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Journal of Nanomedicine & Nanotechnology

Opinion - (2024) Volume 15, Issue 3

Advancing DNA Nanostructures: Streamlined Creation through Chemically Linked Branched DNA for Enhanced Efficiency
Gholamreza Puras*
 
1NanoBioCel Research Group, University of the Basque Country, Paseo de la Universidad, Spain
 
*Correspondence: Gholamreza Puras, NanoBioCel Research Group, University of the Basque Country, Paseo de la Universidad, Spain, Email:

Received: 01-May-2024, Manuscript No. jnmnt-24-25954; Editor assigned: 04-May-2024, Pre QC No. jnmnt-24-25954(PQ); Reviewed: 18-May-2024, QC No. jnmnt-24-25954(QC); Revised: 25-May-2024, Manuscript No. jnmnt-24-25954(R); Published: 31-May-2024, DOI: 10.35248/2157-7439.24.15.732.

Abstract

The construction of advanced DNA nanostructures holds immense potential across diverse fields, yet traditional assembly methods often pose challenges in terms of efficiency and scalability. In this context, the utilization of chemically linked branched DNA presents a promising avenue for streamlining the creation of complex nanoarchitectures in a single step. This article explores the innovative approach of leveraging chemically modified branched DNA building blocks to achieve enhanced efficiency in the assembly of higher-order DNA nanostructures. By enabling precise control over nanostructure architecture and eliminating the need for intermediate purification steps, this technique accelerates progress in DNA nanotechnology. The abstracted approach not only enhances efficiency but also facilitates scalability, opening new avenues for applications in nanomedicine, materials science, and beyond. As researchers continue to refine and expand upon this methodology, the future holds promise for transformative advancements in DNA nanotechnology, shaping the landscape of nanoscale engineering for years to come.

Keywords

DNA nanostructures; Branched DNA; Chemically linked; Streamlined creation; Enhanced efficiency; Nanotechnology

INTRODUCTION

In the realm of nanotechnology, where precision and complexity converge at the molecular level, DNA emerges as a powerful tool for constructing intricate nanostructures. These nanostructures hold immense promise across diverse fields, from medicine to materials science and beyond. However, traditional methods of assembling higher-order DNA nanostructures often involve multiple steps and intricate designs, posing challenges in terms of efficiency and scalability [1,2]. In this article, we explore a novel approach: the streamlined creation of advanced DNA nanostructures through chemically linked branched DNA. By leveraging this innovative technique, researchers can achieve enhanced efficiency in a single step, paving the way for transformative advancements in DNA nanotechnology [3-5]. In the realm of nanotechnology, the construction of complex DNA nanostructures has emerged as a powerful tool with transformative potential across various scientific disciplines [6]. These nanostructures, meticulously designed and engineered at the molecular level, offer unprecedented opportunities for applications in fields ranging from biomedicine to materials science. However, the traditional methods employed for the assembly of higher-order DNA nanostructures often entail multiple steps and intricate design considerations, presenting challenges in terms of efficiency and scalability [7,8]. In response to these challenges, researchers have sought innovative approaches to streamline the creation of advanced DNA nanostructures. Among these approaches, the utilization of chemically linked branched DNA has garnered significant attention for its potential to enhance efficiency and simplify the assembly process. By leveraging chemically modified branched DNA building blocks, researchers aim to achieve precise control over nanostructure architecture while minimizing the complexity of design and synthesis. This article explores the concept of advancing DNA nanostructures through streamlined creation via chemically linked branched DNA, with a focus on enhancing efficiency in the assembly process [9]. We delve into the principles underlying this innovative approach, highlighting its potential to accelerate progress in DNA nanotechnology and unlock new avenues for applications. By elucidating the key concepts and implications of this methodology, we aim to provide insights into the future direction of DNA nanotechnology and its impact on diverse scientific fields [10].

Efficiency through chemically linked branched DNA

At the heart of this streamlined approach lies the concept of chemically linked branched DNA. Unlike traditional methods that rely on sequential assembly steps, chemically linked branched DNA offers a one-pot synthesis strategy, enabling the simultaneous construction of complex nanostructures in a single reaction vessel. This approach streamlines the assembly process, eliminating the need for intermediate purification steps and reducing the overall complexity of design. The key to this technique lies in the design of branched DNA building blocks, which are chemically modified to enable site-specific conjugation. By strategically attaching functional groups to predetermined sites within the DNA sequence, researchers can precisely control the orientation and connectivity of DNA strands, facilitating the assembly of higher-order nanostructures. This precise control allows for the creation of nanostructures with intricate geometries and tailored functionalities, opening up new possibilities for applications in nanomedicine, nanoelectronics, and beyond.

Enhanced efficiency and scalability

The streamlined nature of chemically linked branched DNA assembly offers several advantages over traditional methods. By consolidating multiple assembly steps into a single reaction, researchers can significantly reduce the time and resources required for nanostructure fabrication. This enhanced efficiency not only accelerates the pace of research but also lowers barriers to entry, making DNA nanotechnology more accessible to a broader community of researchers and engineers. Moreover, the scalability of this approach makes it well-suited for large-scale production of DNA nanostructures. Unlike traditional methods that may suffer from diminishing returns or batch-to-batch variability, chemically linked branched DNA assembly can be easily scaled up to meet the demands of industrial-scale manufacturing. This scalability holds promise for applications such as drug delivery, where the production of DNA-based nanocarriers on a large scale is essential for clinical translation.

Applications and future directions

The streamlined creation of advanced DNA nanostructures through chemically linked branched DNA holds tremendous potential across a wide range of applications. In medicine, DNA nanostructures can be engineered to deliver therapeutic payloads with unprecedented precision, targeting specific cells or tissues with minimal off-target effects. In materials science, DNA-based nanostructures can be utilized to create novel materials with tailored properties, such as stimuli-responsive hydrogels or programmable nanocomposites. Looking ahead, future research efforts will focus on further refining and expanding the capabilities of chemically linked branched DNA assembly. By exploring new chemistries, optimizing design strategies, and leveraging advances in computational modeling and simulation, researchers can unlock new frontiers in DNA nanotechnology. Ultimately, the streamlined creation of advanced DNA nanostructures represents a paradigm shift in the field, offering a pathway towards the rapid development and deployment of next-generation nanotechnologies.

CONCLUSION

In conclusion, the streamlined creation of advanced DNA nanostructures through chemically linked branched DNA heralds a new era of efficiency and scalability in DNA nanotechnology. By consolidating multiple assembly steps into a single reaction and enabling precise control over nanostructure architecture, this innovative approach accelerates progress towards the realization of complex DNA-based systems with transformative applications. As researchers continue to push the boundaries of nanoscale engineering, the future holds promise for even greater advancements in DNA nanotechnology, shaping the landscape of science and technology for years to come. By consolidating multiple assembly steps into a single reaction and minimizing the need for intermediate purification, this innovative approach accelerates the pace of research and facilitates scalability. Moreover, the enhanced efficiency of chemically linked branched DNA assembly opens up new possibilities for applications in diverse fields, including nanomedicine, materials science, and nanoelectronics. Looking ahead, future research efforts will focus on further refining and expanding upon this methodology, exploring new chemistries, and optimizing design strategies to unlock the full potential of DNA nanotechnology. By continuing to push the boundaries of nanoscale engineering, researchers can harness the power of DNA nanostructures to address pressing challenges and drive innovation across a wide range of disciplines.

REFERENCES

  1.  Shi Y, van Steenbergen M J, Teunissen A J P, van der Meel R, Lammers T. Drug delivery strategies for platinum-based anticancer drugs. Expert Opin Drug Deliv. 2020; 17(5): 587-604.
  2. Indexed at, Google Scholar, Crossref

  3. Ma D, Zhang, H B, Shu W. Integration of a Nanocarrier-Based Platform for Dual-Responsive Cocktail Chemotherapy and Dual-Modal Imaging. Advanced Materials. 2019; 31(12): 1807887.
  4. Indexed at, Google Scholar, Crossref

  5. Hobbs S K, Monsky, W L, Yuan F, Roberts W G, Griffith L, et al. Regulation of transport pathways in tumor vessels: Role of tumor type and microenvironment. Proc Natl Acad Sci. 2018; 95(8): 4607-4612.
  6. Indexed at,  Google Scholar, Crossref

  7. Dong Y, Love K T, Dorkin J R, Sirirungruang S, Zhang Y, Chen D,  et al. Lipopeptide nanoparticles for potent and selective siRNA delivery in rodents and nonhuman primates. Proc Natl Acad Sci. 2018; 111(11): 3955-3960.
  8. Indexed at, Google Scholar, Crossref

  9. Li Y, Wang Y, Huang G, Gao J, Cooper I R, Ji J, et al. Recent progress in smart drug delivery nanosystems using stimuli-responsive polymers. J Mater Chem B. 2019; 7(8): 1139-1161.
  10. Indexed at, Google Scholar, Crossref

  11. Miao L, Huang L, Exploring N. Nano-enabled delivery of RNAi and CRISPR-Cas9 for cancer treatment. Nano Today. 2020; 32: 100853.
  12. Indexed at, Google Scholar, Crossref

  13. Wang Z, Li X, Ying Z. Combining Magnetic Nanoparticles and Ultrasound for Drug Delivery in Cancer: A Comprehensive Review. Crit Rev Oncol Hematol. 2018; 131: 34-49.
  14. Indexed at, Google Scholar, Crossref

  15. Qin B, Pei J, Guo H, Dong X, Zong B, Li D. Bioinspired nanoparticles for direct intratumoral chemotherapy of local cancer. J Mater Chem B. 2019; 7(23): 3646-3652.
  16. Google Scholar, Crossref

  17. Lentacker I, Geers B, Demeester J. De Smedt, S. C. Advanced Delivery Strategies for Anticancer Nanomedicine. Nanomedicine. 2021; 7(2): 179-196.
  18. Indexed at, Google Scholar, Crossref

  19. Kieran D, Woods A, Villalta-Cerdas A, Weiner S. Tumor-associated antigens for the induction of antitumor immune responses. Annual Review of Immunology. 2020; 39: 251-272.
  20. Google Scholar, Crossref

Citation: Gholamreza P (2024) Advancing DNA Nanostructures: Streamlined Creation through Chemically Linked Branched DNA for Enhanced Efficiency. J Nanomed Nanotech. 15: 732.

Copyright: ©2024 Gholamreza P. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.