scholarly journals Applications of DNA-Functionalized Proteins

2021 ◽  
Vol 22 (23) ◽  
pp. 12911
Author(s):  
Zhaoqiu Gong ◽  
Yuanyuan Tang ◽  
Ningning Ma ◽  
Wenhong Cao ◽  
Yong Wang ◽  
...  
Keyword(s):  
Rapid Development ◽  
Dna Nanotechnology ◽  
Protein Detection ◽  
Protein Assemblies ◽  
Application Process ◽  
Body Protein ◽  
Recognition Ability ◽  
Biological Catalysis ◽  
Structural Dna Nanotechnology ◽  
Artificial Protein

As an important component that constitutes all the cells and tissues of the human body, protein is involved in most of the biological processes. Inspired by natural protein systems, considerable efforts covering many discipline fields were made to design artificial protein assemblies and put them into application in recent decades. The rapid development of structural DNA nanotechnology offers significant means for protein assemblies and promotes their application. Owing to the programmability, addressability and accurate recognition ability of DNA, many protein assemblies with unprecedented structures and improved functions have been successfully fabricated, consequently creating many brand-new researching fields. In this review, we briefly introduced the DNA-based protein assemblies, and highlighted the limitations in application process and corresponding strategies in four aspects, including biological catalysis, protein detection, biomedicine treatment and other applications.

scholarly journals Strategies to Build Hybrid Protein–DNA Nanostructures

Nanomaterials ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1332
Author(s):  
Armando Hernandez-Garcia
Keyword(s):  
Dynamic Systems ◽  
Dna Nanotechnology ◽  
Chemical Properties ◽  
Hybrid Nanostructures ◽  
Advanced Materials ◽  
Dna Nanostructures ◽  
Hybrid Protein ◽  
Structural Protein ◽  
The Individual ◽  
Structural Dna Nanotechnology

Proteins and DNA exhibit key physical chemical properties that make them advantageous for building nanostructures with outstanding features. Both DNA and protein nanotechnology have growth notably and proved to be fertile disciplines. The combination of both types of nanotechnologies is helpful to overcome the individual weaknesses and limitations of each one, paving the way for the continuing diversification of structural nanotechnologies. Recent studies have implemented a synergistic combination of both biomolecules to assemble unique and sophisticate protein–DNA nanostructures. These hybrid nanostructures are highly programmable and display remarkable features that create new opportunities to build on the nanoscale. This review focuses on the strategies deployed to create hybrid protein–DNA nanostructures. Here, we discuss strategies such as polymerization, spatial directing and organizing, coating, and rigidizing or folding DNA into particular shapes or moving parts. The enrichment of structural DNA nanotechnology by incorporating protein nanotechnology has been clearly demonstrated and still shows a large potential to create useful and advanced materials with cell-like properties or dynamic systems. It can be expected that structural protein–DNA nanotechnology will open new avenues in the fabrication of nanoassemblies with unique functional applications and enrich the toolbox of bionanotechnology.

scholarly journals Hybrid Nanoassemblies from Viruses and DNA Nanostructures

Nanomaterials ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 1413
Author(s):  
Sofia Ojasalo ◽  
Petteri Piskunen ◽  
Boxuan Shen ◽  
Mauri A. Kostiainen ◽  
Veikko Linko
Keyword(s):  
Cell Activation ◽  
Immune Cell ◽  
Dna Nanotechnology ◽  
Biological Properties ◽  
Dna Nanostructures ◽  
Dna Structures ◽  
Nanoscale Structures ◽  
Immune Cell Activation ◽  
Wide Range ◽  
Structural Dna Nanotechnology

Viruses are among the most intriguing nanostructures found in nature. Their atomically precise shapes and unique biological properties, especially in protecting and transferring genetic information, have enabled a plethora of biomedical applications. On the other hand, structural DNA nanotechnology has recently emerged as a highly useful tool to create programmable nanoscale structures. They can be extended to user defined devices to exhibit a wide range of static, as well as dynamic functions. In this review, we feature the recent development of virus-DNA hybrid materials. Such structures exhibit the best features of both worlds by combining the biological properties of viruses with the highly controlled assembly properties of DNA. We present how the DNA shapes can act as “structured” genomic material and direct the formation of virus capsid proteins or be encapsulated inside symmetrical capsids. Tobacco mosaic virus-DNA hybrids are discussed as the examples of dynamic systems and directed formation of conjugates. Finally, we highlight virus-mimicking approaches based on lipid- and protein-coated DNA structures that may elicit enhanced stability, immunocompatibility and delivery properties. This development also paves the way for DNA-based vaccines as the programmable nano-objects can be used for controlling immune cell activation.

scholarly journals The Helicity of a DNA-2’-Fluoro DNA Hybrid Duplex Structure

2017 ◽  
Vol 2 (1) ◽  
Keyword(s):  
Double Helix ◽  
Dna Nanotechnology ◽  
Helical Structure ◽  
Hydrogen Atoms ◽  
Atomic Force ◽  
Hybrid Duplex ◽  
Dna Backbone ◽  
Helical Turn ◽  
Dna 2 ◽  
Structural Dna Nanotechnology

Structural DNA nanotechnology is a system whereby branched DNA molecules are fashioned into objects, or 1D, 2D and 3D lattices, as well as nanomechanical devices. Normally, one is dealing with the usual B-form DNA molecule, but variations on this theme can lead to alterations in both the structures and the properties of the constructs. 2’-Fluoro DNA (FDNA), wherein one of the hydrogen atoms of the 2’ carbon is replaced by a fluorine atom, is a minimal steric perturbation on the structure of the DNA backbone. The helical structure of this duplex is of great interest for applications in structural DNA nanotechnology, because the DNA-FDNA hybrid assumes an A-form double helix, without the instabilities associated with RNA. Here we have used an atomic force microscopic method to estimate the helicity of DNA-FDNA hybrids, and we find that the structure contains 11.8 nucleotide pairs per helical turn with an error of ± 0.6 nucleotide pairs, similar to other A-form molecules.

scholarly journals Bio-surface engineering with DNA scaffolds for theranostic applications

2018 ◽  
Vol 4 (1) ◽  
pp. 1-16 ◽  
Author(s):  
Xiwei Wang ◽  
Wei Lai ◽  
Tiantian Man ◽  
Xiangmeng Qu ◽  
Li Li ◽  
...  
Keyword(s):  
Recent Progress ◽  
Surface Engineering ◽  
Dna Nanotechnology ◽  
Three Dimensions ◽  
High Yield ◽  
Biological Applications ◽  
Dna Nanostructures ◽  
Surface Functionality ◽  
Recognition Ability ◽  
Theranostic Applications

Abstract Biosensor design is important to bioanalysis yet challenged by the restricted target accessibility at the biomolecule-surface (bio-surface). The last two decades have witnessed the appearance of various “art-like” DNA nanostructures in one, two, or three dimensions, and DNA nanostructures have attracted tremendous attention for applications in diagnosis and therapy due to their unique properties (e.g., mechanical flexibility, programmable control over their shape and size, easy and high-yield preparation, precise spatial addressability and biocompatibility). DNA nanotechnology is capable of providing an effective approach to control the surface functionality, thereby increasing the molecular recognition ability at the biosurface. Herein, we present a critical review of recent progress in the development of DNA nanostructures in one, two and three dimensions and highlight their biological applications including diagnostics and therapeutics. We hope that this review provides a guideline for bio-surface engineering with DNA nanostructures.

Artificial protein assemblies with well-defined supramolecular protein nanostructures

2021 ◽  
Author(s):  
Suyeong Han ◽  
Yongwon Jung
Keyword(s):  
Vaccine Development ◽  
De Novo ◽  
Building Blocks ◽  
Protein Assembly ◽  
Protein Assemblies ◽  
Cellular Processes ◽  
Wide Range ◽  
Array Structures ◽  
Small Chemical ◽  
Artificial Protein

Nature uses a wide range of well-defined biomolecular assemblies in diverse cellular processes, where proteins are major building blocks for these supramolecular assemblies. Inspired by their natural counterparts, artificial protein-based assemblies have attracted strong interest as new bio-nanostructures, and strategies to construct ordered protein assemblies have been rapidly expanding. In this review, we provide an overview of very recent studies in the field of artificial protein assemblies, with the particular aim of introducing major assembly methods and unique features of these assemblies. Computational de novo designs were used to build various assemblies with artificial protein building blocks, which are unrelated to natural proteins. Small chemical ligands and metal ions have also been extensively used for strong and bio-orthogonal protein linking. Here, in addition to protein assemblies with well-defined sizes, protein oligomeric and array structures with rather undefined sizes (but with definite repeat protein assembly units) also will be discussed in the context of well-defined protein nanostructures. Lastly, we will introduce multiple examples showing how protein assemblies can be effectively used in various fields such as therapeutics and vaccine development. We believe that structures and functions of artificial protein assemblies will be continuously evolved, particularly according to specific application goals.

Square structured photonic crystal fiber based THz sensor design for human body protein detection

2020 ◽  
Author(s):  
Md. Aminul Islam ◽  
Mohammad Rakibul Islam ◽  
Ahmed Mujtaba Al Naser ◽  
Fariha Anzum ◽  
Fatema Zerin Jaba
Keyword(s):  
Photonic Crystal ◽  
Photonic Crystal Fiber ◽  
Human Body ◽  
Protein Detection ◽  
Sensor Design ◽  
Body Protein ◽  
Crystal Fiber ◽  
Thz Sensor

scholarly journals Programming Structured DNA Assemblies to Probe Biophysical Processes

2019 ◽  
Vol 48 (1) ◽  
pp. 395-419 ◽  
Author(s):  
Eike-Christian Wamhoff ◽  
James L. Banal ◽  
William P. Bricker ◽  
Tyson R. Shepherd ◽  
Molly F. Parsons ◽  
...  
Keyword(s):  
Structural Biology ◽  
Energy Transport ◽  
Dna Nanotechnology ◽  
Dna Origami ◽  
Design And Synthesis ◽  
Copy Numbers ◽  
Target Nucleic Acid ◽  
Biophysical Processes ◽  
Fully Automatic ◽  
Structural Dna Nanotechnology

Structural DNA nanotechnology is beginning to emerge as a widely accessible research tool to mechanistically study diverse biophysical processes. Enabled by scaffolded DNA origami in which a long single strand of DNA is weaved throughout an entire target nucleic acid assembly to ensure its proper folding, assemblies of nearly any geometric shape can now be programmed in a fully automatic manner to interface with biology on the 1–100-nm scale. Here, we review the major design and synthesis principles that have enabled the fabrication of a specific subclass of scaffolded DNA origami objects called wireframe assemblies. These objects offer unprecedented control over the nanoscale organization of biomolecules, including biomolecular copy numbers, presentation on convex or concave geometries, and internal versus external functionalization, in addition to stability in physiological buffer. To highlight the power and versatility of this synthetic structural biology approach to probing molecular and cellular biophysics, we feature its application to three leading areas of investigation: light harvesting and nanoscale energy transport, RNA structural biology, and immune receptor signaling, with an outlook toward unique mechanistic insight that may be gained in these areas in the coming decade.

scholarly journals Double cohesion in structural DNA nanotechnology

2006 ◽  
Vol 4 (18) ◽  
pp. 3414 ◽  
Author(s):  
Pamela E. Constantinou ◽  
Tong Wang ◽  
Jens Kopatsch ◽  
Lisa B. Israel ◽  
Xiaoping Zhang ◽  
...  
Keyword(s):  
Dna Nanotechnology ◽  
Structural Dna Nanotechnology
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