98%
921
2 minutes
20
The concept of micrometer-scale swimming robots, also known as microswimmers, navigating the human body to perform robotic tasks has captured the public imagination and inspired researchers through its numerous representations in popular media. This attention highlights the enormous interest in and potential of this technology for biomedical applications, such as cargo delivery, diagnostics, and minimally invasive surgery, as well as for applications in microfluidics and manufacturing. To achieve the collective behavior and control required for microswimmers to effectively perform such actions within complex, in vivo and microfluidic environments, they must meet a strict set of engineering criteria. These requirements include, but are not limited to, small size, structural monodispersity, flexibility, biocompatibility, and multifunctionality. Additionally, microswimmers must be able to adapt to delicate environments, such as human vasculature, while safely performing preprogrammed tasks in response to chemical and mechanical signals. Naturally information-bearing biopolymers, such as peptides, RNA, and DNA, can provide programmability, multifunctionality, and nanometer-scale precision for manufactured structures. In particular, DNA is a useful engineering material because of its predictable and well-characterized material properties, as well as its biocompatibility. Moreover, recent advances in DNA nanotechnology have enabled unprecedented abilities to engineer DNA nanostructures with tunable mechanics and responsiveness at nano- and micrometer scales. Incorporating DNA nanostructures as subcomponents in microswimmer systems can grant these structures enhanced deformability, reconfigurability, and responsiveness to biochemical signals while maintaining their biocompatibility, providing a versatile pathway for building programmable, multifunctional micro- and nanoscale machines with robotic capabilities. In this Account, we highlight our recent progress toward the experimental realization of responsive microswimmers made with compliant DNA components. We present a hybrid top-down, bottom-up fabrication method that combines templated assembly with structural DNA nanotechnology to address the manufacturing limitations of flexibly linked microswimmers. Using this method, we construct microswimmers with enhanced structural complexity and more controlled particle placement, spacing, and size, while maintaining the compliance of their DNA linkage. We also present a novel experimental platform that utilizes two-photon polymerization (TPP) to fabricate millimeter-scale swimmers (milliswimmers) with fully customizable shapes and integrated flexible linkers. This platform addresses limitations related to population-level heterogeneity in micrometer-scale systems, allowing us to isolate the effects of milliswimmer designs from variations in their physical dimensions. Using this platform, we interrogate established hydrodynamic models of microswimmer locomotion and explore how design and actuation parameters influence milliswimmer velocity. We next explore opportunities for enhancing microswimmer responsiveness, functionality, and physical intelligence through the inclusion of nucleic acid subcomponents. Finally, we highlight how our parallel research on xeno nucleic acids and interfacing DNA nanotechnology with living cells can enable the creation of fully organic, truly biocompatible microswimmers with enhanced functionality, improving the viability of microswimmers for applications in healthcare, manufacturing, and synthetic biology.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12379156 | PMC |
http://dx.doi.org/10.1021/accountsmr.5c00009 | DOI Listing |
Mikrochim Acta
September 2025
Department of Public Health Laboratory Sciences, College of Public Health, Hengyang Medical School, University of South China, 28 Changsheng West Road, Hengyang, 421001, Hunan, China.
We systematically evaluated the DNA adsorption and desorption efficiencies of several nanoparticles. Among them, titanium dioxide (TiO₂) nanoparticles (NPs), aluminum oxide (Al₂O₃) NPs, and zinc oxide (ZnO) NPs exhibited strong DNA-binding capacities under mild conditions. However, phosphate-mediated DNA displacement efficiencies varied considerably, with only TiO₂ NPs showing consistently superior performance.
View Article and Find Full Text PDFMol Pharm
September 2025
Division of Pharmaceutics and Pharmacology, College of Pharmacy; Center for RNA Nanotechnology and Nanomedicine; James Comprehensive Cancer Center, College of Medicine, The Ohio State University, Columbus, Ohio 43210, United States.
Liver cancer, particularly hepatocellular carcinoma (HCC), poses significant treatment challenges due to chemoresistance and cancer recurrence. Similar to customs at the border, the liver detoxifies incoming chemicals via efflux pumps and overexpresses ATP-binding cassette (ABC) drug exporters, leading to chemoresistance. ABC contains a multihomosubunit structure and a revolving transport mechanism, actively effluxing drugs from cancer cells, thereby reducing intracellular drug accumulation and therapeutic efficacy.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
September 2025
Changchun Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Changchun 130122, China. Electronic address:
To achieve ultrasensitive and real-time detection of the H1N1 influenza virus, this study designed a nucleic acid-free fluorescent biosensor based on 3D spherical DNA nanostructure and CRISPR/Cas12a (3D-SDNC). The biosensor constructs a rigid 3D nano-framework via self-assembly of six oligonucleotide chains, with H1N1-specific nucleic acid aptamers and Cas12a activator strands strategically positioned at multi-spined vertices for precise spatial coupling between viral recognition and signal transduction. Upon aptamer-virus binding, the induced conformational change liberates the activator strand, thereby activating the trans-cleavage activity of the Cas12a/crRNA complex to efficiently cleave the HEX/BHQ1 double-labeled fluorescent probe and initiate cascade signal amplification.
View Article and Find Full Text PDFMed Sci (Paris)
September 2025
Biologiste, généticien et immunologiste, Président d'Aprogène (Association pour la promotion de la Génomique), 13007, Marseille, France.
DNA sequencing using nanopores is now well established. Could the approach be extended to proteins ? There are a number of difficulties but work by many groups has shown proof-of-principle solutions for most of them. Further progress could indeed lead to a workable protein sequencing approach that would have many applications in research and in the clinic.
View Article and Find Full Text PDFSmall Methods
September 2025
Institute of Analytical Chemistry and Instrument for Life Science, The Key Laboratory of Biomedical Information Engineering of Ministry of Education, School of Life Science and Technology, Xi'an Jiaotong University, Xianning West Road, Xi'an, Shaanxi, 710049, P. R. China.
Anisotropic gold nanoparticles (AuNPs) exhibit unique physicochemical properties that render them highly valuable for diverse applications. However, precise control over their growth direction and number of branches is challenging with conventional synthesis methods. A DNA origami-templated enzymatic synthesis strategy addresses this limitation.
View Article and Find Full Text PDF