Institute for Molecules and Materials, Radboud University Nijmegen, Heyendaalseweg 135, 6525 AJ, Nijmegen, The Netherlands.
ACS Nano. 2011 Aug 23;5(8):6394-402. doi: 10.1021/nn201571y. Epub 2011 Jul 15.
Protein cages such as ferritin and viral capsids are interesting building blocks for nanotechnology due to their monodisperse structure and ability to encapsulate various functional moieties. Here we show that recombinant ferritin protein cages encapsulating Fe(3)O(4)-γ-Fe(2)O(3) iron oxide (magnetoferritin) nanoparticles and photodegradable Newkome-type dendrons self-assemble into micrometer-sized complexes with a face-centered-cubic (fcc) superstructure and a lattice constant of 13.1 nm. The magnetic properties of the magnetoferritin particles are affected directly by the hierarchical organization. Magnetoferritin nanoparticles dispersed in water exhibit typical magnetism of single domain noninteracting nanoparticles; however, the same nanoparticles organized into fcc superstructures show clearly the effects of the altered magnetostatic (e.g., dipole-dipole) interactions by exhibiting, for example, different hysteresis of the field-dependent magnetization. The magnetoferritin-dendron assemblies can be efficiently disassembled by a short optical stimulus resulting in release of free magnetoferritin particles. After the triggered release the nanomagnetic properties of the pristine magnetoferritin nanoparticles are regained.
由于其单分散结构和封装各种功能部分的能力,蛋白质笼如铁蛋白和病毒衣壳是纳米技术的有趣构建块。在这里,我们展示了包封 Fe(3)O(4)-γ-Fe(2)O(3) 氧化铁(磁铁蛋白)纳米颗粒的重组铁蛋白蛋白笼和可光降解的 Newkome 型树枝状大分子自组装成具有面心立方(fcc)超结构和晶格常数为 13.1nm 的微米级复合物。磁铁蛋白颗粒的磁性直接受到分级组织的影响。分散在水中的磁铁蛋白纳米颗粒表现出典型的单畴非相互作用纳米颗粒的磁性;然而,相同的纳米颗粒组织成 fcc 超结构通过表现出例如磁场依赖性磁化的不同滞后,清楚地显示出改变的静磁(例如偶极-偶极)相互作用的影响。磁铁蛋白-树枝状大分子组装体可以通过短的光学刺激有效地解离,从而释放游离的磁铁蛋白颗粒。触发释放后,原始磁铁蛋白纳米颗粒的纳米磁性得以恢复。
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