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

基礎講座 電気泳動(Electrophoresis)

Micro total analysis systems. Latest advancements and trends.

Accurate and high throughput cell sorting is a critical enabling technology in molecular and cellular biology, biotechnology, and medicine While conventional methods can provide high efficiency sorting in short timescales, advances in microfluidics have enabled the realization of miniaturized devices offering similar capabilities that exploit a variety of physical principles We classify these technologies as either active or passive Active systems generally use external fields (eg, acoustic, electric, magnetic, and optical) to impose forces to displace cells for sorting, whereas passive systems use inertial forces, filters, and adhesion mechanisms to purify cell populations Cell sorting on microchips provides numerous advantages over conventional methods by reducing the size of necessary equipment, eliminating potentially biohazardous aerosols, and simplifying the complex protocols commonly associated with cell sorting Additionally, microchip devices are well suited for parallelization, enabling complete lab-on-a-chip devices for cellular isolation, analysis, and experimental processing In this review, we examine the breadth of microfluidic cell sorting technologies, while focusing on those that offer the greatest potential for translation into clinical and industrial practice and that offer multiple, useful functions We organize these sorting technologies by the type of cell preparation required (ie, fluorescent label-based sorting, bead-based sorting, and label-free sorting) as well as by the physical principles underlying each sorting mechanism

Microfluidic cell sorting: a review of the advances in the separation of cells from debulking to rare cell isolation

Optofluidics - the synergistic integration of photonics and microfluidics - has recently emerged as a new analytical field that provides a number of unique characteristics for enhanced sensing performance and simplification of microsystems. In this review, we describe various optofluidic architectures developed in the past five years, emphasize the mechanisms by which optofluidics enhances bio/chemical analysis capabilities, including sensing and the precise control of biological micro/nanoparticles, and envision new research directions to which optofluidics leads.

/pdf/optofluidic-microsystems-for-chemical-and-biological-2x1od0syk0.pdf

Optofluidic microsystems for chemical and biological analysis

Effective methods for manipulating, isolating and sorting cells and particles are essential for the development of microfluidic-based life science research and diagnostic platforms. We demonstrate an integrated optical platform for cell and particle sorting in microfluidic structures. Fluorescent-dyed particles are excited using an integrated optical waveguide network within micro-channels. A diode-bar optical trapping scheme guides the particles across the waveguide/micro-channel structures and selectively sorts particles based upon their fluorescent signature. This integrated detection and separation approach streamlines microfluidic cell sorting and minimizes the optical and feedback complexity commonly associated with extant platforms.

/pdf/microfluidic-sorting-system-based-on-optical-waveguide-54yh4xios1.pdf

Microfluidic sorting system based on optical waveguide integration and diode laser bar trapping

We demonstrate a new technique for trapping, sorting, and manipulating cells and micrometer-sized particles within microfluidic systems, using a diode laser bar. This approach overcomes the scaling limitations of conventional scanned laser traps, while avoiding the computational and optical complexity inherent to holographic optical trapping schemes. The diode laser bar enables us to control a large trapping zone, 1 microm by 100 microm, without the necessity of scanning or altering the phase of the beam.

Optical trapping, manipulation, and sorting of cells and colloids in microfluidic systems with diode laser bars.

Hydrodynamic focusing has proven to be a useful microfluidics technique for the study of systems under rapid mixing conditions. Most studies to date have used a “push” configuration, requiring multiple pumps or pressure sources that complicate implementation and limit applications in point-of-care environments. Here, we demonstrate a simplified hydrodynamic focusing approach, in which a single pump pulling at the device outlet can be used to drive hydrodynamic focusing with not only excellent control over the focus width and stream velocity, but also with minimal sample consumption. In this technique, flow can be either mechanically driven or induced simply through capillarity.

Hydrodynamic focusing for vacuum-pumped microfluidics

Advantages of performing analytical and diagnostic tasks in microfluidic-based systems include small sample volume requirements, rapid transport times and the promise of compact, portable instrumentation. The application of such systems in home and point-of-care situations has been limited, however, because these devices typically require significant associated hardware to initiate and control fluid flow. Capillary-based pumping can address many of these deficiencies by taking advantage of surface tension to pull fluid through devices. The development of practical instrumentation however will rely upon the development of precision control schemes to complement capillary pumping. Here, we introduce a straightforward, robust approach that allows for reconfigurable fluid guidance through otherwise fixed capillary networks. This technique is based on the opening and closing of microfluidic channels cast in a flexible elastomer via automated or even manual mechanical actuation. This straightforward approach can completely and precisely control flows such as samples of complex fluids, including whole blood, at very high resolutions according to real-time user feedback. These results demonstrate the suitability of this technique for portable, microfluidic instruments in laboratory, field or clinical diagnostic applications.

https://iopscience.iop.org/article/10.1088/0960-1317/14/11/010/pdf

Flow control for capillary-pumped microfluidic systems

Control of relative flow resistance is used for the actuation of both one- and two-input microfluidic “logical gates”. By taking advantage of system nonlinearities and despite the linear response of laminar flows associated with these length scales, a number of operators including the NOT, AND, OR, XOR, NOR, and NAND are demonstrated. Because these gates can be actuated simultaneously they can be combined to form more complicated devices such as a half adder. This approach is therefore flexible and illustrates that any macro- or microscale technique that can alter flow resistance can be used as the basis of a fluid-based logical micro-operator.

Tor Vestad

Papers

Microfluidic sorting system based on optical waveguide integration and diode laser bar trapping

Optical trapping, manipulation, and sorting of cells and colloids in microfluidic systems with diode laser bars.

Hydrodynamic focusing for vacuum-pumped microfluidics

Flow control for capillary-pumped microfluidic systems

Flow resistance for microfluidic logic operations