Measuring of Binding kinetics of biomolecular interactions Using a Localized Surface Plasmon Couple Fluorescence Fiber-Optic Biosensor

被引:0
作者
Chang, Ying-Feng [1 ,2 ]
Hsieh, Jo-Ping [1 ,2 ,4 ]
Su, Li-Chen [2 ,3 ]
Li, Ying-Chang [2 ,3 ]
Lee, Cheng-Chung [3 ]
Chou, Chien [1 ,2 ,3 ]
机构
[1] Natl Yang Ming Univ, Inst Biophoton, Taipei 112, Taiwan
[2] Chang Gung Univ, Grad Inst Electroopt Engn, Taoyuan 333, Taiwan
[3] Natl Cent Univ, Dept Opt & Photon, Taoyuan 320, Taiwan
[4] Chang Gung Univ, Chang Gung Mol Med Res Ctr, Taoyuan 333, Taiwan
来源
BIOSENSING III | 2010年 / 7759卷
关键词
binding kinetics; localized surface plasmon; fiber-optic biosensor; QUARTZ-CRYSTAL BIOSENSOR; PROTEIN; ALPHA;
D O I
10.1117/12.863621
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
In this study, we describe a novel method for analyzing protein-protein binding kinetics at ultra-low concentration (1 pg/mL) using a localized surface plasmon coupled fluorescence fiber-optic biosensor (LSPCF-FOB). The association and dissociation rate constants, ka and kd, respectively, for the binding kinetics of the mouse IgG/ anti-mouse IgG interaction have been calculated to be ka = (5.9928 +/- 3.1540) x 10(6) M(-1)s(-1) and kd = (1.0587 +/- 0.5572) x 10(-3) s(-1). The theoretical basis of this analytical approach is a rapid-mixing model integrated with a two-compartment model; has been experimentally verified in this study as well. The LSPCF-FOB provides a potentially alternative option for characterizing the interaction of biomolecules at ultra-low concentrations.
引用
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页数:6
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