Tag: USC-F0.3-k0.3

Multiswitchable photoacid–hydroxyflavylium–polyelectrolyte nano-assemblies

In the article “Multiswitchable photoacid–hydroxyflavylium–polyelectrolyte nano-assemblies” Alexander Zika and Franziska Gröhn describe the development of a novel reversible multi-switchable system consisting of a cationic polyelectrolyte, a hydroxyflavylium molecule (Flavy), and a photoacid.*

Ternary assemblies with sizes in the hundred-to-few hundred nanometers range in aqueous solution exhibit a multi-addressable size and shape.*

The concept exploits the unique property of the photoacid to form a more highly charged molecule and to switch the Flavy molecule in the same step when excited by light irradiation.*

Due to the network of possible reactions of Flavy, self-assembly can be accessed and triggered in a number of ways.*

While their study focused on the first proof of concept and the relation of molecular and nanoscale switching, a deeper understanding of the molecular binding effects may be considered in future studies.*

The type of the photoacid-based assembly presented in the article bears potential, for example, for delivery where the assembly property changes may provide a desirable transformable platform for tunable and smart transport.*

Atomic force microscopy (AFM) with NanoWorld Ultra-short Cantilevers USC-F0.3-k0.3 in tapping mode was used to investigate the structure.*

Figure 6 from “Multiswitchable photoacid–hydroxyflavylium–polyelectrolyte nano-assemblies” by Alexander Zika and Franziska Gröhn: Comparison of cycle I and cycle II in AFM.

*Alexander Zika and Franziska Gröhn
Multiswitchable photoacid–hydroxyflavylium–polyelectrolyte nano-assemblies
Beilstein J. Org. Chem. 2021, 17, 166–185.
DOI: https://doi.org/10.3762/bjoc.17.17

Please follow this external link to read the full article: https://www.beilstein-journals.org/bjoc/articles/17/17

Open Access : The article “Multiswitchable photoacid–hydroxyflavylium–polyelectrolyte nano-assemblies” by Alexander Zika and Franziska Gröhn is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.

Photoresponsive Photoacid-Macroion Nano-Assemblies

In mother nature, the concept of self-assembly is vital for life, as it generates much of the functionality of living cells. It also bears great synthetic potential for the formation of versatile, switchable, and functional nanostructures.*

Noncovalent interactions can be triggered by external influences, such as the change of pH, light irradiation, thermal activation, introduction of a magnetic field, moisture, or redox response. Of high interest are light-responsive systems, for example in the fields of sensors or therapy, and, thus, it is desirable to explore novel concepts toward light-triggerable self-assembly.*

In the article “Photoresponsive Photoacid-Macroion Nano-Assemblies” Alexander Zika, Sarah Bernhardt and Franziska Gröhn present light-responsive nano-assemblies with light-switchable size based on photoacids.*

Anionic disulfonated napthol derivates and cationic dendrimer macroions are used as building blocks for electrostatic self-assembly. Nanoparticles are already formed under the exclusion of light as a result of electrostatic interactions. Upon photoexcitation, an excited-state dissociation of the photoacidic hydroxyl group takes place, which leads to a more highly charged linker molecule and, subsequently, to a change in size and structure of the nano-assemblies. The effects of the charge ratio and the concentration on the stability have been examined with absorption spectroscopy and -potential measurements.*

The influence of the chemical structure of three isomeric photoacids on the size and shape of the nanoscale aggregates has been studied by dynamic light scattering and atomic force microscopy, revealing a direct correlation of the strength of the photoacid with the changes of the assemblies upon irradiation.*

NanoWorld Ultra-Short AFM Cantilevers of the USC-F0.3-k0.3 type ( typical force constant 0.3 N/m ) were operated in tapping mode for the Atomic Force Microscopy (AFM) images presented in the article.*

Figure 1 a from “Photoresponsive Photoacid-Macroion Nano-Assemblies” by Alexander Zika et al: Assembly formation and photoresponse of the dendrimer–photoacid system at a charge ratio of r = 0.25: (a) AFM height images before (right) and after (left) irradiation. Figure 1 a from “Photoresponsive Photoacid-Macroion Nano-Assemblies” by Alexander Zika et al: Assembly formation and photoresponse of the dendrimer–photoacid system at a charge ratio of r = 0.25: (a) AFM height images before (right) and after (left) irradiation.
Figure 1 a from “Photoresponsive Photoacid-Macroion Nano-Assemblies” by Alexander Zika  et al:
Assembly formation and photoresponse of the dendrimer–photoacid system at a charge ratio of r = 0.25: (a) AFM height images before (right) and after (left) irradiation. Please refer to the full article for the full figure https://www.mdpi.com/2073-4360/12/8/1746

*Alexander Zika, Sarah Bernhardt and Franziska Gröhn
Photoresponsive Photoacid-Macroion Nano-Assemblies
Polymers 2020, 12, 1746
DOI: 10.3390/polym12081746

Please follow this external link to read the full article: https://www.mdpi.com/2073-4360/12/8/1746

Open Access : The article “Photoresponsive Photoacid-Macroion Nano-Assemblies” by Alexander Zika, Sarah Bernhardt and Franziska Gröhn is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Cryopreservation of DNA Origami Nanostructures

Although DNA origami nanostructures have found their way into numerous fields of fundamental and applied research, they often suffer from rather limited stability when subjected to environments that differ from the employed assembly conditions, that is, suspended in Mg2+-containing buffer at moderate temperatures.*

In the article “Cryopreservation of DNA Origami Nanostructures” Yang Xin, Charlotte Kielar, Siqi Zhu, Christoph Sikeler, Xiaodan Xu, Christin Möser, Guido Grundmeier, Tim Liedl, Amelie Heuer-Jungemann, David M. Smith and Adrian Keller investigate means for efficient cryopreservation of 2D and 3D DNA origami nanostructures and, in particular, the effect of repeated freezing and thawing. It is found that, while the 2D DNA origami nanostructures maintain their structural integrity over at least 32 freeze–thaw cycles, ice crystal formation makes the DNA origami gradually more sensitive toward harsh sample treatment conditions. *

The cryoprotectants glycerol and trehalose are found to efficiently protect the DNA origami nanostructures against freeze damage at concentrations between 0.2 × 10−3and 200 × 10−3m and without any negative effects on DNA origami shape. This work thus provides a basis for the long-term storage of DNA origami nanostructures, which is an important prerequisite for various technological and medical applications. *

NanoWorld Ultra-Short Cantilevers for High-Speed AFM USC-F0.3-k0.3 were used for the AFM imaging in liquid of the DNA  origami sample described in this article.

Figure 2 from “Cryopreservation of DNA Origami Nanostructures” by Yang Xin et al.: AFM images of triangular DNA origami nanostructures after 32 freeze–thaw cycles measured a) in air and b) in liquid. AFM images of triangular DNA origami nanostructures assembled from scaffold and staple strands that were subjected to 32 freeze–thaw cycles measured c) in air and d) in liquid. Images have a size of 1.5 × 1.5 μm2 and height scales are 2.3 nm.
Figure 2 from “Cryopreservation of DNA Origami Nanostructures” by Yang Xin et al.:

AFM images of triangular DNA origami nanostructures after 32 freeze–thaw cycles measured a) in air and b) in liquid. AFM images of triangular DNA origami nanostructures assembled from scaffold and staple strands that were subjected to 32 freeze–thaw cycles measured c) in air and d) in liquid. Images have a size of 1.5 × 1.5 μm2 and height scales are 2.3 nm.

*Yang Xin, Charlotte Kielar, Siqi Zhu, Christoph Sikeler, Xiaodan Xu, Christin Möser, Guido Grundmeier, Tim Liedl, Amelie Heuer-Jungemann, David M. Smith and Adrian Keller
Cryopreservation of DNA Origami Nanostructures
Small 2020, 16, 1905959
DOI: 10.1002/smll.20190595

Please follow this external link to read the full article: https://onlinelibrary.wiley.com/doi/pdf/10.1002/smll.201905959

Open Access The article “ Cryopreservation of DNA Origami Nanostructures “ by Yang Xin, Charlotte Kielar, Siqi Zhu, Christoph Sikeler, Xiaodan Xu, Christin Möser, Guido Grundmeier, Tim Liedl, Amelie Heuer-Jungemann, David M. Smith and Adrian Keller is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.