The video outlines the process of self-assembling DNA origami structures using a specific mixture of scaffold and oligonucleotide staples. It details preparation, annealing procedures, purification using filtration, and collection steps, concluding with atomic force microscopy imaging to verify proper assembly, noting challenges in visualizing certain structural features.

dna origami fork assembly for dna origami nanoantenna (dona)

Plasmonic DNA Origami Nanoantennas로 가능한 단일 분자 SERS 측정

DNA origami is a nanotechnology technique that involves folding DNA strands into specific shapes and patterns. The ability to create structures with precise control at the nanoscale is one of the key advantages of DNA origami1. The ability to manipulate matter at such a small scale has the potential to revolutionize a wide range of fields, including medicine, electronics, and materials science2. For example, DNA origami structures have been used to deliver drugs directly to cancer cells3,4, create nanoscale sensors for detecting diseases5,6, and create intricate patterns on the surfaces of materials6,7. Furthermore, the ability to use DNA origami to create complex nanoscale structures has created new opportunities for studying fundamental biological processes at the nanoscale8.
Surface enhanced Raman scattering (SERS) is a robust analytical technique that detects and identifies molecules at extremely low concentrations9. It is based on the Raman effect, which is a change in the wavelength of scattered light10. SERS requires a plasmonic metal substrate to enhance the Raman signal of molecules adsorbed onto it. This enhancement can be up to 1011 times greater than the signal obtained from the same molecule measured by conventional Raman spectroscopy, making SERS a highly sensitive method for analyzing trace amounts of substances11.
The Raman signal enhancement of nanoparticles is mostly due to electromagnetic enhancement based on the excitation of localized surface plasmon resonance (LSPR)12. In this phenomenon, electrons within the metal nanoparticle oscillate collectively around the surface of the metal nanoparticle during light incidence. This results in the creation of a standing wave of electrons known as a surface plasmon, which can resonate with the incident light. The LSPR greatly enhances the electric field near the particle&#39;s surface, and the optical absorption of the particle is maximum at the plasmon resonant frequency. The surface plasmon&#39;s energy depends on the shape and size of the metal nanoparticle, as well as the properties of the surrounding medium13. A higher enhancement could be further achieved by plasmonic couplings, such as when two nanoparticles are close to each other at a distance of approximately 2.5 times the diameter length or less14. The proximity causes the LSPR of both nanoparticles to interact with each other, enhancing the electric field in the gap between the particles by several orders of magnitude, far exceeding the enhancement of a single nanoparticle15,16,17. The magnitude of the enhancement is inversely proportional to the distance between the nanoparticles; as the distance decreases, a critical point appears where the enhancement is sufficient to detect single molecules (SMs)18.
DNA origami represents a key technology that can efficiently arrange plasmonic nanoparticles to exploit and optimize the plasmonic coupling19. At the same time, molecules of interest can be placed precisely at the place where optical detection is most efficient. This has been demonstrated with DNA origami-based plasmonic nanoantennas for fluorescence detection20. In contrast to the detection of fluorescent labels, SERS provides the possibility to detect a direct chemical fingerprint of a molecule, making the single-molecule SERS very attractive for sensing as well as monitoring chemical reactions and mechanistic studies. DNA origami can also be used as a mask to fabricate plasmonic nanostructures with well-defined shapes21, although the possibility to position target molecules precisely into the hot spot is then lost.
Using colocalized atomic force microscopy (AFM) and Raman measurements, we can obtain the Raman spectra from a single DNA origami nanoantenna (DONA) and potentially a single molecule if placed at the position of highest signal enhancement. The DONA comprises a DNA origami fork and two precisely positioned nanoparticles, fully coated with DNA complementary to extended staple strands attached to the DNA origami. Upon DNA hybridization, the nanoparticles are bound to the DNA origami fork with a 1.2-2.0 nm gap between the nanoparticle surfaces22. Such assembly creates a hot spot in between the nanoparticles with a signal enhancement of up to 1011-fold, as calculated from finite difference time domain (FDTD) simulations22, thus permitting SM SERS measurements. However, the volume of the highest enhancement is small (in the 1-10 nm3 range), and consequently the target molecules need to be positioned precisely into this hot spot. The DNA origami fork allows the positioning of a single molecule between the two nanoparticles using a DNA fork bridge and suitable coupling chemistry. Nevertheless, observing such SMs in Raman spectra is very challenging22. Alternatively, the nanoparticles can be fully coated with the target molecule, such as a TAMRA dye, to allow for single DONA measurements with a higher SERS intensity21. In this case, the TAMRA is covalently attached to the DNA coating strand (Figure 1).

저자 스포트라이트: Single-molecule Surface-Enhanced Raman Scattering Measurements Enabled by Plasmonic DNA Origami Nanoantennas  

플라즈몬 DNA 종이접기 나노안테나로 구현되는 단일 분자 표면 강화 라만 산란 측정

Our research aims to develop new tools to detect single molecules by surface-enhanced Raman scattering or source. This is the only technique that provides a chemical fingerprint of a molecule and is sensitive enough to detect single molecules. In this way, detailed mechanistic information about chemical reactions can be obtained.DNA origami nanostructures have been used to precisely position both plasmonic nanoparticles and target molecules. And this is required because the enhanced Raman scattering originates from a small nanometric volume between the nanoparticles which we call hotspots. And we have now created new plasmonic DNA origami nanoantenna, exactly for this purpose.The main challenge is to place target molecules in such hotspots between two nanoparticles and collect Raman data from exactly one nanoantenna structure. To collect large amounts of data and efficient correlation between atomic force microscopy an Raman spectroscopy needs to be done. The plasmonic DNA origami nanoantennas allow for a reproducible production of a large number of plasmonic dimers in which the target molecule is precisely positioned in between the nanoparticles in the hotspot.And through a correlation of the AFM and Raman data, we can now make sure that there's only a single molecule that is detected. Now we can track single molecules such as dye molecules or proteins in real time, and their behavior in the hotspots and their reactions to chemical changes in the environment. For example, the change of the spin state of single human molecules was recently monitored.In the future, we aim to monitor chemical reactions at the single molecular level and to study their reaction mechanisms. In addition, we can use this technology to detect medically-relevant biomolecules with very high sensitivity.

Watch this Scientific Journal Video about DNA Origami Fork Assembly for DNA Origami Nanoantenna DONA at JoVE.com

DNA Origami Fork Assembly for DNA Origami Nanoantenna (DONA)  

DNA 종이 접기 나노 안테나 (DONA)에 대한 DNA 종이 접기 포크 어셈블리

하나의 포트에서 DNA 종이접기 구조를 자가조립하기 위해, 15 밀리몰 염화마그네슘으로 보충된 TAE 완충액 중의 원형 스캐폴드 가닥 M13mp18 및 100 나노몰의 201 짧은 올리고뉴클레오티드 스테이플의 혼합물을 제조하는 것으로 시작한다. 그런 다음 초순수를 사용하여 용액의 총 부피를 100 마이크로 리터로 조정하십시오. 온도 구배를 사용하여 열순환기에서 용액을 어닐링합니다.섭씨 80도까지 빠르게 가열하는 것으로 시작하고 표시된 온도 구배 프로그램을 단계별로 따르십시오. 과량의 스테이플로부터 혼합물을 정제하기 위해, 100 마이크로리터의 DNA 종이접기 용액을 100 킬로달톤 분자량 컷오프 아미콘 필터에 첨가한다. 그런 다음 400 마이크로 리터의 초순수를 첨가합니다.그 후 실온에서 8분 동안 6, 000G에서 원심분리한다. 원심분리 후 필터를 제거하고 튜브를 뒤집어 여과액을 버립니다. 앞에서 설명한 대로 400마이크로리터의 초순수를 필터와 원심분리기에 추가합니다.정제된 나노구조체 용액을 수집하였다. 새 튜브에서 필터를 거꾸로 뒤집고 제조업체의 지침에 따라 실온에서 2 분 동안 1, 000G에서 원심 분리합니다. DNA 종이 접기 포크의 적절한 조립은 원자력 현미경 또는 AFM 이미징을 사용하여 보장되었습니다.예상대로 대부분의 포크는 팔이 부러지지 않고 견고했습니다. 그러나 팔 사이의 다리는 직경이 작고 유연성이 높기 때문에 이미지화하기가 어려웠습니다.

dna-origami-fork-assembly-for-dna-origami-nanoantenna-dona

Research

JoVE Journal

Chemistry

DNA Origami Fork Assembly for DNA Origami Nanoantenna (DONA)

483 조회수.  University of Potsdam. 하나의 포트에서 DNA 종이접기 구조를 자가조립하기 위해, 15 밀리몰 염화마그네슘으로 보충된 TAE 완충액 중의 원형 스캐폴드 가닥 M13mp18 및 100 나노몰의 201 짧은 올리고뉴클레오티드 스테이플의 혼합물을 제조하는 것으로 시작한다. 그런 다음 초순수를 사용하여 용액의 총 부피를 100 마이크로 리터로 조정하십시오. 온도 구배를 사용하여 열순환기에서 용액을 어닐링합니다.

비디오: DNA Origami Fork Assembly for DNA Origami Nanoantenna (DONA)  

Single-Molecule Surface-Enhanced Raman Scattering Measurements Enabled by Plasmonic DNA Origami Nanoantennas

Surface-enhanced Raman scattering (SERS) has the capability to detect single molecules for which high field enhancement is required. Single-molecule (SM) SERS is able to provide molecule-specific spectroscopic information about individual molecules and therefore yields more detailed chemical information than other SM detection techniques. At the same time, there is the potential to unravel information from SM measurements that remain hidden in Raman measurements of bulk material. This protocol outlines the SM SERS measurements using a DNA origami nanoantenna (DONA) in combination with atomic force microscopy (AFM) and Raman spectroscopy. A DNA origami fork structure and two gold nanoparticles are combined to form the DONAs, with a 1.2-2.0 nm gap between them. This allows an up to 1011-fold SERS signal enhancement, enabling measurements of single molecules. The protocol further demonstrates the placement of a single analyte molecule in a SERS hot spot, the process of AFM imaging, and the subsequent overlaying of Raman imaging to measure an analyte in a single DONA.

This protocol demonstrates single-molecule surface-enhanced Raman scattering (SERS) measurements using a DNA origami nanoantenna (DONA) combined with colocalized atomic force microscopy (AFM) and Raman measurements.

Surface-enhanced Raman scattering (SERS) has the capability to detect single molecules for which high field enhancement is required. Single-molecule (SM) ...

연구

화학

To self-assemble the DNA origami structure in one pot begin by preparing a mixture of 2.5 nanomolar of the circular scaffold strand M13mp18 and 100 nanomolar of the 201 short oligonucleotide staples in TAE buffer supplemented with 15 millimolar magnesium chloride. Then adjust the total volume of the solution to 100 microliters using ultrapure water. Anneal the solution in a thermocycler using a temperature gradient.Start by rapidly heating to 80 degrees Celsius and follow the displayed temperature gradient program step by step. To purify the mixture from excess staples add 100 microliters of the DNA origami solution to a 100 kilodalton molecular weight cutoff amicon filter. Followed by adding 400 microliters of ultrapure water.Then centrifuge at 6, 000G for eight minutes at room temperature. After centrifuging, remove the filter and flip the tube to discard the filtrate. Add 400 microliters of ultrapure water to the filter and centrifuge as demonstrated previously.To collect the purified nanostructure solution. Flip the filter upside down in a new tube and centrifuge at 1, 000G for two minutes at room temperature following the manufacturer's instructions. Proper assembly of the DNA origami fork was ensured using atomic force microscopy or AFM imaging.As expected, most forks were solid with no broken arms. However, the bridge between the arms was difficult to image because of its small diameter and high flexibility.

DNA Coating of Gold Nanoparticle (AuNP) for DNA Origami Nanoantenna (DONA)

To coat the gold nanoparticles with DNA, take 400 microliters of commercially obtained gold nanoparticle solution and centrifuge it at 3, 500G at room temperature for five minutes. Using a pipette, remove the supernatant and resolubilize the pellet in 25 microliters of UltraPure water. Next, add four microliters of commercially obtained 100 micromolar thiol modified DNA.Add one microliter of 100 millimolar TCEP solution. Incubate the mixture for 10 minutes at room temperature. Following incubation, add five microliters of the mixture to the previously concentrated gold nanoparticle solution.Vortex the resulting mixture for five seconds and freeze for at least two hours at minus 20 degrees Celsius. After thawing the frozen mixture at room temperature, centrifuge the same at 3, 500G for five minutes at room temperature to remove excess added DNA coating. Using a pipette, remove the supernatant and resolubilize the pellet in 10 microliters of water.The changing color of the solution at each step indicated proper coating of the gold nanoparticle. The deep red color of the gold nanoparticles changed to dark purplish red as soon as the DNA was added. Freezing changed the color to purple, and thawing returned it to deep red.The absorbance spectra of the 60 nanometer DNA coated gold nanoparticles showed a shift in absorbance peak compared to that of the bare gold nanoparticles.

DNA 종이 접기 나노 안테나 (DONA)를위한 금 나노 입자 (AuNP)의 DNA 코팅

DNA Origami Nanoantenna (DONA) Assembly and Gel Electrophoresis

To assemble the DNA origami nanoantennas or DONAs use the DNA-coated gold nanoparticles and the already assembled DNA origami forks. Add the nanofork solution to the coated gold nanoparticle solution maintaining a final molar concentration ratio of 1.5 is to one. To the mixture add magnesium chloride from a 50 millimolar stock solution to reach a final magnesium chloride concentration of four millimolar.Adjust the final volume to 20 microliters using ultrapure water. Hybridize the DONAs using a temperature gradient in a thermocycler. Starting with rapid heating to 40 degrees Celsius follow the displayed temperature gradient program step by step.For purification of the DONAs prepare 1%agarose gel by dissolving 0.8 grams of agarose in 80 milliliters of T A E supplemented with five millimolar magnesium chloride. Add 2.25 microliters of loading buffer containing 30%glycerol and 13 millimolar magnesium chloride to 18 microliters of DONA solution. Run the gel for 60 minutes at 70 volts in an ice water bath.Cut out the band of interest and place it on a microscopy slide wrapped with paraffin plastic film. Then squeeze out the solution using a second paraffin film-wrapped microscopy slide. Using a pipette collect the squeezed liquid into a 500 microliter tube.During the agarose gel purification, a dimer band corresponding to the DONAs appeared above the free gold nanoparticles band, the fastest running band in the sample.

DNA 종이 접기 나노 안테나 (DONA) 조립 및 겔 전기 영동

Colocalization of AFM and Raman Measurements on DNA Origami Nanoantenna (DONA)

To perform colocalized AFM imaging and Raman measurements on the purified DNA origami nanoantenna, or DONA. first treat a silicone chip with plasma for 10 minutes. Incubate 10 microliters of the purified DONA solution and 10 microliters of 100 millimolar magnesium chloride on the chip for three hours.Then wash the chip two times with an ethanol-water mixture and blow dry with compressed air. Tape the dried chip on a magnetic disc and insert it into the instrument for atomic force microscopy or AFM imaging. Next, choose the desired laser wavelength, power, and accumulation time for the Raman measurements.For gold nanoparticle fully coated with TAMRA, select a 633 nanometer laser, 100 microwatt power, and one second integration time. For a single TAMRA measurement, change to 400 microwatt power and four second integration time. After adjusting the parameters, place the cursor on top of the desired DONA in the AFM image.Then start the Raman measurement. For colocalization measurements, AFM imaging of the sample was performed to locate the DONAs. Following that, Raman spectra from single DONAs were collected and compared to ensure that the spectra obtained were from TAMRA molecules.The main TAMRA peaks were visible in the fully coated TAMRA gold nanoparticle, although the signal-to-noise ratio for the single molecule TAMRA spectra was lower, the main peaks were identifiable.