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

This critical review provides a processing-structure-property perspective on recent advances in cellulose nanoparticles and composites produced from them. It summarizes cellulose nanoparticles in terms of particle morphology, crystal structure, and properties. Also described are the self-assembly and rheological properties of cellulose nanoparticle suspensions. The methodology of composite processing and resulting properties are fully covered, with an emphasis on neat and high fraction cellulose composites. Additionally, advances in predictive modeling from molecular dynamic simulations of crystalline cellulose to the continuum modeling of composites made with such particles are reviewed (392 references).

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Cellulose nanomaterials review: structure, properties and nanocomposites

Response surface methodology (RSM) as a tool for optimization in analytical chemistry

Self-Assembly of Discrete Cyclic Nanostructures Mediated by Transition Metals

Anion recognition chemistry has grown from its beginnings in the late 1960s with positively charged ammonium cryptand receptors for halide binding to, at the end of the millennium, a plethora of charged and neutral, cyclic and acyclic, inorganic and organic supramolecular host systems for the selective complexation, detection, and separation of anionic guest species. Solvation effects and pH values have been shown to play crucial roles in the overall anion recognition process. More recent developments include exciting advances in anion-templated syntheses and directed self-assembly, ion-pair recognition, and the function of anions in supramolecular catalysis.

Anion Recognition and Sensing: The State of the Art and Future Perspectives

The development of faster, simpler, inexpensive and more environmentally friendly sample-preparation techniques is an important issue in chemical analysis. Recent research trends involve miniaturisation of the traditional liquid-liquid extraction (LLE) principle by greatly reducing the acceptor-to-donor phase ratio. One of the emerging techniques in this area is liquid-phase microextraction (LPME), where a hollow fibre impregnated with an organic solvent is used to accommodate or protect microvolumes of acceptor solution. This novel methodology proved to be an extremely simple, low-cost and virtually solvent-free sample-preparation technique, which provided a high degree of selectivity and enrichment by additionally eliminating the possibility of carry-over between runs. This article presents the different modes and hollow-fibre configurations of LPME, followed by an up-to-date summary of its applications. The most important parameters and practical considerations for method optimisation are also discussed. The article concludes with a comparison of this novel method with solid-phase microextraction (SPME) and single-drop microextraction (SDME).

Developments in liquid-phase microextraction

Chemical oxidation technologies are often employed for the treatment of complex industrial effluents that are not amenable to conventional biological methods. The role of chemical oxidation depends on the treatment objectives and may vary from partial remediation to complete mineralization. In the case of partial treatment, chemical oxidation aims at the selective removal of the more bioresistant fractions and their conversion to readily biodegradable intermediates that can subsequently be treated biologically. Coupling chemical pre-oxidation with biological post-treatment is conceptually beneficial as it can lead to increased overall treatment efficiencies compared with the efficiency of each individual stage. This paper reviews recent developments and highlights some important aspects that need to be addressed when considering such integrated schemes. Copyright © 2004 Society of Chemical Industry

Enhancement of biodegradability of industrial wastewaters by chemical oxidation pre-treatment

The continuous quest for novel sample preparation procedures has led to the development of new methods, whose main advantages are their speed and negligible volume of solvents used. The most recent trends include solvent microextraction, a miniaturisation of the traditional liquid–liquid extraction method, where the solvent to aqueous ratio is greatly reduced. Single-drop microextraction is a methodology that evolved from this approach. It is a simple, inexpensive, fast, effective and virtually solvent-free sample pretreatment technique. This article provides a detailed and updated discussion of the developments, modes and applications of single-drop microextraction, followed by a brief description of the theoretical background of the method. Finally, the most important parameters as well as some practical considerations for method optimisation and development are summarised.

Developments in single-drop microextraction

Vortex-assisted liquid–liquid microextraction of octylphenol, nonylphenol and bisphenol-A

The templating effect of the tetrafluoroborate ion leads to assembly of four CoII ions and six bridging ligands around this anion to give a tetrahedral complex with a bridging ligand along each edge and the anion trapped in the central cavity (shown below). Surprisingly under identical conditions but with NiII a simpler dinuclear complex forms.

Elefteria Psillakis

Papers

Developments in liquid-phase microextraction

Enhancement of biodegradability of industrial wastewaters by chemical oxidation pre-treatment

Developments in single-drop microextraction

Vortex-assisted liquid–liquid microextraction of octylphenol, nonylphenol and bisphenol-A

Anion-Templated Assembly of a Supramolecular Cage Complex.