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

A revolution in novel nanoparticles and colloidal building blocks has been enabled by recent breakthroughs in particle synthesis These new particles are poised to become the ‘atoms’ and ‘molecules’ of tomorrow’s materials if they can be successfully assembled into useful structures Here, we discuss the recent progress made in the synthesis of nanocrystals and colloidal particles and draw analogies between these new particulate building blocks and better-studied molecules and supramolecular objects We argue for a conceptual framework for these new building blocks based on anisotropy attributes and discuss the prognosis for future progress in exploiting anisotropy for materials design and assembly

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Anisotropy of building blocks and their assembly into complex structures

Journal of Physics Condensed Matter: Preface

A challenging goal in materials chemistry and physics is spontaneously to form intended superstructures from designed building blocks. In fields such as crystal engineering and the design of porous materials, this typically involves building blocks of organic molecules, sometimes operating together with metallic ions or clusters. The translation of such ideas to nanoparticles and colloidal-sized building blocks would potentially open doors to new materials and new properties, but the pathways to achieve this goal are still undetermined. Here we show how colloidal spheres can be induced to self-assemble into a complex predetermined colloidal crystal-in this case a colloidal kagome lattice-through decoration of their surfaces with a simple pattern of hydrophobic domains. The building blocks are simple micrometre-sized spheres with interactions (electrostatic repulsion in the middle, hydrophobic attraction at the poles, which we call 'triblock Janus') that are also simple, but the self-assembly of the spheres into an open kagome structure contrasts with previously known close-packed periodic arrangements of spheres. This open network is of interest for several theoretical reasons. With a view to possible enhanced functionality, the resulting lattice structure possesses two families of pores, one that is hydrophobic on the rims of the pores and another that is hydrophilic. This strategy of 'convergent' self-assembly from easily fabricated colloidal building blocks encodes the target supracolloidal architecture, not in localized attractive spots but instead in large redundantly attractive regions, and can be extended to form other supracolloidal networks.

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Directed self-assembly of a colloidal kagome lattice

Controlling interparticle interactions, aggregation and cluster formation is of central importance in a number of areas, ranging from cluster formation in various disease processes to protein crystallography and the production of photonic crystals. Recent developments in the description of the interaction of colloidal particles with short-range attractive potentials have led to interesting findings including metastable liquid-liquid phase separation and the formation of dynamically arrested states (such as the existence of attractive and repulsive glasses, and transient gels). The emerging glass paradigm has been successfully applied to complex soft-matter systems, such as colloid-polymer systems and concentrated protein solutions. However, intriguing problems like the frequent occurrence of cluster phases remain. Here we report small-angle scattering and confocal microscopy investigations of two model systems: protein solutions and colloid-polymer mixtures. We demonstrate that in both systems, a combination of short-range attraction and long-range repulsion results in the formation of small equilibrium clusters. We discuss the relevance of this finding for nucleation processes during protein crystallization, protein or DNA self-assembly and the previously observed formation of cluster and gel phases in colloidal suspensions.

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Equilibrium cluster formation in concentrated protein solutions and colloids

We have conducted two quantitative tests of predictions based on the Halperin-Lubensky-Ma (HLM) theory of fluctuation-induced first-order phase transitions. First, we explore the effect of an external magnetic field on the nematic–smectic-A transition in a liquid crystal. Second, we examine the dependence of the first-order discontinuity as a function of mixture concentration in pure 8CB and three 8CB-10CB mixtures. We find the first quantitative evidence for deviations from the HLM theory.

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Two Experimental Tests of the Halperin-Lubensky-Ma Effect at the Nematic–Smectic- A Phase Transition

We have studied, with quantitative confocal microscopy, epitaxial colloidal crystal growth of particles interacting with an almost hard-sphere (HS) potential in a gravitational field and density matched colloids interacting with a long-range (LR) repulsive potential with a body-centred cubic (BCC) equilibrium crystal phase. We show that in both cases it is possible to grow thick, stacking fault-free metastable crystals: close-packed crystals with any stacking sequence, including hexagonal close packed (HCP), for the HS particles and face-centred cubic (FCC) in the case of the LR colloids. In accordance with recent computer simulations done for HS particles it was found that the optimal lattice constant to grow HS HCP crystals was larger than that of equilibrium FCC crystals. In addition, because of the absence of gravity, pre-freezing could be observed for the particles with the LR potential on a template of charged lines. We also argue that the ability to manipulate colloids with highly focused light, optical traps or tweezers, will become an important tool in both the study of colloidal crystallization and in making new structures. We show how cheap 2D and 3D templates can be made with optical tweezers and demonstrate, in proof of principle experiments with core–shell colloids, how light fields can generate crystal nuclei and other structures in the bulk of concentrated dispersions and how the effect of these structures on the rest of a dispersion can be studied quantitatively in 3D.

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Colloidal epitaxy: playing with the boundary conditions of colloidal crystallization

Ionic microgels are intriguing soft and deformable colloids with an effective pair potential that crosses over from Yukawa-like at large distances to a much softer repulsive interaction at short distances. Here we report the effect of adding an anisotropic dipolar contribution to colloids with such “ultra-soft” interactions. We use an alternating electric field to induce a tunable dipolar contribution, and study the resulting particle self-assembly and phase transitions in situ with confocal laser scanning microscopy. We find significant field-induced structural transitions at low as well as at very high effective volume fractions. At ϕeff = 0.1 we observe a transition from an isotropic to a string fluid. At ϕeff = 0.85, there is a reversible transition from an amorphous to a dipolar crystalline state, followed by the onset of a gas–(string) solid coexistence. At ϕeff = 1.6 and 2.0, i.e. far above close packing, evidence for a field-induced arrested phase separation is found.

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Deformable particles with anisotropic interactions: unusual field-induced structural transitions in ultrasoft ionic microgel colloids

We study the low volume fraction and electric field phase behavior of a Brownian colloidal suspension. On the application of a uniform ac field, we find a novel phase where chains of particles aggregate to form a well defined cellular network, consisting of particle-free "voids" surrounded by a percolating network of particle-rich walls. This cellular structure is stable to very long times, indicative of an equilibrium thermodynamic phase. The cell-cell spacing is not sensitive to the concentration of the sample but scales with sample thickness. Any self-consistent mechanism for the existence of this void phase must consist of long-ranged repulsions and shorter-ranged attractions.

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Low-density ordered phase in brownian dipolar colloidal suspensions.

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Anand Yethiraj

Papers

Two Experimental Tests of the Halperin-Lubensky-Ma Effect at the Nematic–Smectic- A Phase Transition

Colloidal epitaxy: playing with the boundary conditions of colloidal crystallization

Deformable particles with anisotropic interactions: unusual field-induced structural transitions in ultrasoft ionic microgel colloids

Low-density ordered phase in brownian dipolar colloidal suspensions.

Deformable particles with anisotropic interactions: unusual field-induced structural transitions in ultrasoft ionic microgel colloids