Revision as of 16:07, 17 October 2018

Strand 5 for in-vivo synthesis of Nano Drug Carrier

This part encodes a component strand of our originally designed Nano Drug Carrier (NDC). The strand-encoding region is followed by an HIV-terminator binding site (HTBS). This component strand can be expressed in the presence of HIV reverse transcriptase and murine leukaemia virus reverse transciptase inside E. coli DH5alpha (Elbaz, 2016).

Sequence and Features

Introduction

Biology

Part structure

This biobrick is part of a DNA nanostructure production system we named ETHERNO (E. coli-synthesized Therapeutic Nanostructures). Each of the biobrick submitted encodes a single-stranded DNA of specific sequence. These ssDNA synthesized can then be extracted for assembly of our originally designed therapeutic nanostructure.

In each biobrick, the component strand encoding region is followed by an HTBS, a stemloop for binding of HIV reverse transcriptase and B0054, a strong terminator. For our design to function, these three structural components must be together as a basic part. This part design is modified from a previously described method of ssDNA synthesis using this HTBS sequence and B0054 terminator.^[1] Each component strand encoding region is originally designed, with component strand sequence generated by 3D nanostructure simulation in the software TIAMAT. ^[2]

For nanostructures composed of multiple DNA strands of different sequences, the BioBricks required follow the same basic structure as shown in Fig. 1.

Figure 1. ETHERNO workflow

Therapeutic DNA nanostructure

Design principles: safety, efficient cell entry, flexibility, stability

In this project, 2 DNA nanostructures, namely Nano Drug Carrier (NDC) and Nano Drug Carrier-AS1411 (NDC-AS) for breast cancer therapy were designed and tested. Each nanostructure is made up of 5 single-stranded DNA synthesized using 5 different BioBricks. The 2 nanostructures have 2 componant strands in common, so a total of 8 BioBricks were made and submitted.

Our Nano Drug Carriers are composed entirely of DNA, which is non-toxic and degradable inside human cells. The Nano Drug Carriers are designed as tetrahedrons to facilitate cell entry. Previous studies have shown that three-dimensional DNA nanostructure enter mammalian cells more efficiently than two-dimensional AS1411 or linear structures. ^[3] Tetrahedron is chosen because we consider it the simplest three-dimensional structure, which can be easily assembled from just a few DNA strands. Building the Nano Drug Carrier with separate DNA strands means that much flexibility is allowed for functional modifications. Functional DNA sequences can be conveniently added to the 4 vertices of the tetrahedron to achieve oligonucleotide delivery or cell antigen binding, enhancing the effect of the drug. Three-dimensional structures composed of double stranded DNA have been shown to be stable in extracellular compartment, making them ideal as drug carriers.Cite error: Invalid <ref> tag; refs with no name must have content

Figure 2. NDC

refs with no name must have content Part of Strand 5 is a displacement toehold complimentary to miR21. The 5' segment next to the toehold is complimentary to another target, miR217. The 3' segment binds complimentarily to 5' end of Strand 1. Breast cancer drug, doxorubicin (Dox) can be loaded onto the tetrahedron by DNA intercalation.Cite error: Invalid <ref> tag; refs with no name must have content Therapeutic functions are expected to be exerted in two ways: cancer miRNA down-regulation by the displaced strand and intracellular release of doxorubicin.

Figure 3. NDC-AS

refs with no name must have contentAs nucleolin is overexpressed in breast cancer cells, NDC-as was expected to preferentially enter cancer cells and demonstrate better entry and cancer cell cytotoxicity than NDC.Cite error: Invalid <ref> tag; refs with no name must have content The complimentary region between the tetrahedral base and the strand to be displaced was also extended to increase displacement specificity.

Characterization

Device

To test the feasibility of our designs, chemically synthesized DNA oligos of the sequences generated by Tiamat were used to assemble the NDCs. DNA-21 and DNA-217, which are DNA equivalents of miR21 and miR217 were initially used as the inputs, before using RNA. Native polyacrylamide gel electrophoresis (PAGE) was used to visualize the component strands and the assembled NDCs.

Figure 4.PAGE (8%) image of NDC component single strands, DNA inputs and assembled NDC

After assembly, component strands were seen to have formed complexed too large to be run through the gel PAGE (Fig.4). These large complexes close to the loading well were expected to be successfully assembled NDC that could not pass through the gel due to its large 3D structure, with a tetrahedral base of around 16nm per edge. The band of around 20bp seen below NDC were unbound Strand 5, which was designed to be only partially complementary to Strand 1.

Figure 5. PAGE (8%) images showing annealed strands of various combinations. Three-dimensional NDCs are seen to be of much a larger band size than incomplete two-dimensional structures.

To confirm the assembly of NDC from the 5 component strands, PAGE of structures formed by different strand combinations was done (Fig.5). After annealing, component strands formed complexes larger than their individual sizes, proving DNA structure assembly due to base complementarity. Large complexes close to the bottom of wells could only be seen in samples containing Strand 1, 2, 3 and 4, which together form the 3D tetrahedral base of NDC. These results supported the successful formation of a specific 3D DNA structure.

Figure 6. PAGE (8%) showing strand displacement by DNA equivalents of miRNA target A and B after 30 minutes incubation at 37°C. Displacement of strand 5 out of NDC by the targets are visualized as bands of size 40 to 50bp in lane 3 to lane 5. Table shows relative band intensities compared against expected Output for preliminary displacement efficiency evaluation.

Our NDC was designed to release to an anti-microRNA oligonucleotide upon binding with intracellular miR21 and miR217. As a preliminary test of strand displacement efficiency, we incubated DNA-21 and DNA-217 with NDC in phosphate buffered saline at 37C and ran a page (Fig.6). Successful strand displacement is shown, because when displaced by 2 inputs, a band of the correct output size was produced and the band intensity, correlated with DNA concentration, was higher than when displaced by either 1 of the inputs.

Parts application

References

1. ↑ Elbaz et al. (2016). Genetic encoding of DNA nanostructures and their self-assembly in living bacteria. Nat Commun. 7:11179.
2. ↑ Williams et al. (2008). Tiamat: a three- dimensional editing tool for complex DNA structures. DNA Computing. DNA 2008. Lecture Notes in Computer Science. 5347; 90-101.
3. ↑ Charoenphol, P. & Bermudez, H. (2014, April). Design and Application of Multifunctional DNA Nanocarriers for Therapeutic Delivery. Acta Biomaterialia, 10(4),1683-1691.