抗原变异可使得多种致病微生物易于逃避宿主免疫应答。表达在感染红细胞表面的恶性疟原虫红细胞表面蛋白1（PfPMP1）与感染红细胞、内皮细胞、树突状细胞以及胎盘的单个或多个受体作用，在黏附及免疫逃避中起关键的作用。每个单倍体基因组var基因家族编码约60种成员，通过启动转录不同的var基因变异体为抗原变异提供了分子基础。

疟原虫var基因转换速率变化导致抗原变异[英]／Paul H, Robert P, Christodoulou Z, et al//Proc Natl Acad Sci U S A

http://pharmaquest.weebly.com/uploads/9/9/4/2/9942916/superparamagnetic_iron_oxide_nanoparticles_spions.pdf

Superparamagnetic iron oxide nanoparticles (SPIONs): Development, surface modification and applications in chemotherapy

The magnetization of a magnetic material can be reversed by using electric currents that transport spin angular momentum. In the reciprocal process a changing magnetization orientation produces currents that transport spin angular momentum. Understanding how these processes occur reveals the intricate connection between magnetization and spin transport, and can transform technologies that generate, store or process information via the magnetization direction. Here we explain how currents can generate torques that affect the magnetic orientation and the reciprocal effect in a wide variety of magnetic materials and structures. We also discuss recent state-of-the-art demonstrations of current-induced torque devices that show great promise for enhancing the functionality of semiconductor devices.

https://physics.nyu.edu/kentlab/Papers/2012/NatureMaterials_11_372_2012.pdf

Current-induced torques in magnetic materials

Iron-based microstructured or nanostructured materials, including Fe, γ-Fe2O3, and Fe3O4, are highly desirable for magnetic applications because of their high magnetization and a wide range of magnetic anisotropy. An important application of these materials is use as an electromagnetic wave absorber to absorb radar waves in the centimeter wave (2−18 GHz). Dendrite-like microstructures were achieved with the phase transformation from dendritic α-Fe2O3 to Fe3O4, Fe by partial and full reduction, and γ-Fe2O3 by a reduction−oxidation process, while still preserving the dendritic morphology. The investigation of the magnetic properties and microwave absorbability reveals that the three hierarchical microstructures are typical ferromagnets and exhibit excellent microwave absorbability. In addition, this also confirms that the microwave absorption properties are ascribed to the dielectric loss for Fe and the combination of dielectric loss and magnetic loss for Fe3O4 and γ-Fe2O3.

Hierarchical Dendrite-Like Magnetic Materials of Fe3O4, γ-Fe2O3, and Fe with High Performance of Microwave Absorption

Iron carbide nanoparticles have long been considered to have great potential in new energy conversion, nanomagnets, and nanomedicines. However, the conventional relatively harsh synthetic conditions of iron carbide hindered its wide applications. In this article, we present a facile wet-chemical route for the synthesis of Hagg iron carbide (Fe5C2) nanoparticles, in which bromide was found to be the key inducing agent for the conversion of Fe(CO)5 to Fe5C2 in the synthetic process. Furthermore, the as-synthesized Fe5C2 nanoparticles were applied in the Fischer–Tropsch synthesis (FTS) and exhibited intrinsic catalytic activity in FTS, demonstrating that Fe5C2 is an active phase for FTS. Compared with a conventional reduced-hematite catalyst, the Fe5C2 nanoparticles showed enhanced catalytic performance in terms of CO conversion and product selectivity.

Fe5C2 nanoparticles: a facile bromide-induced synthesis and as an active phase for Fischer-Tropsch synthesis.

We present an innovative approach to the production of single-crystal iron oxide nanorings employing a solution-based route. Single-crystal hematite (alpha-Fe2O3) nanorings were synthesized using a double anion-assisted hydrothermal method (involving phosphate and sulfate ions), which can be divided into two stages: (1) formation of capsule-shaped alpha-Fe2O3 nanoparticles and (2) preferential dissolution along the long dimension of the elongated nanoparticles (the c axis of alpha-Fe2O3) to form nanorings. The shape of the nanorings is mainly regulated by the adsorption of phosphate ions on faces parallel to c axis of alpha-Fe2O3 during the nanocrystal growth, and the hollow structure is given by the preferential dissolution of the alpha-Fe2O3 along the c axis due to the strong coordination of the sulfate ions. By varying the ratios of phosphate and sulfate ions to ferric ions, we were able to control the size, morphology, and surface architecture to produce a variety of three-dimensional hollow nanostructures. These can then be converted to magnetite (Fe3O4) and maghemite (gamma-Fe2O3) by a reduction or reduction-oxidation process while preserving the same morphology. The structures and magnetic properties of these single-crystal alpha-Fe2O3, Fe3O4, and gamma-Fe2O3 nanorings were characterized by various analytical techniques. Employing off-axis electron holography, we observed the classical single-vortex magnetic state in the thin magnetite nanorings, while the thicker rings displayed an intriguing three-dimensional magnetic configuration. This work provides an easily scaled-up method for preparing tailor-made iron oxide nanorings that could meet the demands of a variety of applications ranging from medicine to magnetoelectronics.

/pdf/large-scale-synthesis-of-single-crystalline-iron-oxide-45ui295gcp.pdf

Large-scale synthesis of single-crystalline iron oxide magnetic nanorings.

Using transmission electron microscopy, we investigate the thermally activated motion of domain walls (DWs) between two positions in Permalloy (Ni80Fe20) nanowires at room temperature. We show that this purely thermal motion is well described by an Arrhenius law, allowing for a description of the DW as a quasiparticle in a one-dimensional potential landscape. By injecting small currents, the potential is modified, allowing for the determination of the nonadiabatic spin torque: beta(t) = 0.010 +/- 0.004 for a transverse DW and beta(v) = 0.073 +/- 0.026 for a vortex DW. The larger value is attributed to the higher magnetization gradients present.

/pdf/nonadiabatic-spin-torque-investigated-using-thermally-2mnix8h99v.pdf

Nonadiabatic spin torque investigated using thermally activated magnetic domain wall dynamics.

The correlation between magnetic spin structure and geometry in nanoscale chemically synthesized Fe3O4 rings has been investigated by transmission electron microscopy. We find primarily the flux closure vortex states but in rings with thickness variations, an effective stray field occurs. Using tomography, we determine the complete three-dimensional geometries of thicker rings. A direct correlation between the geometry and the magnetization which points out of plane in the thickest parts of the ring yielding an intermediate magnetic state between the vortex state and the tube state is found. The interaction between exchange coupled rings leads to antiparallel vortex states and extended onion states.

/pdf/correlation-between-magnetic-spin-structure-and-the-three-xtp6axx2fi.pdf

Matthias Eltschka

Papers

Large-scale synthesis of single-crystalline iron oxide magnetic nanorings.

Nonadiabatic spin torque investigated using thermally activated magnetic domain wall dynamics.

Correlation between magnetic spin structure and the three-dimensional geometry in chemically synthesized nanoscale magnetite rings