共查询到11条相似文献，搜索用时 38 毫秒
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方顺燕;宋丹;刘艳萍;徐文娟;刘佳瑶;韩向峙;龙峰 《生物技术通报》2020,(7):228-234
通过融合倏逝波荧光光纤传感器和特异性核酸适配体的优势,提出了一种基于倏逝波荧光原理及其与病原菌尺寸效应的Escherichia coli O157∶H7(E.coli O157∶H7)直接快速检测方法。基本原理是当一定浓度荧光标记E.coli O157∶H7核酸适配体加入样品检测池时,倏逝波激发荧光分子发出荧光,利用倏逝波全光纤生物传感器即可实现荧光信号的定量检测;当荧光标记的核酸适配体与E.coli O157∶H7混合后加入样品检测池,因倏逝波渗入深度仅为100 nm,导致特异性结合E.coli O157∶H7的核酸适配体标记荧光分子不能被激发,从而使得检测荧光信号降低;利用荧光信号强度与E.coli O157∶H7浓度的比例关系即可实现其定量检测。结果表明:该方法检测E.coli O157∶H7的检测限可达610 CFU/mL,线性检测区间为1.1×10～3-1.4×10～7 CFU/mL。实际水样加标回收率在40%-180%之间,相对标准偏差在10%之内,水样基质对E.coli O157∶H7的检测没有明显影响。本研究建立基于倏逝波荧光原理及其与病原菌尺寸效应的生物传感分析方法具有普适性,仅需使用不同荧光标记的生物识别分子即可实现其他病原菌的直接快速检测。 相似文献
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A novel method and instrumental system to determine the total protein concentration in a liquid sample is described. It uses a fiber optic total protein sensor (FOPS) based on the principles of fiber optic evanescent wave spectroscopy. The FOPS applies a dye-immobilized porous glass coating on a multi-mode optical fiber. The evanescent waves at the fiber optic core-cladding interface are used to monitor the protein-induced changes in the sensor element. The FOPS offers a single-step method for quantifying protein concentrations without destroying the sample. The response time and reusability of the FOPS are evaluated. This unique sensing method presents a sensitive and accurate platform for the quantification of protein. 相似文献
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表面质膜共振技术——一种检测蛋白质特异结合反应的方法 总被引：2，自引：0，他引：2
表面质膜共振 (SPR)技术是一种监测生物大分子之间特异结合反应的物理方法。该文综述了SPR技术的特点 ,操作方法 ,光学结构及监测原理 ,数据采集及分析方法 ,应用范围其存在的问题等。同时 ,展望了该技术在昆虫学研究中广阔的应用前景。 相似文献
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We have compiled a comprehensive list of the articles published in the year 2000 that describe work employing commercial optical biosensors. Selected reviews of interest for the general biosensor user are highlighted. Emerging applications in areas of drug discovery, clinical support, food and environment monitoring, and cell membrane biology are emphasized. In addition, the experimental design and data processing steps necessary to achieve high-quality biosensor data are described and examples of well-performed kinetic analysis are provided. 相似文献
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The current understanding of the role of plasma- membrane-associated clathrin suggests that clathrin-coated pits form at the sites of activated receptors and then, following internalization, the clathrin coat is rapidly shed. Utilizing total internal reflection fluorescence microscopy (TIR-FM), we have documented linear lateral motion of cell-surface-associated dsRed-clathrin spots parallel to the plasma membrane. Clathrin spot motility was observed in multiple cell lines (MDCK, CHO, Cos-7 and HeLa). In MDCK cells dsRed-clathrin spots moved along linear pathways up to 4 μm in length with rates of approximately 0.8 μm/s. Spots did not generally undergo internalization during movement. The motion of these puncta was coincident with the microtubule cytoskeleton, and depolymerization of microtubules reduced spot motility over 10-fold. Over-expression of the microtubule-associated protein tau-EGFP decreased spot run length by 40% without affecting the rate of movement. Thus dsRed-clathrin puncta move along the microtubule cytoskeleton parallel to the cell surface. 相似文献
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Silvia Mittler-Neher Jü rgen Spinke Martha Liley Gabriele Nelles Michael Weisser Roberta Back Gerhard Wenz Wolfgang Knoll 《Biosensors & bioelectronics》1995,10(9-10):903-916
Future devices for electronic, photonic or other “intelligent” application involving (bio-) organic materials require nano-fabrication, -manipulation, -patterning and -functionalization techniques. Supramolecular assemblies, aggregates, small molecules and ions have to be controlled with regard to their structure, order and dynamic behaviour down to the molecular or even atomic level.
This contribution summarizes some of our activities aiming at a better understanding of the physical and chemical properties of functionalized and patterned surfaces. We focus on structure/order-property/function relations in such complex systems as interfaces and thin film architectures. Optical techniques (surface plasmon-spectroscopy) as well as surface analytical techniques (cyclic voltammetry and contact angle investigations) are introduced and demonstrated as powerful tools for the characterization of these interfaces and thin films.
Examples will be given covering self-assembly monolayers and molecular recognition—as well as complexation-reactions. 相似文献
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Chapleau RR Blomberg R Ford PC Sagermann M 《Protein science : a publication of the Protein Society》2008,17(4):614-622
Mercury is a ubiquitous pollutant that when absorbed is extremely toxic to a wide variety of biochemical processes. Mercury (II) is a strong, \"invisible\" poison that is rapidly absorbed by tissues of the intestinal tract, kidneys, and liver upon ingestion. In this study, a novel fluorescence-based biosensor is presented that allows for the direct monitoring of the uptake and distribution of the metal under noninvasive in vivo conditions. With the introduction of a cysteine residue at position 205, located in close proximity to the chromophore, the green fluorescent protein (GFP) from Aequorea victoria was converted into a highly specific biosensor for this metal ion. The mutant protein exhibits a dramatic absorbance and fluorescence change upon mercuration at neutral pH. Absorbance and fluorescence properties with respect to the metal concentration exhibit sigmoidal binding behavior with a detection limit in the low nanomolar range. Time-resolved binding studies indicate rapid subsecond binding of the metal to the protein. The crystal structures obtained of mutant eGFP205C indicate a possible access route of the metal into the core of the protein. To our knowledge, this engineered protein is a first example of a biosensor that allows for noninvasive and real-time imaging of mercury uptake in a living cell. A major advantage is that its expression can be genetically controlled in many organisms to enable unprecedented studies of tissue specific mercury uptake. 相似文献
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Gupta V Saharan K Kumar L Gupta R Sahai V Mittal A 《Biotechnology and bioengineering》2008,100(2):284-296
Pseudomonas fluorescens cultures produce fluorescent siderophores. By utilizing optimal conditions for maximizing siderophore production in shake flask cultures of P. fluorescens, we report successful characterization of the culture broth supernatant as a robust ferric ions biosensor. For characterizing the ferric ions biosensor, we tested the effects of pH, buffers, different ferric salts and possible interference by ferrous ions under different solution conditions. We find that the biosensor is very specific to ferric ions only with sensitivity to concentrations as low as 10 microM. Further, the response time of the biosensor is the shortest (approximately 5 min or smaller) for citrate as the accompanying anion with ferric ions. While the response time is longer than that expected of normal biosensors, it is well compensated by the simplicity and economics of the biosensor production. Extremely low standard deviations in several experimental repeats also highlight the robustness of the ferric ions biosensor. Most importantly, the biosensor is extremely easy to use due to its straightforward spectrophotometric applications. We also show the utility of the biosensor with the high resolution technique of fluorescence microscopy. Finally, we report a novel mechanistic finding that siderophores present in the culture broth supernatants have two distinct optically active sites on them, which can be monitored independently in presence or absence of ferric ions. 相似文献