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A fractal analysis of pathogen detection by biosensors

机译:生物传感器检测病原体的分形分析

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摘要

A fractal analysis is presented for the detection of pathogens such as Franscisela tularensis, Yersinia pestis (the bacterium that causes plague), Bacillus anthracis, Venezuelan equine encephalitis (VEE) virus, Vavcinia virus, and Escherichia coli using a cellular analysis and notification of antigens risks and yields (CANARY) biosensor [T.H. Rider, M.S. Petrovic, F.E. Nargi, J.D Harper, E.D. Schwoebel, R.H. Mathews, D.J. Blanchard, L.T Bortolin, A.M. Young, J. Chen, M.A. Hollis, A cell-based sensor for rapid identification of pathogens, Science 301 (2003, 11 July) 213-215, T.H. Rider, M.S. Petrovic, F.E. Nargi, J.D. Harper, E.D. Schwoebel, R.H. Mathews, D.J. Blanchard, L.T. Bortolin, A.M. Young, J. Chen, M.A. Hollis, A cell-based sensor for rapid identification of pathogens, Science 301 (2003, 11 July) 213-215. Science Online, www.sciencemag.org/cgi/content/full/031/5630/213/DC1]. In general, the binding and dissociation rate coefficients may be adequately described by either a single- or a dual-fractal analysis. An attempt is made to relate the binding rate coefficient to the degree of heterogeneity (fractal dimension value) present on the biosensor surface. Binding and dissociation rate coefficient values obtained are presented.Due to the dilute nature of the analyte(s) present, in some cases, a triple-fractal analysis is required to adequately describe the binding kinetics. It should be noted, and this is not entirely unexpected, that there is a lot of variation in the original experimental data when dilute concentrations of the analyte were analyzed by the CANARY biosensor [T.H. Rider, M.S. Petrovic, F.E. Nargi, J.D Harper, E.D. Schwoebel, R.H. Mathews, D.J. Blanchard, L.T Bortolin, A.M. Young, J. Chen, M.A. Hollis, A cell-based sensor for rapid identification of pathogens, Science 301 (2003, 11 July) 213-215, Science Online, www.sciencemag.org/cgi/content/ftill/031/5630/213/DC1]. The data analyzed in this manuscript appears smoother since only discrete points at different time intervals were analyzed. The kinetics aspects along with the affinity values presented are of interest and should along with the rate coefficients presented for the binding and the dissociation phase be of significant interest in help designing better biosensors for an application area that is bound to gain increasing importance in the future. (C) 2004 Elsevier B.V. All rights reserved.
机译:分形分析提出了一种病原体检测方法,可通过细胞分析和抗原通知来检测病原体,例如弗兰西斯图拉菌,鼠疫耶尔森氏菌(引起鼠疫的细菌),炭疽杆菌,委内瑞拉马脑炎(VEE)病毒,痘苗病毒和大肠埃希氏菌风险和收益(CANARY)生物传感器[TH骑手,M.S.彼得罗维奇(Petrovic),纳吉(Nargi),哈珀(J.D. Schwoebel,R.H. Mathews,D.J.布兰查德(L.T.)布兰查德(L.T. Bortolin),上午Young,J. Chen,M.A. Hollis,一种用于快速识别病原体的基于细胞的传感器,科学301(2003,7月11日)213-215,T.H.骑手,M.S.彼得罗维奇(Petrovic),纳吉(Nargi),哈珀(J.D. Schwoebel,R.H. Mathews,D.J. L.T.布兰查德博尔托林Young,J. Chen,M.A. Hollis,一种用于快速识别病原体的基于细胞的传感器,科学301(2003,7月11日)213-215。科学在线,www.sciencemag.org / cgi / content / full / 031/5630/213 / DC1]。通常,结合和解离速率系数可以通过单分形或双分形分析来充分描述。尝试将结合速率系数与生物传感器表面上存在的异质程度(分数维值)相关联。给出了获得的结合和解离速率系数值。由于存在的被分析物的稀性,在某些情况下,需要进行三次分形分析才能充分描述结合动力学。应当指出的是,这并不是完全出乎意料的,当通过CANARY生物传感器分析稀浓度的分析物时,原始实验数据会有很多变化。骑手,M.S.彼得罗维奇(Petrovic),纳吉(Nargi),哈珀(J.D. Schwoebel,R.H. Mathews,D.J.布兰查德(L.T.)布兰查德(L.T. Bortolin),上午Young,J。Chen,MA Hollis,一种用于快速识别病原体的基于细胞的传感器,Science 301(2003年7月11日)213-215,Science Online,www.sciencemag.org / cgi / content / ftill / 031/5630 / 213 / DC1]。由于仅分析了不同时间间隔的离散点,因此本手稿中分析的数据显得更平滑。动力学方面的问题以及提出的亲和力值是有意义的,并且应该为结合和解离阶段提出的速率系数也很重要,有助于为将来必将越来越重要的应用领域设计更好的生物传感器。 。 (C)2004 Elsevier B.V.保留所有权利。

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