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

Department of Materials Science, University of Patras, 26504 Rio Patras, Greece, Theoretical and Physical Chemistry Institute, National Hellenic Research Foundation, 48 Vass. Constantinou Avenue, 116 35 Athens, Greece, Institut de Biologie Moleculaire et Cellulaire, UPR9021 CNRS, Immunologie et Chimie Therapeutiques, 67084 Strasbourg, France, and Dipartimento di Scienze Farmaceutiche, Universita di Trieste, Piazzale Europa 1, 34127 Trieste, Italy

Chemistry of Carbon Nanotubes

Detection of chemical and biological agents plays a fundamental role in biomedical, forensic and environmental sciences1–4 as well as in anti bioterrorism applications.5–7 The development of highly sensitive, cost effective, miniature sensors is therefore in high demand which requires advanced technology coupled with fundamental knowledge in chemistry, biology and material sciences.8–13

In general, sensors feature two functional components: a recognition element to provide selective/specific binding with the target analytes and a transducer component for signaling the binding event. An efficient sensor relies heavily on these two essential components for the recognition process in terms of response time, signal to noise (S/N) ratio, selectivity and limits of detection (LOD).14,15 Therefore, designing sensors with higher efficacy depends on the development of novel materials to improve both the recognition and transduction processes. Nanomaterials feature unique physicochemical properties that can be of great utility in creating new recognition and transduction processes for chemical and biological sensors15–27 as well as improving the S/N ratio by miniaturization of the sensor elements.28

Gold nanoparticles (AuNPs) possess distinct physical and chemical attributes that make them excellent scaffolds for the fabrication of novel chemical and biological sensors (Figure 1).29–36 First, AuNPs can be synthesized in a straightforward manner and can be made highly stable. Second, they possess unique optoelectronic properties. Third, they provide high surface-to-volume ratio with excellent biocompatibility using appropriate ligands.30 Fourth, these properties of AuNPs can be readily tuned varying their size, shape and the surrounding chemical environment. For example, the binding event between recognition element and the analyte can alter physicochemical properties of transducer AuNPs, such as plasmon resonance absorption, conductivity, redox behavior, etc. that in turn can generate a detectable response signal. Finally, AuNPs offer a suitable platform for multi-functionalization with a wide range of organic or biological ligands for the selective binding and detection of small molecules and biological targets.30–32,36 Each of these attributes of AuNPs has allowed researchers to develop novel sensing strategies with improved sensitivity, stability and selectivity. In the last decade of research, the advent of AuNP as a sensory element provided us a broad spectrum of innovative approaches for the detection of metal ions, small molecules, proteins, nucleic acids, malignant cells, etc. in a rapid and efficient manner.37



Figure 1

Physical properties of AuNPs and schematic illustration of an AuNP-based detection system.



In this current review, we have highlighted the several synthetic routes and properties of AuNPs that make them excellent probes for different sensing strategies. Furthermore, we will discuss various sensing strategies and major advances in the last two decades of research utilizing AuNPs in the detection of variety of target analytes including metal ions, organic molecules, proteins, nucleic acids, and microorganisms.

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Gold nanoparticles in chemical and biological sensing.

Polydopamine and Its Derivative Materials: Synthesis and Promising Applications in Energy, Environmental, and Biomedical Fields

Phenolics are broadly distributed in the plant kingdom and are the most abundant secondary metabolites of plants. Plant polyphenols have drawn increasing attention due to their potent antioxidant properties and their marked effects in the prevention of various oxidative stress associated diseases such as cancer. In the last few years, the identification and development of phenolic compounds or extracts from different plants has become a major area of health- and medical-related research. This review provides an updated and comprehensive overview on phenolic extraction, purification, analysis and quantification as well as their antioxidant properties. Furthermore, the anticancer effects of phenolics in-vitro and in-vivo animal models are viewed, including recent human intervention studies. Finally, possible mechanisms of action involving antioxidant and pro-oxidant activity as well as interference with cellular functions are discussed.

/pdf/plant-phenolics-extraction-analysis-and-their-antioxidant-2ee2ft7zgl.pdf

Plant phenolics: extraction, analysis and their antioxidant and anticancer properties.

The invention discloses a method for measuring aldoketone compounds in tobacco. The method comprises the steps that supercritical fluid is used for extracting the aldoketone compounds in the tobacco, extract liquor is divided into multiple fractions with supercritical fluid chromatography, and each fraction is analyzed with gas chromatography-mass spectrometry. According to the method, the compounds among the separated fractions do not overlap basically, and the problem that the peak capacity of the GC-MS is limited is solved. The result is satisfactory, the quantity of the separated aldoketone compounds is far larger than that of direct injection analysis, and a novel method is provided for measurement of the aldoketone compounds in the tobacco.

Method for measuring aldoketone compounds in tobacco

Based on the impedance behavior of red cell at high frequency, the frequency response of series piezoelectric crystal sensor in the red cell suspension was derived and verified experimentally. A method of using piezoelectric crystal sensor to determine the conductivity of the interior of the cell was proposed. The experimental results show that the mean conductivity of rabbit red cell cytoplasm was 0.269 S/m and the mean shape factor of red cell was 2.05.

Determination of bioelectrochemical parameters of red cell using a piezoelectric crystal sensor

The invention discloses a method for determining ester compounds in tobacco through supercritical fluid chromatography (SFC)-gas chromatography-mass spectrum (GC-MS). According to the method, supercritical fluid is used for extracting ester compounds in tobacco, the extraction fluid is divided into a plurality of segments of fractions through the SFC, and each fraction is analyzed by the GC-MS. The compounds of the separated fractions cannot be overlaid basically, and the problem that the peak capacity of the GC-MS is limited is solved. The result is satisfactory, the number of the separated ester compounds is much larger than that of direct injection analysis, and a novel method is provided for determining ester compounds in tobacco.

Method for determining ester compounds in tobacco through SFC-GC-MS

The composition and activity of the gut microbiota are crucial for health management and disease treatment. Herein, we develop a rapid and robust multichannel sensor array via a recognition engineering strategy using antimicrobial agent (vancomycin, bacitracin, and lysozyme) functional gold nanoclusters and gluconamide-modified Ti3C2 MXenes, which provide superior fingerprint patterns to distinguish gut-derived bacteria. The discrimination ability of the sensor array was highly improved via the synergistic recognition between the bacteria and the various antimicrobial agents. Five gut-derived bacteria, including probiotics, neutral, and pathogenic bacteria were clearly differentiated and discriminated from the bacteria mixtures. Furthermore, the sensing system was successfully applied for the accurate classification of human colorectal cancer samples from healthy individuals rapidly (30 min) with clinically relevant specificity. The rapidity, simplicity, and economic cost of this strategy offers a robust platform for gut microbiota analysis.

Recognition Engineering-Mediated Multichannel Sensor Array for Gut Microbiota Sensing.

A modified algorithm, the iterative Kalman filter, for the analysis of enzymic kinetic data was investigated and successfully applied to the determination of urea in human blood by a urease catalytic reaction. This reaction was monitored with a novel sensor, the surface acoustic wave enzyme sensor system recently proposed by our laboratory. The results were compared with those provided by a calibration graph and classical colorimetry methods. In contrast to these conventional methods, the iterative extended-Kalman filter is shown to be an excellent data analysis method for enzyme kinetic analysis. The urease kinetic parameters were also estimated according to the iterative Kalman filtering results.

Shouzhuo Yao

Papers

Method for measuring aldoketone compounds in tobacco

Determination of bioelectrochemical parameters of red cell using a piezoelectric crystal sensor

Method for determining ester compounds in tobacco through SFC-GC-MS

Recognition Engineering-Mediated Multichannel Sensor Array for Gut Microbiota Sensing.

Study on a modified algorithm—iterative Kalman filter and its application in enzymic kinetics