal-binding site. For a more detailed discussion of site-selective conjugation of native proteins with DNA, the reader is referred to a recent review by Trads et al. [56].

Noncovalent binding may also be used to link DNA with proteins. The classic example is that of the strong binding of biotin to streptavidin [dissociation constant (K_d) < 10⁻¹² M] to attach a biotinylated DNA to a streptavidin [57] or streptavidin-tagged enzymes [58]. With the development of oligonucleotide aptamers, aptamer-directed assembly has been adapted to immobilize proteins onto DNA nanostructures by site-specifically incorporating aptamer sequences into DNA nanostructures. This approach has been demonstrated to effectively anchor multiple protein targets onto rationally-designed DNA nanoscaffolds, including thrombin [59], platelet-derived growth factor [60] and cell–cell interactions [61]. More importantly, DNA nanostructures can be used to organize multivalent aptamers with optimized spacing distances to enhance their binding affinity [62]. These spatially optimized multivalent aptamers bind to a protein with low nanomolar—or even picomolar—K_d, whereas a single aptamer–protein binding is much weaker with several hundred-fold higher K_d [62, 63]. Similarly, short polypeptide ligands can also be positioned onto the surface of DNA nanostructures for protein binding (e.g. antibody, tumor necrosis factor-α and transferrin) [64, 65]. In addition to aptamers, reconstituted apoenzymes are used to tightly bind to an organic cofactor-modified oligonucleotide [66].

Genetically modified proteins with a short peptide tag or a fusion tag offer more control over the site-specificity of any DNA–protein conjugation. Poly(histidine)₆ is one widely used peptide tag that can be incorporated into either the N- or C-terminus of a protein by binding to a nitrilotriacetic acid (NTA)-modified oligonucleotide in the presence of nickel ions [67]. In the last 20 years many techniques have been developed for constructing recombinant (terminus fused) proteins that can bind with ligand-modified nucleic acids. For example, intein-fused proteins can ligate with an N-terminal cysteine-tagged oligonucleotide via the formation of a peptide bond linkage [68]. The research group of Niemeyer and coworkers used “Halo-tag”- and “SNAP-tag”-modified proteins to conjugate with chlorohexane (CH) or benzylguanine (BG)-modified oligonucleotides, respectively [69]. Similar examples of fusion-mediated DNA–protein conjugation include a microbial transglutaminase (MTG) fusion [70], a CLIP tagging [54], a HUH tagging [71] and a DegP (serine protease) fusion [72]. Additionally, Dietz and coworkers recently used transcription activator–like (TAL) effector proteins to recognize and bind to specific DNA sequences for creating DNA–protein hybrid nanostructures [73]. These TAL effectors can be genetically introduced into the sequence of other enzymes for anchoring them onto DNA nanostructures.

Following conjugation, the purification of DNA-conjugated proteins is especially important to produce a high-quality sample. The presence of unconjugated DNA or free proteins decreases the assembly yield of proteins onto DNA nanostructures. The most common purification methods include molecular-weight cutoff filtration, gel electrophoresis and chromatography. Due to the negative charge of the DNA phosphate backbone, ion-exchange chromatography is the preferred method to purify DNA-conjugated proteins while separating proteins labeled with different numbers of DNA sidechains. Detailed procedures for purifying DNA-conjugated proteins have been summarized in a recently published protocol [38].

Spatial Organization of Multienzyme Assemblies on DNA Nanostructures

In cellular metabolism, the function of multienzyme cascades largely depends on their spatial organization, such as the relative distance, orientation, stoichiometry and confinements of the individual protein components [3]. Self-assembled DNA nanostructures are promising scaffolds on which to organize macromolecules because of the spatial addressability of DNA nanostructures [36]. Through various conjugations linking proteins with nucleic acids, DNA nanostructures are capable of controlling multienzyme assemblies in 1D, 2D, and three-dimensional (3D) geometric patterns that can be used to boost catalytic efficiency, improve reaction selectivity and investigate mechanistic kinetics of multienzyme reactions.

Early efforts in this field started with CM Niemeyer’s work of aligning enzymes on linear dsDNA scaffolds [58]. As shown in Fig. 3a, a bienzymatic NAD(P)H:FMN oxidoreductase (flavin reductase) and luciferase cascade were assembled together onto a dsDNA scaffold via the strong binding of biotinylated enzymes with DNA-streptavidins [58]. A similar strategy was later used to assemble a cytochrome P450 BM3 enzyme on an adjustable dsDNA scaffold that could vary the distance between the two chimeras of the BMR reductase domain and the BMP porphyrin domain (Fig. 3b) [74]. Linear dsDNA scaffolds have also been used to guide the assembly of artificial cellulosomes composed of multiple cellulases [75–78]. As shown in Fig. 3c, the research group of Chen and coworkers used zinc-finger protein (ZFP) fusion to guide the assembly of two ZFP-appended proteins (an endoglucanase CelA and a cellulose-binding module CBM) into a bifunctional cellulosome structure for enhanced cellulose hydrolysis [76]. Rolling circle amplification (RCA) can produce long ssDNA scaffolds using a circular vector, a primer and a polymerase [77, 79]. As shown in Fig. 3d, these long ssDNA scaffolds produced by RCA can be used to anchor multiple copies of enzyme cascades via specific hybridizations between the section of DNA templates and the anchor DNA on the enzymes [77].

Fig. 3.

Assembly of enzyme cascades on linear double-stranded DNA scaffolds. a NAD(P)H:FMN oxidoreductase and luciferase cascade. Reproduced from Niemeyer et al. [58], with permission, copyright 2002, John Wiley and Sons. b Engineered cytochrome P450 BM3 complex varying the distance between the BMR reductase domain and the BMP porphyrin domain. Reproduced from Erkelenz et al. [74], with permission, copyright 2011, American Chemical Society. c Zinc finger protein (ZFP)-appended proteins for cellulose degradation. Reproduced from Sun et al. [76], with permission, copyright 2013, Royal Society of Chemistry. d Rolling circle amplification (RCA) assembly of multienzyme nanowires to promote cellulose degradation. Reproduced from Sun and Chen [77], with permission, copyright 2016, Royal Society of Chemistry

2D and 3D DNA nanostructures offer the ability to design more complex geometric patterns of multienzyme systems. As shown in Fig. 4a, the Wilner research group reported the self-assembly of a two-enzyme cascade array on 2D hexagonal DNA tiles with a controlled distance between enzymes [44]. The assembled glucose oxidase (GOx)–horseradish peroxidase (HRP) cascade showed a more than tenfold activity enhancement compared with unassembled enzymes. To precisely control the spacing distance between enzymes, Fu et al. organized a GOx–HRP pair on a rectangular DNA nanostructure with controlled distances between enzymes that varied from 10 to 65 nm (Fig. 4b). This spatially organized assembly was used to probe the distance-dependent activity of enzyme cascade reactions and to enhance the mass transport of the H₂O₂ intermediate [45]. Similarly, Morii and coworkers reported the assembly of an NAD⁺ cofactor-coupled enzyme cascade of xylose reductase and xylitol dehydrogenase on a 2D DNA origami for carrying out the conversion of xylose into xylulose (Fig. 4c) [81]. The close proximity of two enzymes was found to facilitate the recycling of NAD⁺ to NADH, thereby increasing the xylulose production rate. A subsequent study by the same group extended the assembly of a three-enzyme cascade converting xylose to xylulose 5-phosphate with coupled NAD⁺ and ATP cofactors [82]. As shown in Fig. 4d, the research group of Yan and coworkers demonstrated a three-enzyme pathway involving malic dehydrogenase, oxaloacetate decarboxylase and lactate dehydrogenase on a triangular DNA origami [83]. The geometric patterns of these assembled enzyme complexes were found to affect the overall pathway activities by promoting the recycling rate of cofactors in the coupled reactions. Regarding 3D structures, the Fan research group developed a one-pot assembly of DNA nanostructures by rolling a rectangular DNA origami into a DNA nanotube (Fig. 4e) [80]. Using this strategy, enzyme cascade pairs were first anchored onto a rectangular origami, followed by structural rolling to confine enzymes to the exterior of a DNA nanotube, enhancing the cascade’s activity.

Fig. 4.

Enzyme cascades organized on two-dimensional DNA nanostructures. a A glucose oxidase–horseradish peroxidase (GOx/HRP) cascade array on two-dimensional (2D) hexagonal DNA strips. Reproduced from Wilner et al. [44], with permission, copyright 2009, Springer Nature. b Organization of a GOx/HRP cascade on DNA origami tiles with controlled spacing. Reproduced from Fu et al. [45], with permission, copyright 2012, American Chemical Society. c Assembly of an NAD cofactor-coupled enzyme cascade (XR xylose reductase, XDH xylitol dehydrogenase). Reproduced from Ngo et al. [81], with permission, copyright 2016, American Chemical Society. d A three-enzyme (MDH malic dehydrogenase, OAD oxaloacetate decarboxylase, LDH lactate dehydrogenase) cascade organized on a triangular DNA origami structure. Reproduced from Liu et al. [83], with permission, copyright 2016, John Wiley and Sons. e A rectangular DNA origami rolling into a DNA nanotube for assembly of an enzyme cascade. Reproduced from Fu et al. [80], with permission, copyright 2013, American Chemical Society

In addition to DNA, RNA molecules can also be engineered into discrete and multidimensional nanostructures [31, 84]. Because RNA structures can be expressed inside cells, they offer the capability to organize metabolic pathways for in vivo applications. Delebecque et al. designed and assembled multiple shapes of discrete 1D and 2D RNA nanostructures that were formed inside cells (Fig. 5a) [85]. Using these RNA assemblies, they demonstrated an organized [FeFe]-hydrogenase and ferredoxin reaction network which enhanced the biological hydrogen production up to 48-fold. A continuous study from the research group of Silver and coworkers showed that RNA scaffolds could be used to co-localize proteins and to increase the metabolic output of a two-enzyme pentadecane production pathway in Escherichia coli (Fig. 5b) [86]. Nevertheless, potential applications of RNA scaffolds face challenges in terms of in vivo stability, survival of engineered cells, and loss of RNA information during cell division.

Fig. 5.

In vivo assembly of enzyme cascades on RNA nanostructures. a Organization of [FeFe]-hydrogenase and ferredoxin on one-dimensional (1D) and 2D RNA nanostructures (top) with enhanced hydrogen production in vivo (bottom). Reproduced from Delebecque et al. [85], with permission, copyright 2011, The American Association for the Advancement of Science. b Assembly of a two-enzyme pentadecane production pathway on RNA scaffolds (top) with enhanced pentadecane output in vivo (bottom). Reproduced from Sachdeva et al. [86], with permission, copyright 2014, Oxford University Press

DNA nanostructure-organized systems offer an opportunity for investigating the detailed kinetics of enzyme cascade reactions. One conception of the past several decades is that the proximity of enzymes promotes the mass transport of intermediate substrates between enzymes, which in turn boosts the overall activity of enzyme cascade reactions [6, 87, 88]. This theory/hypothesis seems to be supported by some recent studies of assembled enzyme cascades on DNA scaffolds [44, 45, 80, 81, 85] and metabolon engineering [8, 89], in which multienzyme complexes reacted with proximity assembly more actively than did unassembled and freely diffused enzymes. However, this hypothesis is problematic if we consider the fact that many small-molecule substrates diffuse quite quickly in solution, with diffusion coefficients ranging from 100 to 1000 µm²/s. To interpret the diffusion, Fu et al. described the concentration profile of a H₂O₂ intermediate in a coupled GOx–HRP reaction by Brownian motion (Fig. 6a), which was simulated based on Eq. (1): [45]

$$n(r,t)=\sum _{i=0}^{i=\frac{t}{\tau }-1}\frac{1}{{\left(4\pi D\left(t-i\times \tau \right)\right)}^{\frac{3}{2}}}\times exp\left(-\frac{r^2}{4D\left(t-i\times \tau \right)}\right),$$ 1

where n(r, t) is the number of molecules at a distance r from the initial produced position of production, D is the diffusion coefficient and t is the time given for diffusion. When the Brownian motion of H₂O₂ is considered in a GOx–HRP reaction in the given t, τ is the average time between GOx turnovers (τ  = 1/k, where k is the turnover rate). The simulation of the diffusion profile showed that H₂O₂ concentrations varied slightly (< 5%) within a few hundred nanometers of GOx due to the fast diffusion of H₂O₂ (D  ~ 1000 µm²/s). This simulation result suggests that the proximity between enzymes has little benefits on the diffusion of H₂O₂ from GOx to HRP. As shown in Fig. 6b, Wheeldon et al. applied Eq. (1) to simulating the concentrations of product molecules at discrete distances from the active site of an enzyme as a function of k/D [90]. For most enzymes, the diffusion coefficients (generally ~ 100 to 1000 µm²/s) of the small-molecule products were much larger than the turnover rates (generally ~ 1–100 s⁻¹), resulting in a small value of k/D (0 <  k/D < 1). Thus, product concentration profiles are spanned quite uniformly over a few micrometers distance, a result which also indicates the minimal effect of spatial proximity on the concentration of intermediates in a cascade reaction. Hess and coworkers mathematically modeled the reaction–diffusion kinetics of a GOx–HRP cascade reaction [91, 92]. The simulation of cascade kinetics showed that proximity did not contribute to the activity enhancement of the assembled GOx–HRP pairs. Other more recent reaction–diffusion modelings suggested that a close proximity between enzymes could only enhance the rate of a cascade reaction under crowding conditions where the diffusion of enzymes and substrates was significantly slowed down [93]. Similar modeling techniques have also been applied to in vivo metabolic pathways, which likewise showed that diffusion was not a rate-limiting factor for many enzyme systems and, therefore, proximity or substrate channeling would not significantly increase the overall rate of the cascade reaction at steady state [88, 93]. Thus, substrate channeling is more likely used to regulate metabolite flux, improve pathway selectivity and protect metabolites from degradation or competing side reactions [88, 93].

Fig. 6.

Theoretical modeling of distance-dependent enzyme cascade reactions. a Brownian diffusion of H₂O₂ in a GOx/HRP reaction depending on distance [n(r, t) Number of molecules at a distance r from the initial produced position of production]. Reproduced from Fu et al. [45], with permission, copyright 2012, American Chemical Society. b Concentration profiles of the reaction product as a function of radial distance (r) from an active site under different ratios of turnover frequency to diffusion coefficient (k/D). Reproduced from Wheeldon et al. [90], with permission, copyright 2016, Springer Nature

Since proximity-enhanced mass-transport effect may not contribute to the activity enhancement of enzyme assemblies directed by DNA/RNA scaffolds or protein scaffolds, some recent studies have focused on the effects of assembly scaffolds themselves on altering enzyme kinetics, with the aim to provide unique microenvironments that favor stronger activity [88, 94, 95]. Such effects include modifying the local pH [96], including a hydration layer [94] and exerting an inhibitory effect [97]. Scaffolded microenvironments will be discussed in more detail in next section Enzyme Compartmentalization by DNA Nanocages. For non-freely diffused systems (e.g. constrained diffusion on a surface or within a compartment), the appropriate organization of multienzyme systems is still essential to maximize the efficiency of the system [47]. Some recent modeling studies have provided novel perspectives on enzyme assemblies on surfaces [98, 99] or within compartments [100, 101].

Enzyme Compartmentalization by DNA Nanocages

Many metabolic pathways are organized by confinement within membrane-delimited or membrane-free compartments, such as mitochondria, lysosomes, peroxisomes, carboxysomes and metabolosomes [102]. Compartmentalization affects biochemical reactions in many ways: by increasing local concentrations, facilitating mass transport of reaction intermediates, reducing toxicity of intermediates and protecting encapsulated contents from competing pathways [103]. Compartmentalization also plays a functional role in the chaperone-assisted folding of tertiary and quaternary protein structures and by preventing proteins from aggregating under cellular stress conditions [104]. Results from recent studies show that nucleoli could promote structure maintenance of nuclear proteins by compartmentalization in the presence of stressors [105].

The assembly of a DNA nanocube was first reported by the research group of Seeman and coworkers in 1991 (Fig. 7a) [106]. However, the constructed cage was not tested for the encapsulation of proteins or other large biomolecules. In 2006, Turberfield and coworkers designed a DNA tetrahedron with each edge comprising a 20-bp double helix (~ 7 nm) (Fig. 7b) [107]. This tetrahedron was shown to encapsulate a small protein [cytochrome c (inner diameter ~ 3.5 nm)]. The research group of Fan and coworkers very recently reported that the electroactivity of cytochrome c is enhanced on tetrahedral DNA frameworks [108]. As shown in Fig. 7c, DNA polyhedra have been used to organize streptavidin proteins into various 3D patterns [109]. To encapsulate larger proteins, DNA origami nanocages have been designed with larger inner cavities that range from 10 to 50 nm [110]. Zhao et al. developed a general approach to encapsulate enzymes within a fully closed DNA nanocage (Fig. 7d) [94]. In their method, enzymes are first anchored onto open, half cages at a very high yield (> 90%), following which two half cages are combined into a closed cage by adding bridge strands [94]. Sprengel et al. reported the selective encapsulation of a protein guest into a DNA origami hollow cage by decorating multiple ligands on the inner surface of the cage to guide supramolecular interactions (Fig. 7e) [72]. This noncovalent protein–ligand binding enabled the capture of very large protein complexes (up to DegP₂₄, ~ 1 million Da) into a well-defined DNA host.

Fig. 7.

Development of DNA nanocages for enzyme encapsulation. a The first 3D DNA cube. Reproduced from Seeman [19], with permission, copyright 2003, Springer Nature. b A DNA tetrahedron for encapsulating a protein. Reproduced from Erben et al. [107], with permission, copyright 2006, John Wiley and Sons. c DNA polyhedrons for organizing proteins (STV streptavidin). Reproduced from Zhang et al. [109], with permission, copyright 2019, John Wiley and Sons. d The combination of half DNA nanocages for enclosing enzymes. Reproduced from Zhao et al. [94], with permission, copyright 2016, Springer Nature. e Protein encapsulation into a DNA host using noncovalent protein–ligand interactions. Reproduced from Sprengel et al. [72] under the terms and conditions of the Creative Commons Attribution 4.0 International License, copyright 2017, Springer Nature

Regarding smart nanoreactors, switchable DNA nanocages have been designed to regulate the encapsulation and release of protein payloads. As shown in Fig. 8a, Fan and coworkers developed a single-step wrap-over of a planar DNA origami sheet into nanoribbons and nanotubes which they used to encapsulate enzyme cascades [80]. The research group of Knudsen and coworkers designed a temperature-sensitive DNA nanocage which exhibited a closed conformation at 4 °C and an open conformation at 37 °C (Fig. 8b) [111]. This switchable nanocage was used to encapsulate and release HRP in response to temperature. Kohman et al. reported a light-triggered release of bioactive cargoes of proteins and small molecules from a DNA nanocage through the incorporation of a photolabile crosslinker (Fig. 8c) [112]. An o-nitrobenzyl motif was photocleavable upon ultraviolet (UV) radiation at 240–400 nm to release a linked cargo of protein or small molecules. Kim et al. designed a pH-switchable DNA tetrahedron for regulating protein stability against protease digestion, protein–antibody binding and enzyme activity (Fig. 8d) [113]. Andersen and coworkers designed a DNA nanovault to control the access of substrate molecules to encapsulated enzymes by the reversible opening (accessible to substrate) and closing (inaccessible) of the cage (Fig. 8e) [114].

Fig. 8.

DNA nanocage-regulated encapsulation and release of protein cargoes. a Single-step folding of DNA nanotubes for enzyme encapsulation. Reproduced from Fu et al. [80], with permission, copyright 2013, American Chemical Society. b A temperature-sensitive DNA nanocage for encapsulating and releasing an enzyme. Reproduced from Juul et al. [111], with permission, copyright 2013, American Chemical Society. c A light-triggered release of bioactive cargoes from a DNA nanocage. Reproduced from Kohman et al. [112], with permission, copyright 2016, American Chemical Society. d A pH-switchable DNA tetrahedron for regulating protein stability and activity. Reproduced from Kim et al. [113], with permission, copyright 2017, American Chemical Society. e A DNA nanovault with reversible opening and closing to regulate enzyme–substrate accessibility. Reproduced from Grossi et al. [114] under the terms and conditions of the Creative Commons Attribution 4.0 International License, copyright 2017, Springer Nature

More interestingly, DNA nanoscaffolds have been found to affect the activities of the enzymes that were attached onto them. Figure 9 summarizes some of the DNA structures that have been reported to enhance enzyme activities [115], including a long dsDNA molecule (e.g. λDNA, ~ 1–2 fold improved activity) [116], a DNA structure binding to enzyme substrates (~ 1–2 fold) [117], a 2D rectangular DNA origami (~ 1–3 fold) [45], DNA nanocaged enzymes (~ 3–6 fold) [94, 118] and DNA-crowded enzyme particles (~ 2–3 fold) [95]. To better understand these effects, several mechanisms have been proposed to interpret DNA scaffolds-enhanced enzyme activities, including locally decreased pH on the DNA scaffolds [115], the presence of a stabilized hydration layer by DNA phosphate backbones [94], nanoconfinement of water [119], enrichment of substrate molecules on DNA scaffolds [117] and substrate channeling [45, 47]. However, many questions still remain on just how DNA confinements modify the local chemical and physical environment and affect enzyme functions. Experiments combining experimental data with molecular modeling may shed light on the chaperone-like function of DNA nanocages.

Fig. 9.

Enhancement of enzyme activity by DNA nanostructures. Reproduced from Zhang and Hess [115], with permission, copyright 2017, American Chemical Society

Biomimetic Assembly of Macromolecular Complexes

Biomimetic systems represent one of the most exciting research frontiers in the twenty-first century. Life on earth has been diversifying for nearly four billion years, evolving into complex and diverse species. All living organisms have developed the appropriate functions and solutions to address the challenges of Earth’s environment. Living systems have inspired humanity and provided the principles to solve problems and explore questions both in and out of the laboratory. Biomimetic materials have shown exciting potential in applications ranging from catalysis and energy transformation to smart materials, diagnostic tools and therapeutics [120]. Equally, structural DNA nanotechnology has been applied to engineering artificial systems mimicking cellular structures and biological functions. In the following paragraphs we list several examples of DNA-scaffolded biomimetic assemblies.

The swinging arm, or the covalently attached prosthetic group, is a key functional structure in substrate channeling in multistep catalytic transformations within metabolic pathways [121]. For example, a lipoyl-lysine arm is found in the pyruvate dehydrogenase complex (Fig. 10a); this arm transfers acetyl CoA and carries out oxidation and reduction between three enzymes [122]. To mimic this, Fu et al. designed an NAD⁺-modified DNA arm that facilitated the hydride transfer between two dehydrogenases [47]. As shown in Fig. 10b, a two-enzyme cascade consisting of a glucose-6-phosphate dehydrogenase (G6PDH) and a malate dehydrogenase (MDH) was displayed on a DX tile. An NAD⁺-modified poly(T)₂₀ was placed halfway between G6PDH and MDH. The activity of the cascade was enhanced by approximately 90-fold by substrate channeling of one NAD⁺ arm (Fig. 10c). Adjusting the number of swinging arms produced even more activity enhancement. As shown in Fig. 10d, the reaction specificity of the G6PDH–MDH cascade was also increased in the presence of a competing enzyme of lactate dehydrogenase (LDH). NAD⁺-modified DNA arms have also been successfully used to regulate the pathway direction between G6PDH–MDH and G6PDH–LDH [123], with the directional regulation of enzyme pathways controlled by DNA strand displacement [123] or the photo-responsive reaction (Fig. 11a) [124]. Additionally, swinging arms have been used to organize NAD⁺ transfer in a 2D enzyme array of G6PDH and LDH (Fig. 11b) [125].

Fig. 10.

Biomimetic assembly of swinging arms. a Swinging domains in pyruvate dehydrogenase complex. Reproduced from Perham [121], with permission, copyright 2000, Annual Review of Biochemistry. b An artificial swinging arm to transfer NAD⁺ cofactor between two dehydrogenases (G6PDH glucose-6-phosphate dehydrogenase and MDH) on DNA nanoscaffolds. c Enhanced enzyme cascade activity by swinging arms. d Improved reaction selectivity by swinging arms. Reproduced from Fu et al. [47], with permission, copyright 2014, Springer Nature

Fig. 11.

Large biomolecular nanostructures organized by artificial swinging arms. a NAD⁺ arms for regulating pathway activity between the G6PDH–MDH cascade and the G6PDH–LDH cascade. Reproduced from Ke et al. [123], with permission, copyright 2016, John Wiley and Sons. b 2D enzyme arrays of the G6PDH–MDH reaction with NAD⁺ swinging arms. Reproduced from Yang et al. [125], with permission, copyright 2018, John Wiley and Sons

DNA-based swinging arms can also facilitate electron transfer in bioelectroactive systems. The research group of Wilner and coworkers used a DNA scaffold to organize the spatial interaction of a GOx enzyme with an electrode surface to generate an anodic electrocatalytic current (Fig. 12a) [126]. In this organized system, a ferrocene-modified ssDNA served as a relay to transfer electrons between the enzyme redox center and the electrode surface. As shown in Fig. 12b, Armand Tepper used DNA scaffolds to organize the electrochemical contact of redox enzymes and the electrode surface by immobilizing the copper enzyme of nitrite reductase (NiR) and its natural electron-exchange partner, pseudoazurin (Paz), onto a gold electrode by DNA scaffold-directed assembly [127]. Electron-transfer patches were realized by conjugating enzymes to specific ssDNA tags that allowed them to swing and perform nitrite reduction by accepting electrons from the gold electrode. As shown in Fig. 12c, Cha and coworkers used DNA scaffolds as a structure-directing template to organize TiO₂ and CdS nanocrystals [128]. Enhanced hydrogen production was achieved when a benzoquinone (BQ)-modified ssDNA was used to transfer electrons between a TiO₂ and a CdS.

Fig. 12.

DNA swinging arms for facilitating bioelectroactive reactions. a A GOx–ferrocene–electrode contact. Reproduced from Piperberg et al. [126], with permission, copyright 2009, American Chemical Society. b A nitrite reductase–pseudoazurin (NiR-Paz) system (SAM self-assembled monolayer). Reproduced from Tepper [127], with permission, copyright 2010, American Chemical Society. c A TiO₂–CdS complex for H₂ production. Reproduced from Ma et al. [128], with permission, copyright 2015, John Wiley and Sons

DNA-based molecular arms have also been useful in engineering nanorobotic systems and assembly lines. The research group of Simmel and coworkers studied the diffusive transport of DNA cargo strands that were bound to a DNA origami surface (Fig. 13a) [129]. These authors concluded that a more rigid DNA arm transferred cargo more efficiently than a more flexible, hinged arm. Based on this result, they developed a nanoscale robotic arm on a rectangular DNA origami tile, the rotation of which was driven and controlled by an electrical field (Fig. 13b) [130]. As shown in Fig. 13c, two research groups, namely those of Zhuang and coworkers and Yin and coworkers, collaborated to develop a DNA origami rotor that was driven by the unwinding function of a helicase (RecBCD complex) during the transcription process [131]. These authors introduced a method of origami-rotor-based imaging and tracking (ORBIT) to track DNA rotation at the single-molecule level with a time resolution of milliseconds.

Fig. 13.

DNA arm-based nanorobotic system. a Double-stranded DNA (dsDNA) arms for fluorescent cargo transport. Reproduced from Kopperger et al. [129], with permission, copyright 2015, American Chemical Society. b A nanoscale robotic arm driven by an electric field. Reproduced from Kopperger et al. [130], with permission, copyright 2018, The American Association for the Advancement of Science. c DNA origami rotor driven by a motor protein (left), atomic force microscopy images of a DNA rotor (middle) and origami-rotor-based imaging and tracking (ORBIT) for tracking DNA rotation (right). Reproduced from Kosuri et al. [131], with permission, copyright 2019, Springer Nature

In addition to swinging arms, DNA nanostructures can also be used to engineer artificial membrane transporters to facilitate the diffusion of ions and small molecules across lipid membranes [36]. Ohmann and co-workers recently designed a synthetic scramblase built from DNA nanostructures [132]. As shown in Fig. 14a, the lipid-scrambling DNA nanostructure was made by the self-assembly of eight ssDNA with two cholesterol prosthetic groups to stabilize the inserted DNA structure in the lipid bilayer. Figure 14b shows molecular dynamic simulations of the lipid scrambling process catalyzed by DNA nanostructures; this DNA-based scramblase could flip 10⁷ lipids per second, which is much faster than a natural enzyme (~ 3 × 10⁴ lipids per second).

Fig. 14.

Synthetic scramblase built from DNA. a The structure of a DNA-based scramblase with two cholesterol prosthetic groups. b Molecular dynamic simulation of the lipid scrambling process. Reproduced from Ohmann et al. [132] under the terms and conditions of the Creative Commons Attribution 4.0 International License, copyright 2018, Springer Nature

DNA scaffolding has also shown its value in more complex synthetic systems. Photosynthesis, for example, is an essential process that provides energy and oxygen for most living organisms on earth. The development of artificial photosynthetic systems, therefore, would present great opportunities in such areas as food and fuel production, energy transformation and catalysis, with broad social and economic impact. DNA nanostructures have been applied to engineering these artificial photosynthetic systems, particularly light-harvesting complexes. As shown in Fig. 15a, Tinnefeld and coworkers were the first to report a multi-fluorophore array on a DNA origami tile; these researchers controlled the spacing distance and the position of each fluorophore to direct the energy transfer [133]. Yan and coworkers constructed an artificial light-harvesting antenna by assembling multiple donor/acceptor pairs on a seven-helix DNA bundle (Fig. 15b) [134]. In this system, stepwise funneling of the excitation energy was directed from the primary donor array (pyrylium [Py] dye) to the acceptor core (Alexa Fluor® [AF] dye) through the intermediate donor (cyanine [Cy3] dye). In a collaboration with the research group of Woodbury and coworkers, Yan and coworkers also assembled a tunable artificial light-harvesting system which used a three-arm DNA nanostructure instead of a the seven-helix bundle (Fig. 15c). This structure was conjugated to a photosynthetic center protein and served as an antenna to transfer energy to the reaction center [135]. Recently, the research groups of Bathe and coworkers and Yan and coworkers worked together to develop a strategy to organize Cy3 dye aggregates on rigid dsDNA scaffolds. These dye/DNA aggregates showed a tunable absorption spectrum and strongly coupled exciton dynamics similar to that of natural light-harvesting systems (Fig. 15d) [136]. These DNA-templated dye aggregates can be used to engineer long-range, directional photo-energy transfer and harvest [137].

Fig. 15.

Artificial photosynthetic systems organized by DNA nanoscaffolds. a Multicolor fluorophore array for photo-energy transfer. Reproduced from Stein et al. [133], with permission, copyright 2011, American Chemical Society. b Artificial light-harvesting network. Reproduced from Dutta et al. [134], with permission, copyright 2011, American Chemical Society. c A DNA-directed light-harvesting/reaction center. Reproduced from Dutta et al. [135], with permission, copyright 2014, American Chemical Society. d A synthetic DNA-based excitonic circuit based on J-aggregates (PIC pseudoisocyanine). Reproduced from Boulais et al. [136], with permission, copyright 2017, Springer Nature

Regulation of Proximity Interactions in Biochemical Reactions

DNA nanostructures can be used to mediate the proximity assembly of enzymes and catalytic cofactors in order to regulate their reaction activities. Ghadiri and coworkers engineered an artificial allosteric enzyme by tethering a metalloprotease with an inhibitor-conjugated ssDNA, which they called an inhibitor-DNA-enzyme (IDE) construct (Fig. 16a) [138]. Due to the flexible ssDNA linker, the inhibitor was able to bind to the active site of an enzyme. The activation of this IDE was triggered by hybridizing the ssDNA linker with a complimentary ssDNA to form a dsDNA segment. The relatively rigid dsDNA blocked the inhibitor from binding to the active site, thus permitting the enzyme to function. This IDE structure was subsequently used to engineer molecular logic circuits by programmable DNA hybridizations [139]. As shown in Fig. 16b, the IDE was used to regulate the fibrinolytic activity that resulted from the binding of a streptokinase (SK) to the plasma proenzyme plasminogen (Pg) [140], with the result being a DNA-linked protease inhibitor bound with a SK–Pg complex that inhibited fibrinolytic activity. Specific DNA inputs disrupted the inhibited binding complex, releasing an active SK–Pg complex. The research group of Merkx and coworkers used DNA-mediated assembly and disassembly to regulate enzyme–inhibitor binding to reversibly switching enzyme activity on and off (Fig. 16c) [141]. As shown in Fig. 16d, Tan and coworkers used a cis–trans photoisomerization of an azobenzene prosthetic group to regulate the binding of a thrombin with its aptamer [142]. In the cis-form of azobenzene, a thrombin was bound to an DNA aptamer which inhibited thrombin-mediated coagulation. Upon UV irradiation, azobenzene switched the from cis-form to the trans-form, exposing a regulatory domain that disrupted the thrombin–aptamer complex, allowing the unbound thrombin to induce blood coagulation [142].

Fig. 16.

DNA hybridization-regulated enzyme activity. a An enzyme–inhibitor interaction (ssDNA Single-stranded DNA). Reproduced from Saghatelian et al. [138], with permission, copyright 2003, American Chemical Society. b Streptokinase–plasminogen (SK–Pg) complex for regulating fibrinolytic activity. Reproduced from Mukherjee et al. [140], with permission, copyright 2018, American Chemical Society. c Enzyme actuation (E enzyme, I inhibitor). Reproduced from Janssen [141], with permission, copyright 2015, American Chemical Society. d Photo-regulated thrombin-aptamer complex. Reproduced from Kim et al. [142], with permission, copyright 2009, National Academy of Sciences

To engineer more complicated regulatory systems, DNA-based nanomachines were developed to regulate the spatial interactions between components of biochemical reactions. Liu and coworkers designed DNA nanotweezers to regulate the spacing distance between a G6PDH and a NAD⁺ cofactor that were anchored on the two arms of DNA tweezers (Fig. 17a) [48]. By switching the DNA tweezers from the open to closed state, the activity of the enzyme and its cofactor was turned on. As shown in Fig. 17b, Liu and coworkers used similar DNA tweezers to regulate the spacing distance between a GOx and HRP with tunable activities [143], while Wilner and coworkers reported DNA nanomachines that could perform “ON/OFF” switchable activation and deactivation of a three‐component biocatalytic cascade (Fig. 17c) [144]. When the tweezers were closed, the cascade reaction was activated by the formation of a hemin/G‐quadruplex‐bridged structure, but when the tweezers were opened, the hemin/G-quadruplex was disrupted. DNA nanotweezers were also used by Kou et al. [145] to regulate the electrochemical response of a GOx/HRP cascade reaction (Fig. 17d). Yang and coworkers constructed a trident-shaped DNA nanoactuator that could switch between four distinct structural conformations [146]. As shown in Fig. 17e, different GOx/HRP activities could be achieved with each conformation of the trident-shaped DNA nanomachine. However, because many enzyme cascade reactions (e.g. GOx/HRP cascade) are not sensitive to enzyme proximity, as discussed previously [92], only small differences of enzyme cascade activities were observed for these four conformations of DNA tweezers. In contrast, DNA nanomachines were more efficient in regulating enzyme/cofactor pairs (which do rely on proximity interaction), with enhanced activities ranging from a few fold up to 100-fold or more [48, 49].

Fig. 17.

DNA nanotweezers-regulated enzyme reaction. a A G6PDH/NAD⁺ pair. Reproduced from Liu et al. [48], with permission. Copyright 2013, Springer Nature. b A GOx/HRP cascade. Reproduced from Xin et al. [143], with permission, copyright 2013, John Wiley and Sons. c A three-component biocatalytic cascade of β-Gal/GOx/hemin. Reproduced from Hu et al. [144], with permission, copyright 2014, John Wiley and Sons. d Distance regulation of a GOx/HRP pair. Reproduced from Kou et al. [145], with permission, copyright 2018, American Chemical Society. e A trident-shaped DNA nanomachine with several conformational states for regulating an enzyme cascade. Reproduced from Xing et al. [146], with permission, copyright 2018, American Chemical Society

Using a simpler approach, Fu and coworkers reported a method of using a DNA hairpin structure to mediate the proximity assembly of biochemical reactions (Fig. 18a) [49]. The self-folded DNA hairpin carried a cofactor that was not able to interact with its partner enzyme, resulting in very low catalytic activity. A triggered opening of the DNA hairpin was subsequently assembled with an enzyme to bring together the enzyme/cofactor pair for actuating the reaction with a 100-fold more activity. Based on this result, a biochemical sensing circuit was designed which combined a sensing module (made of DNA structural switches) with a triggered proximity assembly of an enzyme/cofactor pair. When the sensing module was activated by a target molecule, the enzyme could bind to the cofactor and catalyze a reaction to produce a detectable signal (Fig. 18b). This DNA-based sensing circuit could be used either for detecting microRNA (via strand displacement) or small-molecule metabolites, such as adenosine (using an aptamer) (Fig. 18c). DNA nanostructure-regulated enzyme assemblies provide a new approach to programming enzyme activities. This may lead to the development of a new generation of enzyme-based diagnostic tools and therapeutics. They may also be used as a basis for developing protein feedback loops or allosteric regulation as an alternative or complementary technology to protein engineering.

Fig. 18.

DNA hairpin-mediated proximity assembly of an enzyme and a cofactor. a Enzyme activities for a hairpin-locked cofactor, opened cofactor and co-assembled enzyme/cofactor pair. b A design chart of a biochemical sensing circuit. c Detection of microRNA and adenosine. Reproduced from Oh et al. [49], with permission, copyright 2018, John Wiley and Sons

Conclusions and Future Perspectives

Structural DNA nanotechnology has enabled the design and fabrication of various nano-objects with prescribed geometry and regulated spatial interaction. The combination of DNA nanostructures with enzyme–DNA conjugation provides an efficient approach for engineering artificial biomolecule complexes with finely controlled spatial arrangement and confinement. Considering these advantages together, it can be concluded that DNA nanostructures have the potential to deliver breakthroughs toward the engineering of more sophisticated biomimetic systems, such as synthetic cells, artificial subcellular components and photosynthetic and energy-harvesting structures. For example, DNA scaffolds can be used to organize multilevel assemblies for the construction of a synthetic reactor, including membrane confinement, artificial transmembrane nanopores and encapsulated biochemical reaction pathways [36]. Another potential use of DNA nanotechnology is the design and construction of dynamic and regulated structures with conformational switches triggered by external inputs. Dynamic nanostructures may find utility in the development of feedback-regulated biochemical systems. Some early examples have already demonstrated the feasibility of using DNA nanostructures to regulate enzyme activities, including inhibitor–DNA–enzyme structures, DNA tweezers and DNA swinging arms. It is possible to design substrate cooperativity or product feedback inhibition by incorporating aptamer switches into enzyme inhibition and activation complexes. Finally, diagnostic applications provide great challenges and opportunities to design DNA-based molecular circuits for sensing various molecular targets in vitro or in vivo. Smart DNA circuits can be adapted to various point-of-care diagnosis platforms, such as paper strips and color-change-based assays. This will fit the growing need for fast, sensitive and easy detection of infectious diseases, such as the recent outbreaks of coronavirus, Ebola and Zika virus that resulted in Public Health Emergencies of International Concern as announced by the World Health Organization. Overall, DNA-scaffolded enzyme assemblies will have a bright future and be useful in various applications of biocatalysis, functional biomaterials and novel theranostic medicine.

Abbreviations

BG

Benzylguanine

BQ

Benzoquinone

CH

Chlorohexane

DSS

Disuccinimidyl suberate

DTPC

DNA-templated protein conjugation

DX

Double-crossover DNA tile

G6PDH

Glucose-6-phosphate dehydrogenase

GOx

Glucose oxidase

HRP

Horseradish peroxidase

IDE

Inhibitor–DNA–enzyme

LDH

Lactate dehydrogenase

MDH

Malic dehydrogenase

MTG

Microbial transglutaminase

NHS

N-hydroxysuccinimide

NiR

Nitrite reductase

ORBIT

Origami-rotor-based imaging and tracking

Paz

Pseudoazurin

Pg

Plasminogen

PLP

Pyridoxal 5′-phosphate

SK

Streptokinase

SMCC

Succinimidyl-4-(N-maleimidomethyl) cyclohexane-1-carboxylate

SPDP

Succinimidyl 3-(2-pyridyldithio) propionate

STVs

Streptavidins

TAL

Transcription activator-like

Author Contributions

The manuscript was written through contributions of all authors. All authors have given approval to the final version of the manuscript.

Compliance with Ethical Standards

Conflict of interest

The authors declare no competing financial interest.