Christopher C. Perry, Reinhard W. Schulte, Salma Khan, Kevin E. Nick, Jacob M. Holley, Jamie R. Milligan
{"title":"Inclusion of silver nanoparticles into condensed DNA","authors":"Christopher C. Perry, Reinhard W. Schulte, Salma Khan, Kevin E. Nick, Jacob M. Holley, Jamie R. Milligan","doi":"10.1007/s11051-025-06307-0","DOIUrl":null,"url":null,"abstract":"<div><p>Ionizing radiation is widely used as a therapeutic tool. There is interest in the use of metallic nanoparticles in the role of radiation sensitizer. We have previously described an experimental system in which plasmid DNA condensed with basic oligopeptides functions as a model for chromatin. This system reproduces well the yields of DNA radiation damage observed in mammalian cells. We aimed here to extend this model system by including silver nanoparticles. Spectroscopy, light scattering, gel electrophoresis, sedimentation, and atomic force microscopy all indicate that anionic lipoate-coated silver nanoparticles can be co-aggregated with DNA by using a tetra-arginine peptide. The resulting co-aggregates are micron sized, of the same order as the nuclei of mammalian cells. Increasing the ionic strength results in disaggregation enabling recovery of the freed DNA after which it can be subjected to a wide variety of assays to characterize the radiosensitizing effects of the silver nanoparticles. This self-assembled system of three ionically bound components (nanoparticle, DNA, and peptide) offers the advantage of avoiding the complexity of forming and breaking covalent bonds between the nanoparticles and DNA.</p></div>","PeriodicalId":653,"journal":{"name":"Journal of Nanoparticle Research","volume":"27 5","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2025-04-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Nanoparticle Research","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s11051-025-06307-0","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Ionizing radiation is widely used as a therapeutic tool. There is interest in the use of metallic nanoparticles in the role of radiation sensitizer. We have previously described an experimental system in which plasmid DNA condensed with basic oligopeptides functions as a model for chromatin. This system reproduces well the yields of DNA radiation damage observed in mammalian cells. We aimed here to extend this model system by including silver nanoparticles. Spectroscopy, light scattering, gel electrophoresis, sedimentation, and atomic force microscopy all indicate that anionic lipoate-coated silver nanoparticles can be co-aggregated with DNA by using a tetra-arginine peptide. The resulting co-aggregates are micron sized, of the same order as the nuclei of mammalian cells. Increasing the ionic strength results in disaggregation enabling recovery of the freed DNA after which it can be subjected to a wide variety of assays to characterize the radiosensitizing effects of the silver nanoparticles. This self-assembled system of three ionically bound components (nanoparticle, DNA, and peptide) offers the advantage of avoiding the complexity of forming and breaking covalent bonds between the nanoparticles and DNA.
期刊介绍:
The objective of the Journal of Nanoparticle Research is to disseminate knowledge of the physical, chemical and biological phenomena and processes in structures that have at least one lengthscale ranging from molecular to approximately 100 nm (or submicron in some situations), and exhibit improved and novel properties that are a direct result of their small size.
Nanoparticle research is a key component of nanoscience, nanoengineering and nanotechnology.
The focus of the Journal is on the specific concepts, properties, phenomena, and processes related to particles, tubes, layers, macromolecules, clusters and other finite structures of the nanoscale size range. Synthesis, assembly, transport, reactivity, and stability of such structures are considered. Development of in-situ and ex-situ instrumentation for characterization of nanoparticles and their interfaces should be based on new principles for probing properties and phenomena not well understood at the nanometer scale. Modeling and simulation may include atom-based quantum mechanics; molecular dynamics; single-particle, multi-body and continuum based models; fractals; other methods suitable for modeling particle synthesis, assembling and interaction processes. Realization and application of systems, structures and devices with novel functions obtained via precursor nanoparticles is emphasized. Approaches may include gas-, liquid-, solid-, and vacuum-based processes, size reduction, chemical- and bio-self assembly. Contributions include utilization of nanoparticle systems for enhancing a phenomenon or process and particle assembling into hierarchical structures, as well as formulation and the administration of drugs. Synergistic approaches originating from different disciplines and technologies, and interaction between the research providers and users in this field, are encouraged.